97 results on '"Gourtsoyianni S."'
Search Results
2. Association of dynamic contrast-enhanced MRI and 18F-Fluorodeoxyglucose PET/CT parameters with neoadjuvant therapy response and survival in esophagogastric cancer
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Withey, Samuel J., primary, Owczarczyk, Kasia, additional, Grzeda, Mariusz T., additional, Yip, Connie, additional, Deere, Harriet, additional, Green, Mike, additional, Maisey, Nick, additional, Davies, Andrew R., additional, Cook, Gary J., additional, Goh, Vicky, additional, Baker, C.R., additional, Bell, J., additional, Chang, F., additional, Chicklore, S., additional, Cominos, M., additional, Coombes, A., additional, Dunn, J.N., additional, George, S., additional, Gill-Barman, B., additional, Gossage, J.A., additional, Gourtsoyianni, S., additional, Green, A., additional, Griffin, N., additional, Hill, M., additional, Hynes, O., additional, Iezzi, C., additional, Jacques, A., additional, Kelly, M., additional, Mahadeva, U., additional, McEwan, R., additional, Meenan, J., additional, Neji, R., additional, Ngan, S., additional, Padormo, F., additional, Qureshi, A., additional, Reyhani, A., additional, Sharkey, A.R., additional, Spence, J., additional, Subesinghe, M., additional, Tham, G., additional, Waters, J., additional, and Zeki, S.S., additional
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- 2023
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3. Outcomes of double balloon enteroscopy on patients with Peutz-Jeghers syndrome who missed surveillance
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Stasinos, I., additional, Poutakidis, C., additional, Zantza, P. S., additional, Gourtsoyianni, S., additional, Androne, I., additional, Sidiropoulos, O., additional, Braimakis, I., additional, Leventaki, F., additional, Theofanopoulou, A., additional, Tsibouris, P., additional, Kalantzis, C., additional, Floros, D., additional, and Apostolopoulos, P., additional
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- 2023
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4. Rectal tumour volume (GTV) delineation using T2-weighted and diffusion-weighted MRI: Implications for radiotherapy planning
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Regini, F., Gourtsoyianni, S., Cardoso De Melo, R., Charles-Edwards, G.D., Griffin, N., Parikh, J., Rottenberg, G., Leslie, M., Gaya, A., and Goh, V.
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- 2014
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5. Comparison between 1.5-T and 3.0-T MRI for the diagnosis of placenta accreta spectrum disorders
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Bourgioti, C. Zafeiropoulou, K. Tzavara, C. Daskalakis, G. Fotopoulos, S. Theodora, M. Nikolaidou, M.E. Konidari, M. Gourtsoyianni, S. Panourgias, E. Koutoulidis, V. Martzoukos, E.A. Konstantinidou, A.E. Moulopoulos, L.A.
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Purpose: Accurate antenatal diagnosis of placenta accreta spectrum (PAS) is important for optimal management. The purpose of this study was to compare the respective capabilities of 1.5-T and 3.0-T MRI in the diagnosis of PAS. Materials and methods: Between March 2016-March 2021, 190 pregnant women at high risk for PAS underwent dedicated prenatal MRI with either 1.5-T or 3.0-T units at a tertiary imaging center. Cesarian section and MRI were performed less than 6 weeks from each other. Prospectively collected data were evaluated by two experienced genitourinary radiologists for presence and extent of PAS. A comparative study was designed to investigate differences in predictive ability between 1.5-T and 3.0-T MRI groups. Sensitivity, specificity, accuracy, negative and positive prognostic values relative to intraoperative/histological findings, were computed for both groups and were compared with chi-square (χ 2) test. Interobserver agreement was estimated using Kappa test. Results: One hundred-eighty-two gravid women were included in the study; of these, 91/182 (50%) women were evaluated with 1.5-T (mean age, 35 ± 5.1 [SD] years; mean gestational age: 32.5 weeks) and 91/182 (50%) with 3.0-T MRI (mean age, 34.9 ± 4.9 [SD] years; mean gestational age, 32.1 weeks). 1.5-T MRI yielded 95.7% sensitivity (95% CI: 87.8–99.1) and 81.8% specificity (95% CI: 59.8) and 3.0-T MRI 93.8% sensitivity (95% CI: 86.0–97.9) and 83.3% specificity (95% CI: 48.2–97.7) for PAS identification, with no differences between the two groups (P = 0.725 and P >0.999, respectively). MRI showed excellent predictive ability for detecting extrauterine placental spread with 100% sensitivity (95% CI: 89.4–100.0), 96.7% specificity (95% CI: 88.1–99.6) for 1.5-T and 97% sensitivity (95% CI: 84.2–99.9), 96.7% specificity (95% CI: 88.1–99.6) for 3.0-T without differences between the two groups (P > 0.999). Interobserver agreement was excellent for both groups. The most frequently detected MRI signs of PAS for both 1.5-T and 3.0-T groups were placental heterogeneity (n = 85, 93.5% vs. n = 90, 98.9%; P = 0.413), and intraplacental fetal vessels (n = 64, 70.3% vs. n = 65, 71.4%; P = 0.870). Conclusion: This study suggests that 3.0-T MRI and 1.5-T MRI are equivalent for the diagnosis of PAS. © 2022 Société française de radiologie
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- 2022
6. MRI at the completion of chemoradiotherapy can accurately evaluate the extent of disease in women with advanced urethral carcinoma undergoing anterior pelvic exenteration
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Gourtsoyianni, S., Hudolin, T., Sala, E., Goldman, D., Bochner, B.H., and Hricak, Hedvig
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- 2011
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7. MRI of anal cancer: assessing response to definitive chemoradiotherapy
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Gourtsoyianni, S. and Goh, V.
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- 2014
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8. Management of the adenocarcinoma of the upper rectum: a reappraisal
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Pechlivanides, G. Gourtsoyianni, S. Gouvas, N. Sougklakos, J. Xynos, E.
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The present review attempts to assess whether upper rectal cancer (URC) should be treated either as colon cancer or as rectal one, namely to be managed with upfront surgery without neo-adjuvant treatment and partial mesorectal excision (PME), or with neo-adjuvant short course radiotherapy (SCRT) or chemoradiotherapy (CRT) as indicated, followed by surgery with total mesorectal excision. Reports from current evidence including studies, reviews and various guidelines are conflicting. Main reasons for inability to reach safe conclusions are (i) the various anatomical definitions of the rectum and its upper part, (ii) the inadequate preoperative local staging,(iii) the heterogeneity of selection criteria for the neo-adjuvant treatment,(iv) the different neo-adjuvant treatment regimens, and(v) the variety in the extent of surgical resection, among the studies. Although not adequately supported, locally advanced URC can be treated with neo-adjuvant CRT provided the lesion is within the radiation field of safety, and a PME if the lower border of the tumour is located above the anterior peritoneal reflection. There is evidence that adjuvant chemotherapy is of benefit in high-risk stage II and stage III lesions. © 2020, Italian Society of Surgery (SIC).
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- 2021
9. Hellenic society of medical oncology (HESMO) guidelines for the management of anal cancer
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Gouvas, N. Gourtsoyianni, S. Kalogeridi, M.A. Sougklakos, J. Vini, L. Xynos, E. the Hellenic Society of Medical Oncology (HESMO)
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Despite considerable improvement in the management of anal cancer, there is a great deal of variation in the outcomes among European countries, and in particular among different hospital centres in Greece and Cyprus. The aim was to elaborate a consensus on the multidisciplinary management of anal cancer, based on European guidelines (European Society of Medical Oncologists-ESMO), considering local special characteristics of our healthcare system. Following discussion and online communication among members of an executive team, a consensus was developed. Guidelines are proposed along with algorithms of diagnosis and treatment. The importance of centralisation, care by a multidisciplinary team (MDT) and adherence to guidelines are emphasised. © 2020, Italian Society of Surgery (SIC).
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- 2021
10. Imaging during pregnancy: What the radiologist needs to know
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Bourgioti, C. Konidari, M. Gourtsoyianni, S. Moulopoulos, L.A.
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reproductive and urinary physiology - Abstract
During the last decades, there has been a growing demand for medical imaging in gravid women. Imaging of the pregnant woman is challenging as it involves both the mother and the fetus and, consequently, several medical, ethical, or legal considerations are likely to be raised. Theoretically, all currently available imaging modalities may be used for the evaluation of the pregnant woman; however, in practice, confusion regarding the safety of the fetus often results in unnecessary avoidance of useful diagnostic tests, especially those involving ionizing radiation. This review article is focused on the current safety guidelines and considerations regarding the use of different imaging modalities in the pregnant population; also presented is an imaging work-up for the most common medical conditions of pregnant women, with emphasis on fetal and maternal safety. © 2021 Société française de radiologie
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- 2021
11. Involvement of radiologists in oncologic multidisciplinary team meetings: an international survey by the European Society of Oncologic Imaging
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Neri, E. Gabelloni, M. Bäuerle, T. Beets-Tan, R. Caruso, D. D’Anastasi, M. Dinkel, J. Fournier, L.S. Gourtsoyianni, S. Hoffmann, R.-T. Mayerhöfer, M.E. Regge, D. Schlemmer, H.P. Laghi, A.
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education - Abstract
Objectives: Multidisciplinary tumour boards (MTBs) play an increasingly important role in managing cancer patients from diagnosis to treatment. However, many problems arise around the organisation of MTBs, both in terms of organisation-administration and time management. In this context, the European Society of Oncologic Imaging (ESOI) conducted a survey among its members, aimed at assessing the quality and amount of involvement of radiologists in MTBs, their role in it and related issues. Methods: All members were invited to fill in a questionnaire consisting of 15 questions with both open and multiple-choice answers. Simple descriptive analyses and graphs were performed. Results: A total of 292 ESOI members in full standing for the year 2018 joined the survey. Most respondents (89%) declared to attend MT-Bs, but only 114 respondents (43.9%) review over 70% of exams prior to MTB meetings, mainly due to lack of time due to a busy schedule for imaging and reporting (46.6%). Perceived benefits (i.e. surgical and histological feedback (86.9%), improved knowledge of cancer treatment (82.7%) and better interaction between radiologists and referring clinicians for discussing rare cases (56.9%)) and issues (i.e. attending MTB meetings during regular working hours (71.9%) and lack of accreditation with continuing medical education (CME) (85%)) are reported. Conclusions: Despite the value and benefits of radiologists’ participation in MTBs, issues like improper preparation due to a busy schedule and no counterpart in CME accreditation require efforts to improve the role of radiologists for a better patient care. Key Points: • Most radiologists attend multidisciplinary tumour boards, but less than half of them review images in advance, mostly due to time constraints. • Feedback about radiological diagnoses, improved knowledge of cancer treatment and interaction with referring clinicians are perceived as major benefits. • Concerns were expressed about scheduling multidisciplinary tumour boards during regular working hours and lack of accreditation with continuing medical education. © 2020, The Author(s).
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- 2021
12. Standardisation of liver MDCT by tracking liver parenchyma enhancement to trigger imaging
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Brodoefel, H., Tognolini, A., Zamboni, G. A., Gourtsoyianni, S., Claussen, C. D., and Raptopoulos, V.
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- 2012
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13. Air trapping in Wegener’s granulomatosis: an additional finding on expiratory chest HRCT
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Magkanas, E., Detorakis, E., Nikolakopoulos, I., Gourtsoyianni, S., Linardakis, M., Sidiropoulos, P., Boumpas, D., and Gourtsoyiannis, N.
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- 2011
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14. Multiple Small Bowel Diverticula Were an Unexpected Finding During Laparoscopic Enterectomy for Crohn's Disease
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Sotirova, I. Gklavas, A. Papalouka, D. Gourtsoyianni, S. Christodoulou, D. Papaconstantinou, I.
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Introduction: Small bowel diverticulosis (SBD) is a rare entity. Although it is usually an asymptomatic condition, clinical manifestations may vary from non-specific clinical signs to severe and complicated disease. The coexistence of SBD and Crohn's disease (CD) is rarely reported in the current literature. Aim: We present a rare case of concomitant Crohn's disease (CD) and SBD in a male patient, where multiple jejunal diverticula were an incidental intraoperative finding. Preoperative evaluation with magnetic resonance enterography (MRE) failed to recognize the coexistence of these two entities. Surgeons should be aware of the possibility of this rare situation. Case report: A 52-year-old Caucasian male diagnosed with CD was referred to our department for surgical intervention due to an ileal stricture. The patient reported no past medical history, except for a few episodes of bloody diarrhoea during a three-year period. The index colonoscopy revealed luminal narrowing in the ileum at approximately 70 cm proximal to the ileocaecal valve, and biopsies revealed findings compatible with CD. Clinical examination and laboratory tests were unremarkable one day before surgery. The patient underwent laparoscopic segmental resection of the affected part of the ileum. Intraoperatively, multiple non-inflamed diverticula along the jejunum extending from the Treitz ligament to the proximal ileum were recognized. Our patient had an uncomplicated post-operative course and was discharged on the fifth post-operative day. Pathological examination revealed features compatible with CD in the active phase. The patient was referred to his gastroenterological team for further consultation regarding the appropriate post-operative management. Conclusion: Concomitant CD and SBD is a rare condition, and the differential diagnosis may be challenging due to overlapping symptoms. © 2020 Ira Sotirova, Antonios Gklavas, Dimitra Papalouka, Sofia Gourtsoyianni, Dimitrios Christodoulou, Ioannis Papaconstantinou.
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- 2020
15. Apparent diffusion coefficient measurements on a novel diffusion weighted MRI phantom utilizing EPI and HASTE sequences
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Kalaitzakis, G. Boursianis, T. Gourzoulidis, G. Gourtsoyianni, S. Lymperopoulou, G. Marias, K. Karantanas, A. Maris, T.G.
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body regions - Abstract
Purpose: The aim of this study is to introduce a novel DWI-MRI phantom and to compare Apparent Diffusion Coefficient (ADC) measurements, utilizing EPI-DWI and HASTE-DWI sequences and two different fitting algorithms. Materials and Methods: 23 test tubes with different sucrose concentrations and polyacrylamide gels were used as a phantom for ADC measurements. The phantom was scanned on a clinical MRI system (1.5 T) over a two-month period utilizing an EPI-DWI and a HASTE-DWI sequence. ADC maps were calculated using a Weighted Linear (WL) and a Non Linear (NL) fitting algorithm. Measurements were performed with two sequences and two fitting algorithms. Geometric Distortions (GD), Ghosting Ratios (GR) and Signal to Structured Noise Ratios (SSNRs) were estimated using both sequences from the resultant ADC parametric maps. Results: Polyacrylamide gels reveal lower coefficient of variation (CV%) as compared to sucrose solutions. ADC measurements performed with WL and NL algorithms reveal identical results with both sequences. WL and NL algorithms require approx. 3 s and 7 min respectively, for a single slice. EPI-DWI reveals a mean percent ADC value difference of (+4.5%) as compared to HASTE-DWI, regardless the type of fitting algorithm. Conclusion: Polyacrylamide gels can serve as a better means for simulating ADC values, compared with sucrose solutions used in this study. WL can be proposed as the method for ADC measurements in daily clinical practice. WL is significantly faster than NL fitting method and equally precise. SSNR measured directly on ADC maps is an excellent means for testing the precision of ADC measurements. © 2020 Associazione Italiana di Fisica Medica
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- 2020
16. Vergleich von 2D- und 3D-Sequenzen für die MRCP: Klinischer Stellenwert der einzelnen Techniken
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Wallnoefer, A. M., Herrmann, K. A., Beuers, U., Zech, C. J., Gourtsoyianni, S., Reiser, M. F., and Schoenberg, S. O.
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- 2005
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17. Patient deprivation and perceived scan burden negatively impact the quality of whole-body MRI
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Evans, R.E.C., primary, Taylor, S.A., additional, Kalasthry, J., additional, Sakai, N.S., additional, Miles, A., additional, Aboagye, A., additional, Agoramoorthy, L., additional, Ahmed, S., additional, Amadi, A., additional, Anand, G., additional, Atkin, G., additional, Austria, A., additional, Ball, S., additional, Bazari, F., additional, Beable, R., additional, Beare, S., additional, Beedham, H., additional, Beeston, T., additional, Bharwani, N., additional, Bhatnagar, G., additional, Bhowmik, A., additional, Blakeway, L., additional, Blunt, D., additional, Boavida, P., additional, Boisfer, D., additional, Breen, D., additional, Bridgewater, J., additional, Burke, S., additional, Butawan, R., additional, Campbell, Y., additional, Chang, E., additional, Chao, D., additional, Chukundah, S., additional, Clarke, C.S., additional, Collins, B., additional, Collins, C., additional, Conteh, V., additional, Couture, J., additional, Crosbie, J., additional, Curtis, H., additional, Daniel, A., additional, Davis, L., additional, Desai, K., additional, Duggan, M., additional, Ellis, S., additional, Elton, C., additional, Engledow, A., additional, Everitt, C., additional, Ferdous, S., additional, Frow, A., additional, Furneaux, M., additional, Gibbons, N., additional, Glynne-Jones, R., additional, Gogbashian, A., additional, Goh, V., additional, Gourtsoyianni, S., additional, Green, A., additional, Green, Laura, additional, Green, Liz, additional, Groves, A., additional, Guthrie, A., additional, Hadley, E., additional, Halligan, S., additional, Hameeduddin, A., additional, Hanid, G., additional, Hans, S., additional, Hans, B., additional, Higginson, A., additional, Honeyfield, L., additional, Hughes, H., additional, Hughes, J., additional, Hurl, L., additional, Isaac, E., additional, Jackson, M., additional, Jalloh, A., additional, Janes, S., additional, Jannapureddy, R., additional, Jayme, A., additional, Johnson, A., additional, Johnson, E., additional, Julka, P., additional, Karapanagiotou, E., additional, Karp, S., additional, Kay, C., additional, Kellaway, J., additional, Khan, S., additional, Koh, D., additional, Light, T., additional, Limbu, P., additional, Lock, S., additional, Locke, I., additional, Loke, T., additional, Lowe, A., additional, Lucas, N., additional, Maheswaran, S., additional, Mallett, S., additional, Marwood, E., additional, McGowan, J., additional, Mckirdy, F., additional, Mills-Baldock, T., additional, Moon, T., additional, Morgan, V., additional, Morris, S., additional, Morton, A., additional, Nasseri, S., additional, Navani, N., additional, Nichols, P., additional, Norman, C., additional, Ntala, E., additional, Nunes, A., additional, Obichere, A., additional, O'Donohue, J., additional, Olaleye, I., additional, Oliver, A., additional, Onajobi, A., additional, O'Shaughnessy, T., additional, Padhani, A., additional, Pardoe, H., additional, Partridge, W., additional, Patel, U., additional, Perry, K., additional, Piga, W., additional, Prezzi, D., additional, Prior, K., additional, Punwani, S., additional, Pyers, J., additional, Rafiee, H., additional, Rahman, F., additional, Rajanpandian, I., additional, Ramesh, S., additional, Raouf, S., additional, Reczko, K., additional, Reinhardt, A., additional, Robinson, D., additional, Rockall, A., additional, Russell, P., additional, Sargus, K., additional, Scurr, E., additional, Shahabuddin, K., additional, Sharp, A., additional, Shepherd, B., additional, Shiu, K., additional, Sidhu, H., additional, Simcock, I., additional, Simeon, C., additional, Smith, A., additional, Smith, D., additional, Snell, D., additional, Spence, J., additional, Srirajaskanthan, R., additional, Stachini, V., additional, Stegner, S., additional, Stirling, J., additional, Strickland, N., additional, Tarver, K., additional, Teague, J., additional, Thaha, M., additional, Train, M., additional, Tulmuntaha, S., additional, Tunariu, N., additional, van Ree, K., additional, Verjee, A., additional, Wanstall, C., additional, Weir, S., additional, Wijeyekoon, S., additional, Wilson, J., additional, Wilson, S., additional, Win, T., additional, Woodrow, L., additional, and Yu, D., additional
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- 2020
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18. Patient preferences for whole-body MRI or conventional staging pathways in lung and colorectal cancer: a discrete choice experiment
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Miles, A, Taylor, SA, Evans, REC, Halligan, S, Beare, S, Bridgewater, J, Goh, V, Janes, S, Navani, N, Oliver, A, Morton, A, Rockall, A, Clarke, CS, Morris, S, Aboagye, A, Agoramoorthy, L, Ahmed, S, Amadi, A, Anand, G, Atkin, G, Austria, A, Ball, S, Bazari, F, Beable, R, Beedham, H, Beeston, T, Bharwani, N, Bhatnagar, G, Bhowmik, A, Blakeway, L, Blunt, D, Boavida, P, Boisfer, D, Breen, D, Burke, S, Butawan, R, Campbell, Y, Chang, E, Chao, D, Chukundah, S, Collins, B, Collins, C, Conteh, V, Couture, J, Crosbie, J, Curtis, H, Daniel, A, Davis, L, Desai, K, Duggan, M, Ellis, S, Elton, C, Engledow, A, Everitt, C, Ferdous, S, Frow, A, Furneaux, M, Gibbons, N, Glynne-Jones, R, Gogbashian, A, Gourtsoyianni, S, Green, A, Green, L, Groves, A, Guthrie, A, Hadley, E, Hameeduddin, A, Hanid, G, Hans, S, Hans, B, Higginson, A, Honeyfield, L, Hughes, H, Hughes, J, Hurl, L, Isaac, E, Jackson, M, Jalloh, A, Jannapureddy, R, Jayme, A, Johnson, A, Johnson, E, Julka, P, Kalasthry, J, Karapanagiotou, E, Karp, S, Kay, C, Kellaway, J, Khan, S, Koh, D-M, Light, T, Limbu, P, Lock, S, Locke, I, Loke, T, Lowe, A, Lucas, N, Maheswaran, S, Mallett, S, Marwood, E, McGowan, J, Mckirdy, F, Mills-Baldock, T, Moon, T, Morgan, V, Nasseri, S, Nichols, P, Norman, C, Ntala, E, Nunes, A, Obichere, A, O'Donohue, J, Olaleye, I, Onajobi, A, O'Shaughnessy, T, Padhani, A, Pardoe, H, Partridge, W, Patel, U, Perry, K, Piga, W, Prezzi, D, Prior, K, Punwani, S, Pyers, J, Rafiee, H, Rahman, F, Rajanpandian, I, Ramesh, S, Raouf, S, Reczko, K, Reinhardt, A, Robinson, D, Russell, P, Sargus, K, Scurr, E, Shahabuddin, K, Sharp, A, Shepherd, B, Shiu, K, Sidhu, H, Simcock, I, Simeon, C, Smith, A, Smith, D, Snell, D, Spence, J, Srirajaskanthan, R, Stachini, V, Stegner, S, Stirling, J, Strickland, N, Tarver, K, Teague, J, Thaha, M, Train, M, Tulmuntaha, S, Tunariu, N, Van Ree, K, Verjee, A, Wanstall, C, Weir, S, Wijeyekoon, S, Wilson, J, Wilson, S, Win, T, Woodrow, L, Yu, D, Imperial College Healthcare NHS Trust- BRC Funding, and Department of Health
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Adult ,Male ,Positron emission tomography ,Lung Neoplasms ,Social Sciences ,X-ray computed ,Magnetic resonance imaging ,Psychology, Multidisciplinary ,Positron Emission Tomography Computed Tomography ,Surveys and Questionnaires ,Psychology ,Humans ,Whole Body Imaging ,Patient preference ,Prospective Studies ,Tomography ,Cancer ,Aged ,Neoplasm Staging ,Science & Technology ,Radiology, Nuclear Medicine & Medical Imaging ,Tomography, X-ray computed ,1103 Clinical Sciences ,CARE ,Middle Aged ,NEGATIVE AFFECT ,Biomedical Social Sciences ,Social Sciences, Biomedical ,Nuclear Medicine & Medical Imaging ,PANAS ,Oncology ,Positron-Emission Tomography ,Regression Analysis ,CLAUSTROPHOBIA ,Female ,STREAMLINE investigators ,Colorectal Neoplasms ,Life Sciences & Biomedicine - Abstract
Objectives To determine the importance placed by patients on attributes associated with whole-body MRI (WB-MRI) and standard cancer staging pathways and ascertain drivers of preference. Methods Patients recruited to two multi-centre diagnostic accuracy trials comparing WB-MRI with standard staging pathways in lung and colorectal cancer were invited to complete a discrete choice experiment (DCE), choosing between a series of alternate pathways in which 6 attributes (accuracy, time to diagnosis, scan duration, whole-body enclosure, radiation exposure, total scan number) were varied systematically. Data were analysed using a conditional logit regression model and marginal rates of substitution computed. The relative importance of each attribute and probabilities of choosing WB-MRI-based pathways were estimated. Results A total of 138 patients (mean age 65, 61% male, lung n = 72, colorectal n = 66) participated (May 2015 to September 2016). Lung cancer patients valued time to diagnosis most highly, followed by accuracy, radiation exposure, number of scans, and time in the scanner. Colorectal cancer patients valued accuracy most highly, followed by time to diagnosis, radiation exposure, and number of scans. Patients were willing to wait 0.29 (lung) and 0.45 (colorectal) weeks for a 1% increase in pathway accuracy. Patients preferred WB-MRI-based pathways (probability 0.64 [lung], 0.66 [colorectal]) if they were equivalent in accuracy, total scan number, and time to diagnosis compared with a standard staging pathway. Conclusions Staging pathways based on first-line WB-MRI are preferred by the majority of patients if they at least match standard pathways for diagnostic accuracy, time to diagnosis, and total scan number.
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- 2019
19. Proceedings of the International Cancer Imaging Society (ICIS) 16th Annual Teaching Course
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Koh, Dow-Mu, Kaste, Sue Creviston, Vinnicombe, Sarah J., Morana, Giovanni, Rossi, Andrea, Herold, Christian J., McLoud, Theresa C., Frey, Kirk A., Gebauer, Bernhard, Roebuck, Derek, Fütterer, Jurgen J., Towbin, Alexander J., Huisman, Thierry A. G., Smets, Anne M. J. B., Lee, Jeong Min, Chandarana, Hersh, Mayerhoefer, Marius E., Raderer, Markus, Haug, Alexander, Eiber, Matthias, Rockall, Andrea, Sohaib, Aslam, Warbey, Victoria S, Vargas, Hebert Alberto, Heiken, Jay P., Francis, Isaac R., Al-Hawary, Mahmoud M., Kaza, Ravi K., D’Onofrio, Mirko, Thoeny, Harriet C., King, Ann D., Piccardo, Arnoldo, Garrè, Maria Luisa, Reed, Nick, Rodriguez-Galindo, Carlos, Wasnik, Ashish P., Diederich, Stefan, Oyen, Wim J. G., Chaw, Cheng Lee, van As, Nicholas, Vieira, Igor, De Keyzer, Frederik, Dresen, Elleke, Han, Sileny, Vergote, Ignace, Moerman, Philippe, Amant, Frederic, Koole, Michel, Vandecaveye, Vincent, Dresen, R., De Vuysere, S., De Keyzer, F., Van Cutsem, E., D’Hoore, A., Wolthuis, A., Vandecaveye, V., Pricolo, P., Alessi, S., Summers, P., Tagliabue, E., Petralia, G., Pfannenberg, C., Gückel, B., Schüle, S. C., Müller, A. C., Kaufmann, S., Schwenzer, N., Reimold, M., la Fougere, C., Nikolaou, K., Martus, P., Cook, G. J., Azad, G. K., Taylor, B. P., Siddique, M., John, J., Mansi, J., Harries, M., Goh, V., Seth, S., Burgul, R., Seth, A., Waugh, S., Gowdh, N. Muhammad, Purdie, C., Evans, A., Crowe, E., Thompson, A., Vinnicombe, S., Arfeen, F., Campion, T., Goldstraw, E., D’Onofrio, M., Ciaravino, V., Crosara, S., De Robertis, R., Mucelli, R. Pozzi, Uhrig, M., Simons, D., Schlemmer, H., Downey, Kate, Murdoch, S., Al-adhami, A. S., Viswanathan, S., Smith, S., Jennings, P., Bowers, D., Soomal, R., Mutala, T. M., Odhiambo, A. O., Harish, N., Hall, M., Sproule, M., Sheridan, S., Thein, K. Y., Tan, C. H., Thian, Y. L., Ho, C. M., De Luca, S., Carrera, C., Blanchet, V., Alarcón, L., Eyheremnedy, E., Choudhury, B. K., Bujarbarua, K., Barman, G., Lovat, E., Ferner, R., Warbey, V. S., Potti, L., Kaye, B., Beattie, A., Dutton, K., Seth, A. A., Constantinidis, F., Dobson, H., Bradley, R., Bozas, G., Avery, G., Stephens, A., Maraveyas, A., Bhuva, S., Johnson, C. A., Subesinghe, M., Taylor, N., Quint, L. E., Reddy, R. M., Kalemkerian, G. P., Zapico, G. González, Jauregui, E. Gainza, Francisco, R. Álvarez, Alonso, S. Ibáñez, Bahillo, I. Tavera, Álvarez, L. Múgica, Francies, O., Wheeler, R., Childs, L., Adams, A., Sahdev, A., De Luca, S. E., Vañek, M. E. Casalini, Pascuzzi, M. D., Gillanders, T., Ramos, P. M., Eyheremendy, E. P., Stove, C., Digby, M., Nazar, M., Wirtz, M., Troncoso, F., Saguier, F., Quint, D. J., Dang, L., Carlson, M., Leber, S., Silverstein, F., Rueben, R., Nazir, B., Teo, T. H., Khoo, J. B., Sharma, K., Gupta, N., Mathew, B., Jeyakumar, T., Harkins, K., Joshua, S., Christodoulou, D., Gourtsoyianni, S., Jacques, A., Griffin, N., Lee, J., Goodfellow, J. A., Yong, A., Jenkins, S., Joseph, G., Partington, K., Zanfardini, A., Cavanagh, K., and Lau, E.
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lcsh:Medical physics. Medical radiology. Nuclear medicine ,Radiological and Ultrasound Technology ,Oncology ,Radiology Nuclear Medicine and imaging ,lcsh:R895-920 ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Meeting Abstracts ,lcsh:RC254-282 - Abstract
Table of contents O1 Tumour heterogeneity: what does it mean? Dow-Mu Koh O2 Skeletal sequelae in adult survivors of childhood cancer Sue Creviston Kaste O3 Locoregional effects of breast cancer treatment Sarah J Vinnicombe O4 Imaging of cancer therapy-induced CNS toxicity Giovanni Morana, Andrea Rossi O5 Screening for lung cancer Christian J. Herold O6Risk stratification of lung nodules Theresa C. McLoud O7 PET imaging of pulmonary nodules Kirk A Frey O8 Transarterial tumour therapy Bernhard Gebauer O9 Interventional radiology in paediatric oncology Derek Roebuck O10 Image guided prostate interventions Jurgen J. Fütterer O11 Imaging cancer predisposition syndromes Alexander J. Towbin O12Chest and chest wall masses Thierry AG Huisman O13 Abdominal masses: good or bad? Anne MJB Smets O14 Hepatobiliary MR contrast: enhanced liver MRI for HCC diagnosis and management Giovanni Morana O15 Role of US elastography and multimodality fusion for managing patients with chronic liver disease and HCC Jeong Min Lee O16 Opportunities and challenges in imaging metastatic disease Hersh Chandarana O17 Diagnosis, treatment monitoring, and follow-up of lymphoma Marius E. Mayerhoefer, Markus Raderer, Alexander Haug O18 Managing high-risk and advanced prostate cancer Matthias Eiber O19 Immunotherapy: imaging challenges Bernhard Gebauer O20 RECIST and RECIST 1.1 Andrea Rockall O21 Challenges of RECIST in oncology imaging basics for the trainee and novice Aslam Sohaib O22 Lymphoma: PET for interim and end of treatment response assessment: a users’ guide to the Deauville Score Victoria S Warbey O23 Available resources Hebert Alberto Vargas O24 ICIS e-portal and the online learning community Dow-Mu Koh O25 Benign lesions that mimic pancreatic cancer Jay P Heiken O26 Staging and reporting pancreatic malignancies Isaac R Francis, Mahmoud, M Al-Hawary, Ravi K Kaza O27 Intraductal papillary mucinous neoplasm Giovanni Morana O28 Cystic pancreatic tumours Mirko D’Onofrio O29 Diffusion-weighted imaging of head and neck tumours Harriet C. Thoeny O30 Radiation injury in the head and neck Ann D King O31 PET/MR of paediatric brain tumours Giovanni Morana, Arnoldo Piccardo, Maria Luisa Garrè, Andrea Rossi O32 Structured reporting and beyond Hebert Alberto Vargas O33 Massachusetts General Hospital experience with structured reporting Theresa C. McLoud O34 The oncologist’s perspective: what the oncologist needs to know Nick Reed O35 Towards the cure of all children with cancer: global initiatives in pediatric oncology Carlos Rodriguez-Galindo O36 Multiparametric imaging of renal cancers Hersh Chandarana O37 Linking imaging features of renal disease and their impact on management strategies Hebert Alberto Vargas O38 Adrenals, retroperitoneum and peritoneum Isaac R Francis, Ashish P Wasnik O39 Lung and pleura Stefan Diederich O40 Advances in MRI Jurgen J. Fütterer O41 Advances in molecular imaging Wim J.G. Oyen O42 Incorporating advanced imaging, impact on treatment selection and patient outcome Cheng Lee Chaw, Nicholas van As S1 Combining ADC-histogram features improves performance of MR diffusion-weighted imaging for Lymph node characterisation in cervical cancer Igor Vieira, Frederik De Keyzer, Elleke Dresen, Sileny Han, Ignace Vergote, Philippe Moerman, Frederic Amant, Michel Koole, Vincent Vandecaveye S2 Whole-body diffusion-weighted MRI for surgical planning in patients with colorectal cancer and peritoneal metastases R Dresen, S De Vuysere, F De Keyzer, E Van Cutsem, A D’Hoore, A Wolthuis, V Vandecaveye S3 Role of apparent diffusion coefficient (ADC) diffusion-weighted MRI for predicting extra capsular extension of prostate cancer. P. Pricolo (paola.pricolo@ieo.it), S. Alessi, P. Summers, E. Tagliabue, G. Petralia S4 Generating evidence for clinical benefit of PET/CT – are management studies sufficient as surrogate for patient outcome? C. Pfannenberg, B. Gückel, SC Schüle, AC Müller, S. Kaufmann, N. Schwenzer, M. Reimold,C. la Fougere, K. Nikolaou, P. Martus S5 Heterogeneity of treatment response in skeletal metastases from breast cancer with 18F-fluoride and 18F-FDG PET GJ Cook, GK Azad, BP Taylor, M Siddique, J John, J Mansi, M Harries, V Goh S6 Accuracy of suspicious breast imaging—can we tell the patient? S Seth, R Burgul, A Seth S7 Measurement method of tumour volume changes during neoadjuvant chemotherapy affects ability to predict pathological response S Waugh, N Muhammad Gowdh, C Purdie, A Evans, E Crowe, A Thompson, S Vinnicombe S8 Diagnostic yield of CT IVU in haematuria screening F. Arfeen, T. Campion, E. Goldstraw S9 Percutaneous radiofrequency ablation of unresectable locally advanced pancreatic cancer: preliminary results D’Onofrio M, Ciaravino V, Crosara S, De Robertis R, Pozzi Mucelli R S10 Iodine maps from dual energy CT improve detection of metastases in staging examinations of melanoma patients M. Uhrig, D. Simons, H. Schlemmer S11Can contrast enhanced CT predict pelvic nodal status in malignant melanoma of the lower limb? Kate Downey S12 Current practice in the investigation for suspected Paraneoplastic Neurological Syndromes (PNS) and positive malignancy yield. S Murdoch, AS Al-adhami, S Viswanathan P1 Technical success and efficacy of Pulmonary Radiofrequency ablation: an analysis of 207 ablations S Smith, P Jennings, D Bowers, R Soomal P2 Lesion control and patient outcome: prospective analysis of radiofrequency abaltion in pulmonary colorectal cancer metastatic disease S Smith, P Jennings, D Bowers, R Soomal P3 Hepatocellular carcinoma in a post-TB patient: case of tropical infections and oncologic imaging challenges TM Mutala, AO Odhiambo, N Harish P4 Role of apparent diffusion coefficient (ADC) diffusion-weighted MRI for predicting extracapsular extension of prostate cancer P. Pricolo, S. Alessi, P. Summers, E. Tagliabue, G. Petralia P5 What a difference a decade makes; comparison of lung biopsies in Glasgow 2005 and 2015 M. Hall, M. Sproule, S. Sheridan P6 Solid pseudopapillary tumour of pancreas: imaging features of a rare neoplasm KY Thein, CH Tan, YL Thian, CM Ho P7 MDCT - pathological correlation in colon adenocarcinoma staging: preliminary experience S De Luca, C Carrera, V Blanchet, L Alarcón, E Eyheremnedy P8 Image guided biopsy of thoracic masses and reduction of pneumothorax risk: 25 years experience B K Choudhury, K Bujarbarua, G Barman P9 Tumour heterogeneity analysis of 18F-FDG-PET for characterisation of malignant peripheral nerve sheath tumours in neurofibromatosis-1 GJ Cook, E Lovat, M Siddique, V Goh, R Ferner, VS Warbey P10 Impact of introduction of vacuum assisted excision (VAE) on screen detected high risk breast lesions L Potti, B Kaye, A Beattie, K Dutton P11 Can we reduce prevalent recall rate in breast screening? AA Seth, F Constantinidis, H Dobson P12 How to reduce prevalent recall rate? Identifying mammographic lesions with low Positive Predictive Value (PPV) AA Seth (archana.seth@nhs.net), F Constantinidis, H Dobson P13 Behaviour of untreated pulmonary thrombus in oncology patients diagnosed with incidental pulmonary embolism on CT R. Bradley, G. Bozas, G. Avery, A. Stephens, A. Maraveyas P14 A one-stop lymphoma biopsy service – is it possible? S Bhuva, CA Johnson, M Subesinghe, N Taylor P15 Changes in the new TNM classification for lung cancer (8th edition, effective January 2017) LE Quint, RM Reddy, GP Kalemkerian P16 Cancer immunotherapy: a review of adequate imaging assessment G González Zapico, E Gainza Jauregui, R Álvarez Francisco, S Ibáñez Alonso, I Tavera Bahillo, L Múgica Álvarez P17 Succinate dehydrogenase mutations and their associated tumours O Francies, R Wheeler, L Childs, A Adams, A Sahdev P18 Initial experience in the usefulness of dual energy technique in the abdomen SE De Luca, ME Casalini Vañek, MD Pascuzzi, T Gillanders, PM Ramos, EP Eyheremendy P19 Recognising the serious complication of Richter’s transformation in CLL patients C Stove, M Digby P20 Body diffusion-weighted MRI in oncologic practice: truths, tricks and tips M. Nazar, M. Wirtz, MD. Pascuzzi, F. Troncoso, F. Saguier, EP. Eyheremendy P21 Methotrexate-induced leukoencephalopathy in paediatric ALL Patients D.J. Quint, L. Dang, M. Carlson, S. Leber, F. Silverstein P22 Pitfalls in oncology CT reporting. A pictorial review R Rueben, S Viswanathan P23 Imaging of perineural extension in head and neck tumours B Nazir, TH Teo, JB Khoo P24 MRI findings of molecular subtypes of breast cancer: a pictorial primer K Sharma, N Gupta, B Mathew, T Jeyakumar, K Harkins P25 When cancer can’t wait! A pictorial review of oncological emergencies K Sharma, B Mathew, N Gupta, T Jeyakumar, S Joshua P26 MRI of pancreatic neuroendocrine tumours: an approach to interpretation D Christodoulou, S Gourtsoyianni, A Jacques, N Griffin, V Goh P27 Gynaecological cancers in pregnancy: a review of imaging CA Johnson, J Lee P28 Suspected paraneoplastic neurological syndromes - review of published recommendations to date, with proposed guideline/flowchart JA Goodfellow, AS Al-adhami, S Viswanathan P29 Multi-parametric MRI of the pelvis for suspected local recurrence of prostate cancer after radical prostatectomy R Bradley P30 Utilisation of PI-RADS version 2 in multi-parametric MRI of the prostate; 12-months experience R Bradley P31 Radiological assessment of the post-chemotherapy liver A Yong, S Jenkins, G Joseph P32 Skeletal staging with MRI in breast cancer – what the radiologist needs to know S Bhuva, K Partington P33 Perineural spread of lympoma: an educational review of an unusual distribution of disease CA Johnson, S Bhuva, M Subesinghe, N Taylor P34 Visually isoattenuating pancreatic adenocarcinoma. Diagnostic imaging tools. C Carrera, A Zanfardini, S De Luca, L Alarcón, V Blanchet, EP Eyheremendy P35 Imaging of larynx cancer: when is CT, MRI or FDG PET/CT the best test? K Cavanagh, E Lau
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- 2016
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20. Magnetic resonance imaging for clinical management of rectal cancer: Updated recommendations from the 2016 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus meeting
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Beets-Tan, RGH, Lambregts, DMJ, Maas, M, Bipat, S, Barbaro, B, Curvo-Semedo, L, Fenlon, HM, Gollub, MJ, Gourtsoyianni, S, Halligan, S, Hoeffel, C, Kim, SH, Laghi, A, Maier, A, Rafaelsen, SR, Stoker, J, Taylor, SA, Torkzad, MR, Blomqvist, L, Beets-Tan, RGH, Lambregts, DMJ, Maas, M, Bipat, S, Barbaro, B, Curvo-Semedo, L, Fenlon, HM, Gollub, MJ, Gourtsoyianni, S, Halligan, S, Hoeffel, C, Kim, SH, Laghi, A, Maier, A, Rafaelsen, SR, Stoker, J, Taylor, SA, Torkzad, MR, and Blomqvist, L
- Abstract
OBJECTIVES: To update the 2012 ESGAR consensus guidelines on the acquisition, interpretation and reporting of magnetic resonance imaging (MRI) for clinical staging and restaging of rectal cancer. METHODS: Fourteen abdominal imaging experts from the European Society of Gastrointestinal and Abdominal Radiology (ESGAR) participated in a consensus meeting, organised according to an adaptation of the RAND-UCLA Appropriateness Method. Two independent (non-voting) Chairs facilitated the meeting. 246 items were scored (comprising 229 items from the previous 2012 consensus and 17 additional items) and classified as 'appropriate' or 'inappropriate' (defined by ≥ 80 % consensus) or uncertain (defined by < 80 % consensus). RESULTS: Consensus was reached for 226 (92 %) of items. From these recommendations regarding hardware, patient preparation, imaging sequences and acquisition, criteria for MR imaging evaluation and reporting structure were constructed. The main additions to the 2012 consensus include recommendations regarding use of diffusion-weighted imaging, criteria for nodal staging and a recommended structured report template. CONCLUSIONS: These updated expert consensus recommendations should be used as clinical guidelines for primary staging and restaging of rectal cancer using MRI. KEY POINTS: • These guidelines present recommendations for staging and reporting of rectal cancer. • The guidelines were constructed through consensus amongst 14 pelvic imaging experts. • Consensus was reached by the experts for 92 % of the 246 items discussed. • Practical guidelines for nodal staging are proposed. • A structured reporting template is presented.
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- 2018
21. Magnetic resonance imaging for clinical management of rectal cancer: Updated recommendations from the 2016 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus meeting
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Beets-Tan, R. G. H., Lambregts, D. M. J., Maas, M., Bipat, S., Barbaro, Brunella, Curvo-Semedo, L., Fenlon, H. M., Gollub, M. J., Gourtsoyianni, S., Halligan, S., Hoeffel, C., Kim, S. H., Laghi, A., Maier, A., Rafaelsen, S. R., Stoker, J., Taylor, S. A., Torkzad, M. R., Blomqvist, L., Barbaro B. (ORCID:0000-0002-9638-543X), Beets-Tan, R. G. H., Lambregts, D. M. J., Maas, M., Bipat, S., Barbaro, Brunella, Curvo-Semedo, L., Fenlon, H. M., Gollub, M. J., Gourtsoyianni, S., Halligan, S., Hoeffel, C., Kim, S. H., Laghi, A., Maier, A., Rafaelsen, S. R., Stoker, J., Taylor, S. A., Torkzad, M. R., Blomqvist, L., and Barbaro B. (ORCID:0000-0002-9638-543X)
- Abstract
Objectives: To update the 2012 ESGAR consensus guidelines on the acquisition, interpretation and reporting of magnetic resonance imaging (MRI) for clinical staging and restaging of rectal cancer. Methods: Fourteen abdominal imaging experts from the European Society of Gastrointestinal and Abdominal Radiology (ESGAR) participated in a consensus meeting, organised according to an adaptation of the RAND-UCLA Appropriateness Method. Two independent (non-voting) Chairs facilitated the meeting. 246 items were scored (comprising 229 items from the previous 2012 consensus and 17 additional items) and classified as ‘appropriate’ or ‘inappropriate’ (defined by ≥ 80 % consensus) or uncertain (defined by OpenSPiltSPi 80 % consensus). Results: Consensus was reached for 226 (92 %) of items. From these recommendations regarding hardware, patient preparation, imaging sequences and acquisition, criteria for MR imaging evaluation and reporting structure were constructed. The main additions to the 2012 consensus include recommendations regarding use of diffusion-weighted imaging, criteria for nodal staging and a recommended structured report template. Conclusions: These updated expert consensus recommendations should be used as clinical guidelines for primary staging and restaging of rectal cancer using MRI. Key Points: • These guidelines present recommendations for staging and reporting of rectal cancer. • The guidelines were constructed through consensus amongst 14 pelvic imaging experts. • Consensus was reached by the experts for 92 % of the 246 items discussed. • Practical guidelines for nodal staging are proposed. • A structured reporting template is presented.
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- 2018
22. MRI at the completion of chemoradiotherapy can accurately evaluate the extent of disease in women with advanced urethral carcinoma undergoing anterior pelvic exenteration
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Gourtsoyianni S, Hudolin T, Sala E, Goldman D, Bochner BH, Hricak H.
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Vulvar cancer, MRI, anterior pelvic exenteration - Abstract
In women with advanced primary urethral cancer, MRI is an excellent tool for monitoring neo-adjuvant chemoradiotherapy changes and evaluating the extent of disease before exenterative surgery.
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- 2011
23. Split-Bolus CT for Patients with abdominal Pain
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Zamboni, Giulia, Gourtsoyianni, S, Romero, Jy, and Raptopoulos, Vd
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Nontraumatic Abdominal Emergencies ,CT imaging ,Emergency - Published
- 2010
24. Split iv-bolus technique in abdominal CT of emergency room patients with acute abdominal pain
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Zamboni, Giulia, Gourtsoyianni, S, Romero, J, and Raptopoulos, V.
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techniques ,abdominal CT ,acute abdominen - Published
- 2008
25. Routine Use of CT Enterography in Patients with Acute Abdominal Pain
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Gourtsoyianni, S, Zamboni, Giulia, Romero, J, and Raptopoulos, V.
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CT Enterography ,Abdomen - Published
- 2007
26. Impact of z-axis dose modulation on CT exam image quality and choice of mA
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Zamboni, Giulia, Brennan, Dd, Gourtsoyianni, S, Kataoka, Ml, Kruskal, Jb, and Raptopoulos, V.
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CT ,Imaging techniques - Published
- 2006
27. Magnetic resonance imaging for the clinical management of rectal cancer patients: recommendations from the 2012 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus meeting.
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Beets Tan, Rg, Lambregts, Dm, Maas, M, Bipat, S, Barbaro, Brunella, Caseiro Alves, F, Curvo Semedo, L, Fenlon, Hm, Gollub, Mj, Gourtsoyianni, S, Halligan, S, Hoeffel, C, Kim, Sh, Laghi, A, Maier, A, Rafaelsen, Sr, Stoker, J, Taylor, Sa, Torkzad, Mr, Blomqvist, L., Barbaro, Brunella (ORCID:0000-0002-9638-543X), Beets Tan, Rg, Lambregts, Dm, Maas, M, Bipat, S, Barbaro, Brunella, Caseiro Alves, F, Curvo Semedo, L, Fenlon, Hm, Gollub, Mj, Gourtsoyianni, S, Halligan, S, Hoeffel, C, Kim, Sh, Laghi, A, Maier, A, Rafaelsen, Sr, Stoker, J, Taylor, Sa, Torkzad, Mr, Blomqvist, L., and Barbaro, Brunella (ORCID:0000-0002-9638-543X)
- Abstract
OBJECTIVES: To develop guidelines describing a standardised approach regarding the acquisition, interpretation and reporting of magnetic resonance imaging (MRI) for clinical staging and restaging of rectal cancer. METHODS: A consensus meeting of 14 abdominal imaging experts from the European Society of Gastrointestinal and Abdominal Radiology (ESGAR) was conducted following the RAND-UCLA Appropriateness Method. Two independent (non-voting) chairs facilitated the meeting. Two hundred and thirty-six items were scored by participants for appropriateness and classified subsequently as appropriate or inappropriate (defined by ≥ 80 % consensus) or uncertain (defined by < 80 % consensus). Items not reaching 80 % consensus were noted. RESULTS: Consensus was reached for 88 % of items: recommendations regarding hardware, patient preparation, imaging sequences, angulation, criteria for MRI assessment and MRI reporting were constructed from these. CONCLUSIONS: These expert consensus recommendations can be used as clinical guidelines for primary staging and restaging of rectal cancer using MRI.
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- 2013
28. MRI of anal cancer: assessing response to definitive chemoradiotherapy
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Gourtsoyianni, S., primary and Goh, V., additional
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- 2013
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29. Reproducibility and clinical correlations of post-treatment changes on CT of prostate cancer bone metastases treated with chemotherapy
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Gourtsoyianni, S, primary, Hwang, S, additional, Panicek, D M, additional, Zheng, J, additional, Moskowitz, C, additional, Scher, H, additional, Morris, M, additional, and Hricak, H, additional
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- 2012
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30. Standardisation of liver MDCT by tracking liver parenchyma enhancement to trigger imaging
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Brodoefel, H., primary, Tognolini, A., additional, Zamboni, G. A., additional, Gourtsoyianni, S., additional, Claussen, C. D., additional, and Raptopoulos, V., additional
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- 2011
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31. Evaluation of a patient-specific Monte Carlo software for CT dosimetry
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Myronakis, M., primary, Perisinakis, K., additional, Tzedakis, A., additional, Gourtsoyianni, S., additional, and Damilakis, J., additional
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- 2009
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32. Differenzialdiagnose unklarer neurologischer Störungen bei immunsupprimierten Patienten unter Cyclosporin-Therapie
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Gourtsoyianni, S, primary, Michaely, HJ, additional, Wagner, S, additional, Schoenberg, S, additional, and Reiser, M, additional
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- 2005
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33. Twenty years on: RECIST as a biomarker of response in solid tumours. An EORTC Imaging Group – ESOI joint paper
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Fournier, L, de Geus-Oei, L-F, Regge, D, Oprea-Lager, D E, Danastasi, M, Bidaut, Luc, Baeuerle, T, Lopci, E, Cappello, G, Lecouvet, F, Mayerhoefer, M E, Kunz, W G, Verhoeff, J, Caruso, D, Smits, M, Hoffmann, R-T, Gourtsoyianni, S, Beets-Tan, R G H, Neri, E, de Souza, N, Deroose, C M, Caramella, C, Fournier, L, de Geus-Oei, L-F, Regge, D, Oprea-Lager, D E, Danastasi, M, Bidaut, Luc, Baeuerle, T, Lopci, E, Cappello, G, Lecouvet, F, Mayerhoefer, M E, Kunz, W G, Verhoeff, J, Caruso, D, Smits, M, Hoffmann, R-T, Gourtsoyianni, S, Beets-Tan, R G H, Neri, E, de Souza, N, Deroose, C M, and Caramella, C
- Abstract
Response evaluation criteria in solid tumours (RECIST) v1.1 are currently the reference standard for evaluating efficacy of therapies in patients with solid tumours who are included in clinical trials, and they are widely used and accepted by regulatory agencies. This expert statement discusses the principles underlying RECIST, as well as their reproducibility and limitations. While the RECIST framework may not be perfect, the scientific bases for the anticancer drugs that have been approved using a RECIST-based surrogate endpoint remain valid. Importantly, changes in measurement have to meet thresholds defined by RECIST for reponse classification within thus partly circumventing the problems of measurement variability. The RECIST framework also applies to clinical patients in individual settings even though the relationship between tumour size changes and outcome from cohort studies is not necessarily translatable to individual cases. As reproducibility of RECIST measurements is impacted by reader experience, choice of target lesions and detection/interpretation of new lesions, it can result in patients changing response categories when measurements are near threshold values or if new lesions are missed or incorrectly interpreted. There are several situations where RECIST will fail to evaluate treatment-induced changes correctly; knowledge and understanding of these is crucial for correct interpretation. Also, some patterns of response/progression cannot be correctly documented by RECIST, particularly in relation to organ-site (e.g. bone without associated soft-tissue lesion) and treatment type (e.g. focal therapies). These require specialist reader experience and communication with oncologists to determine the actual impact of the therapy and best evaluation strategy. In such situations, alternative imaging markers for tumour response may be used but the sources of variability of individual imaging techniques need to be known and accounted for. Communication betwe
34. Imaging standardisation in metastatic colorectal cancer: a joint EORTC-ESOI-ESGAR expert consensus recommendation
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Unterrainer, Marcus, Deroose, Christophe M., Herrmann, Ken, Moehler, Markus, Blomqvist, Lennart, Cannella, Roberto, Caramella, Caroline, Caruso, Damiano, Chouhan, Manil D., Denecke, Timm, De la Pinta, Carolina, De Geus-Oei, Lioe-Fee, Dulskas, Audrius, Eisenblätter, Michel, Foley, Kieran G., Gourtsoyianni, Sofia, Lecouvet, Frederic E., Lopci, Egesta, Maas, Monique, Obmann, Markus M., Oprea-Lager, Daniela E., Verhoeff, Joost J. C., Santiago, Ines, Terraz, Sylvain, D'Anastasi, Melvin, Regge, Daniele, Laghi, Andrea, Beets-Tan, Regina G. H., Heinemann, Volker, Lordick, Florian, Smyth, Elizabeth C., Ricke, Jens, Kunz, Wolfgang G., European Organisation for Research and Treatment of Cancer (EORTC), Imaging Group, the European Organisation for Research and Treatment of Cancer (EORTC), Gastrointestinal Tract Cancer Group, the European Society of Oncologic Imaging (ESOI), European Society of Gastrointestinal and Abdominal Radiology (ESGAR)., Radiology and nuclear medicine, CCA - Imaging and biomarkers, Unterrainer M., Deroose C.M., Herrmann K., Moehler M., Blomqvist L., Cannella R., Caramella C., Caruso D., Chouhan M.D., Denecke T., De la Pinta C., De Geus-Oei L.F., Dulskas A., Eisenblätter M., Foley K.G., Gourtsoyianni S., Lecouvet F.E., Lopci E., Maas M., Obmann M.M., Oprea-Lager D.E., Verhoeff J.J.C., Santiago I., Terraz S., D'Anastasi M., Regge D., Laghi A., Beets-Tan R.G.H., Heinemann V., Lordick F., Smyth E.C., Ricke J., Kunz W.G., European Organisation for Research and Treatment of Cancer (EORTC), Imaging Group, the European Organisation for Research and Treatment of Cancer (EORTC), Gastrointestinal Tract Cancer Group, the European Society of Oncologic Imaging (ESOI), and European Society of Gastrointestinal and Abdominal Radiology (ESGAR).
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PROTOCOL ,Cancer Research ,Positron emission tomography ,Artificial intelligence ,Consensus ,BEVACIZUMAB ,Medizin ,Imaging ,Cancer -- Imaging ,Humans ,CRITERIA ,Colon (Anatomy) -- Cancer -- Tomography ,Computed tomography ,Science & Technology ,Radiomics ,Rectal Neoplasms ,Abdomen -- Radiography -- Case studies ,Colon (Anatomy) -- Cancer -- Treatment ,Reproducibility of Results ,Abdomen -- Radiography -- Standards ,OPEN-LABEL ,Colorectal cancer ,Artificial intelligence, Standardisation, Colorectal cancer, Computed tomography, Imaging, Positron emission tomography, Radiomics ,Oncology ,Colonic Neoplasms ,SURVIVAL ,Standardisation ,Life Sciences & Biomedicine - Abstract
Background: Treatment monitoring in metastatic colorectal cancer (mCRC) relies on imaging to evaluate the tumor burden. Response Evaluation Criteria in Solid Tumors (RECIST) provide a framework on reporting and interpretation of imaging findings yet offer no guidance on a standardized imaging protocol tailored to mCRC patients. Imaging protocol heterogeneity remains a challenge for the reproducibility of conventional imaging endpoints and is an obstacle for research on novel imaging endpoints. Patients and methods: Acknowledging the recently highlighted potential of radiomics and artificial intelligence (AI) tools as decision support for patient care in mCRC, a multidisciplinary, international, and expert panel of imaging specialists was formed to find consensus on mCRC imaging protocols using the Delphi method. Results: Under the guidance of the European Organisation for Research and Treatment of Cancer (EORTC) Imaging and Gastrointestinal Tract Cancer Groups, the European Society of Oncologic Imaging (ESOI) and the European Society of Gastrointestinal and Abdominal Radiology (ESGAR), the EORTC-ESOI-ESGAR core imaging protocol was identified. Conclusion: This consensus protocol attempts to promote standardization and to diminish variations in patient preparation, scan acquisition and scan reconstruction. We anticipate that this standardization will increase reproducibility of radiomics and AI studies and serve as a catalyst for future research on imaging endpoints. For ongoing and future mCRC trials, we encourage principal investigators to support the dissemination of these imaging standards across recruiting centers., peer-reviewed
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- 2022
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35. Multivariable prognostic modelling to improve prediction of colorectal cancer recurrence: the PROSPeCT trial.
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Goh V, Mallett S, Boulter V, Glynne-Jones R, Khan S, Lessels S, Patel D, Prezzi D, Rodriguez-Justo M, Taylor SA, Beable R, Betts M, Breen DJ, Britton I, Brush J, Correa P, Dodds N, Dunlop J, Gourtsoyianni S, Griffin N, Higginson A, Lowe A, Slater A, Strugnell M, Tolan D, Zealley I, and Halligan S
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- Humans, Male, Female, Aged, Prognosis, Prospective Studies, Middle Aged, Biomarkers, Tumor, Neoplasm Staging, Sensitivity and Specificity, Immunohistochemistry, Colorectal Neoplasms pathology, Colorectal Neoplasms diagnostic imaging, Neoplasm Recurrence, Local diagnostic imaging, Tomography, X-Ray Computed methods
- Abstract
Objective: Improving prognostication to direct personalised therapy remains an unmet need. This study prospectively investigated promising CT, genetic, and immunohistochemical markers to improve the prediction of colorectal cancer recurrence., Material and Methods: This multicentre trial (ISRCTN 95037515) recruited patients with primary colorectal cancer undergoing CT staging from 13 hospitals. Follow-up identified cancer recurrence and death. A baseline model for cancer recurrence at 3 years was developed from pre-specified clinicopathological variables (age, sex, tumour-node stage, tumour size, location, extramural venous invasion, and treatment). Then, CT perfusion (blood flow, blood volume, transit time and permeability), genetic (RAS, RAF, and DNA mismatch repair), and immunohistochemical markers of angiogenesis and hypoxia (CD105, vascular endothelial growth factor, glucose transporter protein, and hypoxia-inducible factor) were added to assess whether prediction improved over tumour-node staging alone as the main outcome measure., Results: Three hundred twenty-six of 448 participants formed the final cohort (226 male; mean 66 ± 10 years. 227 (70%) had ≥ T3 stage cancers; 151 (46%) were node-positive; 81 (25%) developed subsequent recurrence. The sensitivity and specificity of staging alone for recurrence were 0.56 [95% CI: 0.44, 0.67] and 0.58 [0.51, 0.64], respectively. The baseline clinicopathologic model improved specificity (0.74 [0.68, 0.79], with equivalent sensitivity of 0.57 [0.45, 0.68] for high vs medium/low-risk participants. The addition of prespecified CT perfusion, genetic, and immunohistochemical markers did not improve prediction over and above the clinicopathologic model (sensitivity, 0.58-0.68; specificity, 0.75-0.76)., Conclusion: A multivariable clinicopathological model outperformed staging in identifying patients at high risk of recurrence. Promising CT, genetic, and immunohistochemical markers investigated did not further improve prognostication in rigorous prospective evaluation., Clinical Relevance Statement: A prognostic model based on clinicopathological variables including age, sex, tumour-node stage, size, location, and extramural venous invasion better identifies colorectal cancer patients at high risk of recurrence for neoadjuvant/adjuvant therapy than stage alone., Key Points: Identification of colorectal cancer patients at high risk of recurrence is an unmet need for treatment personalisation. This model for recurrence, incorporating many patient variables, had higher specificity than staging alone. Continued optimisation of risk stratification schema will help individualise treatment plans and follow-up schedules., (© 2024. The Author(s).)
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- 2024
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36. ESR Essentials: response assessment criteria in oncologic imaging-practice recommendations by the European Society of Oncologic Imaging.
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Zamboni GA, Cappello G, Caruso D, Gourtsoyianni S, Cyran C, Schlemmer HP, D'Anastasi M, Fournier L, and Neri E
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Assessing the response to oncological treatments is paramount for determining the prognosis and defining the best treatment for each patient. Several biomarkers, including imaging, can be used, but standardization is fundamental for consistency and reliability. Tumor response evaluation criteria have been defined by international groups for application in pharmaceutical clinical trials evaluating new drugs or therapeutic strategies. RECIST 1.1 criteria are exclusively based on unidimensional lesion measurements; changes in tumor size are used as surrogate imaging biomarkers to correlate with patient outcomes. However, increased tumor size does not always reflect tumor progression. The introduction of immunotherapy has led to the development of new criteria (iRECIST, Level of Evidence (LoE) Ib) that consider the possibility that an increase in disease burden is secondary to the immune response instead of progression, with the new concept of Unconfirmed Progressive Disease (a first progression event which must be confirmed on follow-up). Specific criteria were devised for HCC (mRECIST, LoE IV), which measure only enhancing HCC portions to account for changes after local therapy. For GIST treated with imatinib, criteria were developed to account for the possible increase in size reflecting a response rather than a progression by assessing both tumor size and density on CT (Choi, LoE II). This article provides concise and relevant practice recommendations aimed at general radiologists to help choose and apply the most appropriate criteria for assessing response to treatment in different oncologic scenarios. Though these criteria were developed for clinical trials, they may be applied in clinical practice as a guide for day-to-day interpretation. KEY POINTS: Response evaluation criteria, designed for use in clinical trials, might serve as a surrogate biomarker for overall survival. RECIST 1.1 defines measurable and non-measurable disease among which target lesions and non-target lesions are selected at baseline as reference for follow-ups. Some therapies and/or cancers require the use of different criteria, such as iRECIST, mRECIST, and Choi criteria., (© 2024. The Author(s).)
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- 2024
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37. An Automated Prognostic Model for Pancreatic Ductal Adenocarcinoma.
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Vezakis I, Vezakis A, Gourtsoyianni S, Koutoulidis V, Polydorou AA, Matsopoulos GK, and Koutsouris DD
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- Humans, Prognosis, Pancreas, Pancreatic Neoplasms, Pancreatic Neoplasms diagnostic imaging, Carcinoma, Pancreatic Ductal diagnostic imaging
- Abstract
Pancreatic ductal adenocarcinoma (PDAC) constitutes a leading cause of cancer-related mortality despite advances in detection and treatment methods. While computed tomography (CT) serves as the current gold standard for initial evaluation of PDAC, its prognostic value remains limited, as it relies on diagnostic stage parameters encompassing tumor size, lymph node involvement, and metastasis. Radiomics have recently shown promise in predicting postoperative survival of PDAC patients; however, they rely on manual pancreas and tumor delineation by clinicians. In this study, we collected a dataset of pre-operative CT scans from a cohort of 40 PDAC patients to evaluate a fully automated pipeline for survival prediction. Employing nnU-Net trained on an external dataset, we generated automated pancreas and tumor segmentations. Subsequently, we extracted 854 radiomic features from each segmentation, which we narrowed down to 29 via feature selection. We then combined these features with the Tumor, Node, Metastasis (TNM) system staging parameters, as well as the patient's age. We trained a random survival forest model to perform an overall survival prediction over time, as well as a random forest classifier for the binary classification of two-year survival, using repeated cross-validation for evaluation. Our results exhibited promise, with a mean C-index of 0.731 for survival modeling and a mean accuracy of 0.76 in two-year survival prediction, providing evidence of the feasibility and potential efficacy of a fully automated pipeline for PDAC prognostication. By eliminating the labor-intensive manual segmentation process, our streamlined pipeline demonstrates an efficient and accurate prognostication process, laying the foundation for future research endeavors.
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- 2023
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38. The Spectrum of Solitary Benign Splenic Lesions-Imaging Clues for a Noninvasive Diagnosis.
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Gourtsoyianni S, Laniado M, Ros-Mendoza L, Mansueto G, and Zamboni GA
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Cross-sectional imaging of the upper abdomen, especially if intravenous contrast has been administered, will most likely reveal any acute or chronic disease harbored in the spleen. Unless imaging is performed with the specific purpose of evaluating the spleen or characterizing a known splenic lesion, incidentally discovered splenic lesions pose a small challenge. Solitary benign splenic lesions include cysts, hemangiomas, sclerosing angiomatous nodular transformation (SANT), hamartomas, and abscesses, among others. Sarcoidosis and tuberculosis, although predominantly diffuse micronodular disease processes, may also present as a solitary splenic mass lesion. In addition, infarction and rupture, both traumatic and spontaneous, may take place in the spleen. This review aims to describe the imaging features of the most common benign focal splenic lesions, with emphasis on the imaging findings as these are encountered on routine cross-sectional imaging from a multicenter pool of cases that, coupled with clinical information, can allow a definite diagnosis.
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- 2023
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39. Intraductal Papillary Mucinous Neoplasm of the Pancreas: A Challenging Diagnosis.
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Triantopoulou C, Gourtsoyianni S, Karakaxas D, and Delis S
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Intraductal papillary mucinous neoplasm of the pancreas (IPMN) was classified as a distinct entity from mucinous cystic neoplasm by the WHO in 1995. It represents a mucin-producing tumor that originates from the ductal epithelium and can evolve from slight dysplasia to invasive carcinoma. In addition, different aspects of tumor progression may be seen in the same lesion. Three types are recognized, the branch duct variant, the main duct variant, which shows a much higher prevalence for malignancy, and the mixed-type variant, which combines branch and main duct characteristics. Advances in cross-sectional imaging have led to an increased rate of IPMN detection. The main imaging characteristic of IPMN is the dilatation of the pancreatic duct without the presence of an obstructing lesion. The diagnosis of a branch duct IPMN is based on the proof of its communication with the main pancreatic duct on MRI-MRCP examination. Early identification by imaging of the so-called worrisome features or predictors for malignancy is an important and challenging task. In this review, we will present recent imaging advances in the diagnosis and characterization of different types of IPMNs, as well as imaging tools available for early recognition of worrisome features for malignancy. A critical appraisal of current IPMN management guidelines from both a radiologist's and surgeon's perspective will be made. Special mention is made of complications that might arise during the course of IPMNs as well as concomitant pancreatic neoplasms including pancreatic adenocarcinoma and pancreatic endocrine neoplasms. Finally, recent research on prognostic and predictive biomarkers including radiomics will be discussed.
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- 2023
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40. Attitudes and perceptions of radiologists towards online (virtual) oncologic multidisciplinary team meetings during the COVID-19 pandemic-a survey of the European Society of Oncologic Imaging (ESOI).
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Bonanno N, Cioni D, Caruso D, Cyran CC, Dinkel J, Fournier L, Gourtsoyianni S, Hoffmann RT, Laghi A, Martincich L, Mayerhoefer ME, Zamboni GA, Sala E, Schlemmer HP, Neri E, and D'Anastasi M
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- Humans, Pandemics, Radiologists, Surveys and Questionnaires, Patient Care Team, COVID-19
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Objectives: To explore radiologists' opinions regarding the shift from in-person oncologic multidisciplinary team meetings (MDTMs) to online MDTMs. To assess the perceived impact of online MDTMs, and to evaluate clinical and technical aspects of online meetings., Methods: An online questionnaire including 24 questions was e-mailed to all European Society of Oncologic Imaging (ESOI) members. Questions targeted the structure and efficacy of online MDTMs, including benefits and limitations., Results: A total of 204 radiologists responded to the survey. Responses were evaluated using descriptive statistical analysis. The majority (157/204; 77%) reported a shift to online MDTMs at the start of the pandemic. For the most part, this transition had a positive effect on maintaining and improving attendance. The majority of participants reported that online MDTMs provide the same clinical standard as in-person meetings, and that interdisciplinary discussion and review of imaging data were not hindered. Seventy three of 204 (35.8%) participants favour reverting to in-person MDTs, once safe to do so, while 7/204 (3.4%) prefer a continuation of online MDTMs. The majority (124/204, 60.8%) prefer a combination of physical and online MDTMs., Conclusions: Online MDTMs are a viable alternative to in-person meetings enabling continued timely high-quality provision of care with maintained coordination between specialties. They were accepted by the majority of surveyed radiologists who also favoured their continuation after the pandemic, preferably in combination with in-person meetings. An awareness of communication issues particular to online meetings is important. Training, improved software, and availability of support are essential to overcome technical and IT difficulties reported by participants., Key Points: • Majority of surveyed radiologists reported shift from in-person to online oncologic MDT meetings during the COVID-19 pandemic. • The shift to online MDTMs was feasible and generally accepted by the radiologists surveyed with the majority reporting that online MDTMs provide the same clinical standard as in-person meetings. • Most would favour the return to in-person MDTMs but would also accept the continued use of online MDTMs following the end of the current pandemic., (© 2022. The Author(s), under exclusive licence to European Society of Radiology.)
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- 2023
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41. Comparison between 1.5-T and 3.0-T MRI for the diagnosis of placenta accreta spectrum disorders.
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Bourgioti C, Zafeiropoulou K, Tzavara C, Daskalakis G, Fotopoulos S, Theodora M, Nikolaidou ME, Konidari M, Gourtsoyianni S, Panourgias E, Koutoulidis V, Martzoukos EA, Konstantinidou AE, and Moulopoulos LA
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- Adult, Female, Gestational Age, Humans, Infant, Magnetic Resonance Imaging methods, Male, Placenta, Pregnancy, Prenatal Diagnosis methods, Retrospective Studies, Placenta Accreta diagnostic imaging
- Abstract
Purpose: Accurate antenatal diagnosis of placenta accreta spectrum (PAS) is important for optimal management. The purpose of this study was to compare the respective capabilities of 1.5-T and 3.0-T MRI in the diagnosis of PAS., Materials and Methods: Between March 2016-March 2021, 190 pregnant women at high risk for PAS underwent dedicated prenatal MRI with either 1.5-T or 3.0-T units at a tertiary imaging center. Cesarian section and MRI were performed less than 6 weeks from each other. Prospectively collected data were evaluated by two experienced genitourinary radiologists for presence and extent of PAS. A comparative study was designed to investigate differences in predictive ability between 1.5-T and 3.0-T MRI groups. Sensitivity, specificity, accuracy, negative and positive prognostic values relative to intraoperative/histological findings, were computed for both groups and were compared with chi-square (χ 2) test. Interobserver agreement was estimated using Kappa test., Results: One hundred-eighty-two gravid women were included in the study; of these, 91/182 (50%) women were evaluated with 1.5-T (mean age, 35 ± 5.1 [SD] years; mean gestational age: 32.5 weeks) and 91/182 (50%) with 3.0-T MRI (mean age, 34.9 ± 4.9 [SD] years; mean gestational age, 32.1 weeks). 1.5-T MRI yielded 95.7% sensitivity (95% CI: 87.8-99.1) and 81.8% specificity (95% CI: 59.8) and 3.0-T MRI 93.8% sensitivity (95% CI: 86.0-97.9) and 83.3% specificity (95% CI: 48.2-97.7) for PAS identification, with no differences between the two groups (P = 0.725 and P >0.999, respectively). MRI showed excellent predictive ability for detecting extrauterine placental spread with 100% sensitivity (95% CI: 89.4-100.0), 96.7% specificity (95% CI: 88.1-99.6) for 1.5-T and 97% sensitivity (95% CI: 84.2-99.9), 96.7% specificity (95% CI: 88.1-99.6) for 3.0-T without differences between the two groups (P > 0.999). Interobserver agreement was excellent for both groups. The most frequently detected MRI signs of PAS for both 1.5-T and 3.0-T groups were placental heterogeneity (n = 85, 93.5% vs. n = 90, 98.9%; P = 0.413), and intraplacental fetal vessels (n = 64, 70.3% vs. n = 65, 71.4%; P = 0.870)., Conclusion: This study suggests that 3.0-T MRI and 1.5-T MRI are equivalent for the diagnosis of PAS., Competing Interests: Disclosure of interest The authors declare that they have no known competing financial or personal relationships that could be viewed as influencing the work reported in this paper., (Copyright © 2022 Société française de radiologie. Published by Elsevier Masson SAS. All rights reserved.)
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- 2022
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42. Twenty Years On: RECIST as a Biomarker of Response in Solid Tumours an EORTC Imaging Group - ESOI Joint Paper.
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Fournier L, de Geus-Oei LF, Regge D, Oprea-Lager DE, D'Anastasi M, Bidaut L, Bäuerle T, Lopci E, Cappello G, Lecouvet F, Mayerhoefer M, Kunz WG, Verhoeff JJC, Caruso D, Smits M, Hoffmann RT, Gourtsoyianni S, Beets-Tan R, Neri E, deSouza NM, Deroose CM, and Caramella C
- Abstract
Response evaluation criteria in solid tumours (RECIST) v1.1 are currently the reference standard for evaluating efficacy of therapies in patients with solid tumours who are included in clinical trials, and they are widely used and accepted by regulatory agencies. This expert statement discusses the principles underlying RECIST, as well as their reproducibility and limitations. While the RECIST framework may not be perfect, the scientific bases for the anticancer drugs that have been approved using a RECIST-based surrogate endpoint remain valid. Importantly, changes in measurement have to meet thresholds defined by RECIST for response classification within thus partly circumventing the problems of measurement variability. The RECIST framework also applies to clinical patients in individual settings even though the relationship between tumour size changes and outcome from cohort studies is not necessarily translatable to individual cases. As reproducibility of RECIST measurements is impacted by reader experience, choice of target lesions and detection/interpretation of new lesions, it can result in patients changing response categories when measurements are near threshold values or if new lesions are missed or incorrectly interpreted. There are several situations where RECIST will fail to evaluate treatment-induced changes correctly; knowledge and understanding of these is crucial for correct interpretation. Also, some patterns of response/progression cannot be correctly documented by RECIST, particularly in relation to organ-site (e.g. bone without associated soft-tissue lesion) and treatment type (e.g. focal therapies). These require specialist reader experience and communication with oncologists to determine the actual impact of the therapy and best evaluation strategy. In such situations, alternative imaging markers for tumour response may be used but the sources of variability of individual imaging techniques need to be known and accounted for. Communication between imaging experts and oncologists regarding the level of confidence in a biomarker is essential for the correct interpretation of a biomarker and its application to clinical decision-making. Though measurement automation is desirable and potentially reduces the variability of results, associated technical difficulties must be overcome, and human adjudications may be required., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Fournier, de Geus-Oei, Regge, Oprea-Lager, D’Anastasi, Bidaut, Bäuerle, Lopci, Cappello, Lecouvet, Mayerhoefer, Kunz, Verhoeff, Caruso, Smits, Hoffmann, Gourtsoyianni, Beets-Tan, Neri, deSouza, Deroose and Caramella.)
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- 2022
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43. Imaging during pregnancy: What the radiologist needs to know.
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Bourgioti C, Konidari M, Gourtsoyianni S, and Moulopoulos LA
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- Diagnostic Imaging, Female, Fetus diagnostic imaging, Humans, Pregnancy, Radiologists, Diagnostic Tests, Routine, Pregnancy Complications diagnostic imaging
- Abstract
During the last decades, there has been a growing demand for medical imaging in gravid women. Imaging of the pregnant woman is challenging as it involves both the mother and the fetus and, consequently, several medical, ethical, or legal considerations are likely to be raised. Theoretically, all currently available imaging modalities may be used for the evaluation of the pregnant woman; however, in practice, confusion regarding the safety of the fetus often results in unnecessary avoidance of useful diagnostic tests, especially those involving ionizing radiation. This review article is focused on the current safety guidelines and considerations regarding the use of different imaging modalities in the pregnant population; also presented is an imaging work-up for the most common medical conditions of pregnant women, with emphasis on fetal and maternal safety., (Copyright © 2021 Société française de radiologie. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2021
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44. Management of the adenocarcinoma of the upper rectum: a reappraisal.
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Pechlivanides G, Gourtsoyianni S, Gouvas N, Sougklakos J, and Xynos E
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- Chemoradiotherapy, Adjuvant, Chemotherapy, Adjuvant, Humans, Neoadjuvant Therapy, Neoplasm Staging, Rectum pathology, Rectum surgery, Treatment Outcome, Adenocarcinoma pathology, Rectal Neoplasms pathology
- Abstract
The present review attempts to assess whether upper rectal cancer (URC) should be treated either as colon cancer or as rectal one, namely to be managed with upfront surgery without neo-adjuvant treatment and partial mesorectal excision (PME), or with neo-adjuvant short course radiotherapy (SCRT) or chemoradiotherapy (CRT) as indicated, followed by surgery with total mesorectal excision. Reports from current evidence including studies, reviews and various guidelines are conflicting. Main reasons for inability to reach safe conclusions are (i) the various anatomical definitions of the rectum and its upper part, (ii) the inadequate preoperative local staging,(iii) the heterogeneity of selection criteria for the neo-adjuvant treatment,(iv) the different neo-adjuvant treatment regimens, and(v) the variety in the extent of surgical resection, among the studies. Although not adequately supported, locally advanced URC can be treated with neo-adjuvant CRT provided the lesion is within the radiation field of safety, and a PME if the lower border of the tumour is located above the anterior peritoneal reflection. There is evidence that adjuvant chemotherapy is of benefit in high-risk stage II and stage III lesions.
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- 2021
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45. Hellenic society of medical oncology (HESMO) guidelines for the management of anal cancer.
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Gouvas N, Gourtsoyianni S, Kalogeridi MA, Sougklakos J, Vini L, and Xynos E
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- Algorithms, Anus Neoplasms etiology, Carcinoma, Squamous Cell etiology, Cyprus, Delivery of Health Care, Europe, Female, Greece, Humans, Male, Papillomavirus Infections complications, Anus Neoplasms diagnosis, Anus Neoplasms therapy, Carcinoma, Squamous Cell diagnosis, Carcinoma, Squamous Cell therapy, Consensus, Interdisciplinary Communication, Medical Oncology organization & administration, Patient Care Team, Practice Guidelines as Topic, Societies, Medical organization & administration
- Abstract
Despite considerable improvement in the management of anal cancer, there is a great deal of variation in the outcomes among European countries, and in particular among different hospital centres in Greece and Cyprus. The aim was to elaborate a consensus on the multidisciplinary management of anal cancer, based on European guidelines (European Society of Medical Oncologists-ESMO), considering local special characteristics of our healthcare system. Following discussion and online communication among members of an executive team, a consensus was developed. Guidelines are proposed along with algorithms of diagnosis and treatment. The importance of centralisation, care by a multidisciplinary team (MDT) and adherence to guidelines are emphasised.
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- 2021
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46. Involvement of radiologists in oncologic multidisciplinary team meetings: an international survey by the European Society of Oncologic Imaging.
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Neri E, Gabelloni M, Bäuerle T, Beets-Tan R, Caruso D, D'Anastasi M, Dinkel J, Fournier LS, Gourtsoyianni S, Hoffmann RT, Mayerhöfer ME, Regge D, Schlemmer HP, and Laghi A
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- Humans, Patient Care Team, Radiologists, Surveys and Questionnaires, Medical Oncology, Neoplasms diagnostic imaging, Neoplasms therapy
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Objectives: Multidisciplinary tumour boards (MTBs) play an increasingly important role in managing cancer patients from diagnosis to treatment. However, many problems arise around the organisation of MTBs, both in terms of organisation-administration and time management. In this context, the European Society of Oncologic Imaging (ESOI) conducted a survey among its members, aimed at assessing the quality and amount of involvement of radiologists in MTBs, their role in it and related issues., Methods: All members were invited to fill in a questionnaire consisting of 15 questions with both open and multiple-choice answers. Simple descriptive analyses and graphs were performed., Results: A total of 292 ESOI members in full standing for the year 2018 joined the survey. Most respondents (89%) declared to attend MT-Bs, but only 114 respondents (43.9%) review over 70% of exams prior to MTB meetings, mainly due to lack of time due to a busy schedule for imaging and reporting (46.6%). Perceived benefits (i.e. surgical and histological feedback (86.9%), improved knowledge of cancer treatment (82.7%) and better interaction between radiologists and referring clinicians for discussing rare cases (56.9%)) and issues (i.e. attending MTB meetings during regular working hours (71.9%) and lack of accreditation with continuing medical education (CME) (85%)) are reported., Conclusions: Despite the value and benefits of radiologists' participation in MTBs, issues like improper preparation due to a busy schedule and no counterpart in CME accreditation require efforts to improve the role of radiologists for a better patient care., Key Points: • Most radiologists attend multidisciplinary tumour boards, but less than half of them review images in advance, mostly due to time constraints. • Feedback about radiological diagnoses, improved knowledge of cancer treatment and interaction with referring clinicians are perceived as major benefits. • Concerns were expressed about scheduling multidisciplinary tumour boards during regular working hours and lack of accreditation with continuing medical education.
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- 2021
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47. Diffusion-weighted imaging and texture analysis: current role for diffuse liver disease.
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Gourtsoyianni S, Santinha J, Matos C, and Papanikolaou N
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- Humans, Magnetic Resonance Imaging, Diffusion Magnetic Resonance Imaging, Liver Diseases diagnostic imaging
- Abstract
Multiparametric MRI represents the primary imaging modality to assess diffuse liver disease, both in a qualitative and in a quantitative manner. Diffusion-weighted imaging (DWI) is among the imaging techniques that can be used to assess fibrosis due to its unique capability to assess microstructural changes at the tissue level. DWI is based on water mobility patterns and has the potential to become a non-invasive and non-destructive virtual biopsy to assess diffuse liver disease, overcoming sampling bias errors due to its three-dimensional imaging capabilities. Parallel to DWI, another quantitative method called texture analysis may be used to assess early and advanced diffused liver disease through quantifying spatial relationships in a global and local level, applying to any type of digital imaging technique like MRI or CT. Initial results using texture analysis hold great promise. In the current paper, we will review the role of DWI and texture analysis using MR images in assessing diffuse liver disease.
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- 2020
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48. Apparent diffusion coefficient measurements on a novel diffusion weighted MRI phantom utilizing EPI and HASTE sequences.
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Kalaitzakis G, Boursianis T, Gourzoulidis G, Gourtsoyianni S, Lymperopoulou G, Marias K, Karantanas A, and Maris TG
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- Linear Models, Diffusion Magnetic Resonance Imaging instrumentation, Phantoms, Imaging
- Abstract
Purpose: The aim of this study is to introduce a novel DWI-MRI phantom and to compare Apparent Diffusion Coefficient (ADC) measurements, utilizing EPI-DWI and HASTE-DWI sequences and two different fitting algorithms., Materials and Methods: 23 test tubes with different sucrose concentrations and polyacrylamide gels were used as a phantom for ADC measurements. The phantom was scanned on a clinical MRI system (1.5 T) over a two-month period utilizing an EPI-DWI and a HASTE-DWI sequence. ADC maps were calculated using a Weighted Linear (WL) and a Non Linear (NL) fitting algorithm. Measurements were performed with two sequences and two fitting algorithms. Geometric Distortions (GD), Ghosting Ratios (GR) and Signal to Structured Noise Ratios (SSNRs) were estimated using both sequences from the resultant ADC parametric maps., Results: Polyacrylamide gels reveal lower coefficient of variation (CV%) as compared to sucrose solutions. ADC measurements performed with WL and NL algorithms reveal identical results with both sequences. WL and NL algorithms require approx. 3 s and 7 min respectively, for a single slice. EPI-DWI reveals a mean percent ADC value difference of (+4.5%) as compared to HASTE-DWI, regardless the type of fitting algorithm., Conclusion: Polyacrylamide gels can serve as a better means for simulating ADC values, compared with sucrose solutions used in this study. WL can be proposed as the method for ADC measurements in daily clinical practice. WL is significantly faster than NL fitting method and equally precise. SSNR measured directly on ADC maps is an excellent means for testing the precision of ADC measurements., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Associazione Italiana di Fisica Medica. Published by Elsevier Ltd. All rights reserved.)
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- 2020
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49. Multiple Small Bowel Diverticula Were an Unexpected Finding During Laparoscopic Enterectomy for Crohn's Disease.
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Sotirova I, Gklavas A, Papalouka D, Gourtsoyianni S, Christodoulou D, and Papaconstantinou I
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- Constriction, Pathologic, Crohn Disease complications, Crohn Disease diagnostic imaging, Diverticulum complications, Humans, Ileal Diseases complications, Ileal Diseases diagnostic imaging, Jejunal Diseases complications, Laparoscopy, Magnetic Resonance Imaging, Male, Middle Aged, Crohn Disease surgery, Diverticulum diagnosis, Ileal Diseases surgery, Incidental Findings, Intestine, Small abnormalities, Jejunal Diseases diagnosis
- Abstract
Introduction: Small bowel diverticulosis (SBD) is a rare entity. Although it is usually an asymptomatic condition, clinical manifestations may vary from non-specific clinical signs to severe and complicated disease. The coexistence of SBD and Crohn's disease (CD) is rarely reported in the current literature., Aim: We present a rare case of concomitant Crohn's disease (CD) and SBD in a male patient, where multiple jejunal diverticula were an incidental intraoperative finding. Preoperative evaluation with magnetic resonance enterography (MRE) failed to recognize the coexistence of these two entities. Surgeons should be aware of the possibility of this rare situation., Case Report: A 52-year-old Caucasian male diagnosed with CD was referred to our department for surgical intervention due to an ileal stricture. The patient reported no past medical history, except for a few episodes of bloody diarrhoea during a three-year period. The index colonoscopy revealed luminal narrowing in the ileum at approximately 70 cm proximal to the ileocaecal valve, and biopsies revealed findings compatible with CD. Clinical examination and laboratory tests were unremarkable one day before surgery. The patient underwent laparoscopic segmental resection of the affected part of the ileum. Intraoperatively, multiple non-inflamed diverticula along the jejunum extending from the Treitz ligament to the proximal ileum were recognized. Our patient had an uncomplicated post-operative course and was discharged on the fifth post-operative day. Pathological examination revealed features compatible with CD in the active phase. The patient was referred to his gastroenterological team for further consultation regarding the appropriate post-operative management., Conclusion: Concomitant CD and SBD is a rare condition, and the differential diagnosis may be challenging due to overlapping symptoms., Competing Interests: The authors declare that they have no conflict of interest., (© 2020 Ira Sotirova, Antonios Gklavas, Dimitra Papalouka, Sofia Gourtsoyianni, Dimitrios Christodoulou, Ioannis Papaconstantinou.)
- Published
- 2020
- Full Text
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50. Consensus statement of the Hellenic and Cypriot Gastric Cancer Study Group on the diagnosis, staging and management of gastric cancer.
- Author
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Douridas GN, Fountoulakis A, Souglakos J, Gourtsoyianni S, Vini L, Levidou G, Liakakos T, Agalianos C, Dervenis C, Kalogeridi MA, Karavokyros I, Koumarianou A, Kountourakis P, Oikonomopoulos G, Economopoulou P, Sgouros J, Sgouros SN, Stamou K, Triantopoulou C, Zacharoulis D, Gouvas N, and Xynos E
- Subjects
- Humans, Neoplasm Staging, Stomach Neoplasms pathology, Consensus, Stomach Neoplasms diagnosis, Stomach Neoplasms therapy
- Abstract
Gastric Cancer epidemics have changed over recent decades, declining in incidence, shifting from distal to proximal location, transforming from intestinal to diffuse histology. Novel chemotherapeutic agents combined with modern surgical operations hardly changed overall disease related survival. This may be attributed to a substantial inherent geographical variation of disease genetics, but also to a failure to standardize and implement treatment protocols in clinical practice. To overcome these drawbacks in Greece and Cyprus, a Gastric Cancer Study Group under the auspices of the Hellenic Society of Medical Oncology (HeSMO) and Gastrointestinal Cancer Study Group (GIC-SG) merged their efforts to produce a consensus considering ethnic parameters of healthcare system and the international proposals as well. Utilizing structured meetings of experts, a consensus was reached. To achieve further consensus, statements were subjected to the Delphi methodology by invited multidisciplinary national and international experts. Sentences were considered of high or low consensus if they were voted by ≥ 80%, or < 80%, respectively; those obtaining a low consensus level after both voting rounds were rejected. Forty-five statements were developed and voted by 71 experts. The median rate of abstention per statement was 9.9% (range: 0-53.5%). At the end of the process, one statement was rejected, another revised, and all the remaining achieved a high consensus. Forty-four recommendations covering all aspects of the management of gastric cancer and concise treatment algorithms are proposed by the Hellenic and Cypriot Gastric Cancer Study Group. The importance of centralization, care by a multidisciplinary team, adherence to guidelines, and individualization are emphasized.
- Published
- 2020
- Full Text
- View/download PDF
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