38 results on '"Jurgenliemk-Schulz, I."'
Search Results
2. MO-0050 Feasibility of the determination of the molecular-integrated risk profile in the PORTEC-4a trial
- Author
-
van den Heerik, A., primary, Horeweg, N., additional, Lutgens, L., additional, Haverkort, D., additional, Kommoss, S., additional, Staebler, A., additional, Koppe, F., additional, Nowee, M., additional, Westerveld, H., additional, de Jong, M., additional, Cibula, D., additional, Dundr, P., additional, Cnossen, J., additional, Mens, J.W., additional, Chargari, C., additional, Genestie, C., additional, Bijmolt, S., additional, Gillham, C., additional, O'Riain, C., additional, Stam, T., additional, Jurgenliemk-Schulz, I., additional, Hamann, M., additional, Smit, V., additional, Bosse, T., additional, and Creutzberg, C., additional
- Published
- 2023
- Full Text
- View/download PDF
3. OC-0601 Early toxicity and quality of life after molecular-based adjuvant treatment in the PORTEC-4a trial
- Author
-
van den Heerik, A., primary, Post, C., additional, Lutgens, L., additional, Haverkort, D., additional, Kommoss, S., additional, Koppe, F., additional, Nowee, M., additional, Westerveld, H., additional, de Jong, M., additional, Cibula, D., additional, Cnossen, J., additional, Mens, J.W., additional, Chargari, C., additional, Bijmolt, S., additional, Gillham, C., additional, Stam, T., additional, Jurgenliemk-Schulz, I., additional, Vandecasteele, K., additional, Verhoeven-Adema, K., additional, Nout, R., additional, Putter, H., additional, Smit, V., additional, Horeweg, N., additional, Bosse, T., additional, and Creutzberg, C., additional
- Published
- 2023
- Full Text
- View/download PDF
4. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial
- Author
-
de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, D'Amico, R, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Gribaudo, S, Provencher, D, Hanzen, C, Kruitwagen, R, Smit, V, Singh, N, Do, V, Lissoni, A, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Lutgens, L, Hollema, H, Pras, E, Snyers, A, Westerveld, G, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen-Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Colombo, A, Carinelli, S, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, Tubiana-Mathieu, N, de Boer S. M., Powell M. E., Mileshkin L., Katsaros D., Bessette P., Haie-Meder C., Ottevanger P. B., Ledermann J. A., Khaw P., D'Amico R., Fyles A., Baron M. -H., Jurgenliemk-Schulz I. M., Kitchener H. C., Nijman H. W., Wilson G., Brooks S., Gribaudo S., Provencher D., Hanzen C., Kruitwagen R. F., Smit V. T. H. B. M., Singh N., Do V., Lissoni A., Nout R. A., Feeney A., Verhoeven-Adema K. W., Putter H., Creutzberg C. L., McCormack M., Whitmarsh K., Allerton R., Gregory D., Symonds P., Hoskin P. J., Adusumalli M., Anand A., Wade R., Stewart A., Taylor W., Lutgens L. C. H. W., Hollema H., Pras E., Snyers A., Westerveld G. H., Jobsen J. J., Slot A., Mens J. M., Stam T. C., Van Triest B., Van der Steen-Banasik E. M., De Winter K. A. J., Quinn M. A., Kolodziej I., Pyman J., Johnson C., Capp A., Fossati R., Colombo A., Carinelli S., Ferrero A., Artioli G., Davidson C., McLachlin C. M., Ghatage P., Rittenberg P. V. C., Souhami L., Thomas G., Duvillard P., Berton-Rigaud D., Tubiana-Mathieu N., de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, D'Amico, R, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Gribaudo, S, Provencher, D, Hanzen, C, Kruitwagen, R, Smit, V, Singh, N, Do, V, Lissoni, A, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Lutgens, L, Hollema, H, Pras, E, Snyers, A, Westerveld, G, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen-Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Colombo, A, Carinelli, S, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, Tubiana-Mathieu, N, de Boer S. M., Powell M. E., Mileshkin L., Katsaros D., Bessette P., Haie-Meder C., Ottevanger P. B., Ledermann J. A., Khaw P., D'Amico R., Fyles A., Baron M. -H., Jurgenliemk-Schulz I. M., Kitchener H. C., Nijman H. W., Wilson G., Brooks S., Gribaudo S., Provencher D., Hanzen C., Kruitwagen R. F., Smit V. T. H. B. M., Singh N., Do V., Lissoni A., Nout R. A., Feeney A., Verhoeven-Adema K. W., Putter H., Creutzberg C. L., McCormack M., Whitmarsh K., Allerton R., Gregory D., Symonds P., Hoskin P. J., Adusumalli M., Anand A., Wade R., Stewart A., Taylor W., Lutgens L. C. H. W., Hollema H., Pras E., Snyers A., Westerveld G. H., Jobsen J. J., Slot A., Mens J. M., Stam T. C., Van Triest B., Van der Steen-Banasik E. M., De Winter K. A. J., Quinn M. A., Kolodziej I., Pyman J., Johnson C., Capp A., Fossati R., Colombo A., Carinelli S., Ferrero A., Artioli G., Davidson C., McLachlin C. M., Ghatage P., Rittenberg P. V. C., Souhami L., Thomas G., Duvillard P., Berton-Rigaud D., and Tubiana-Mathieu N.
- Abstract
Background: The PORTEC-3 trial investigated the benefit of combined adjuvant chemotherapy and radiotherapy versus pelvic radiotherapy alone for women with high-risk endometrial cancer. We updated the analysis to investigate patterns of recurrence and did a post-hoc survival analysis. Methods: In the multicentre randomised phase 3 PORTEC-3 trial, women with high-risk endometrial cancer were eligible if they had International Federation of Gynaecology and Obstetrics (FIGO) 2009 stage I, endometrioid grade 3 cancer with deep myometrial invasion or lymphovascular space invasion, or both; stage II or III disease; or stage I–III disease with serous or clear cell histology; were aged 18 years and older; and had a WHO performance status of 0–2. Participants were randomly assigned (1:1) to receive radiotherapy alone (48·6 Gy in 1·8 Gy fractions given on 5 days per week) or chemoradiotherapy (two cycles of cisplatin 50 mg/m2 given intravenously during radiotherapy, followed by four cycles of carboplatin AUC5 and paclitaxel 175 mg/m2 given intravenously), by use of a biased coin minimisation procedure with stratification for participating centre, lymphadenectomy, stage, and histological type. The co-primary endpoints were overall survival and failure-free survival. Secondary endpoints of vaginal, pelvic, and distant recurrence were analysed according to the first site of recurrence. Survival endpoints were analysed by intention-to-treat, and adjusted for stratification factors. Competing risk methods were used for failure-free survival and recurrence. We did a post-hoc analysis to analyse patterns of recurrence with 1 additional year of follow-up. The study was closed on Dec 20, 2013; follow-up is ongoing. This study is registered with ISRCTN, number ISRCTN14387080, and ClinicalTrials.gov, number NCT00411138. Findings: Between Nov 23, 2006, and Dec 20, 2013, 686 women were enrolled, of whom 660 were eligible and evaluable (330 in the chemoradiotherapy group, and 330 in the rad
- Published
- 2019
5. A Machine-Learning Based Method for Inter-Institutional QA of MR-Based Brachytherapy Treatment Planning in Cervical Cancer
- Author
-
Reijtenbagh, D.M.W., primary, Godart, J., additional, De Leeuw, A., additional, Seppenwoolde, Y., additional, Jurgenliemk-Schulz, I., additional, Mens, J.W.M., additional, and Hoogeman, M.S., additional
- Published
- 2021
- Full Text
- View/download PDF
6. 577 Molecular features and prognostic impact of MELF type myometrial invasion in the PORTEC-1/2 cohort of early stage endometrial cancers
- Author
-
Van den Heerik, AS, primary, Aiyer, K, additional, Jurgenliemk-Schulz, I, additional, Jobsen, J, additional, Mens, JW, additional, Lutgens, L, additional, Nout, R, additional, Creutzberg, CL, additional, Smit, V, additional, Horeweg, N, additional, and Bosse, T, additional
- Published
- 2021
- Full Text
- View/download PDF
7. Importance of training in external beam treatment planning for locally advanced cervix cancer
- Author
-
Seppenwoolde, Y., Assenholt, M.S., Georg, D., Nout, R., Tan, L.T., Rumpold, T., Leeuw, A. de, Jurgenliemk-Schulz, I., Kirisits, C., Potter, R., Lindegaard, J.C., Tanderup, K., EMBRACE Collaborative Grp, and Radiotherapy
- Subjects
medicine.medical_specialty ,Dummy run ,Computer science ,medicine.medical_treatment ,Brachytherapy ,Uterine Cervical Neoplasms ,Plan (drawing) ,EBRT treatment planning ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,SDG 3 - Good Health and Well-being ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Medical physics ,External beam radiotherapy ,EMBRACE II ,Radiation treatment planning ,QA ,Accreditation ,Protocol (science) ,Contouring ,Radiotherapy Planning, Computer-Assisted ,Radiotherapy Dosage ,Hematology ,3. Good health ,Oncology ,Lymphatic Metastasis ,030220 oncology & carcinogenesis ,Female ,Median body ,Lymph Nodes ,Radiotherapy, Image-Guided - Abstract
Background and purpose: The EMBRACE II study combines state-of-the-art Image-Guided Adaptive Brachytherapy in cervix cancer with an advanced protocol for external beam radiotherapy (EBRT) which specifies target volume selection, contouring and treatment planning. In EMBRACE II, well-defined EBRT is an integral part of the overall treatment strategy with the primary aim of improving nodal control and reducing morbidity. The EMBRACE II EBRT planning concept is based on improved conformality through relaxed coverage criteria for all target volumes. For boosting of lymph nodes, a simultaneous integrated boost and coverage probability planning is applied. Before entering EMBRACE II, institutes had to go through accreditation. Material and methods: As part of accreditation, a treatment planning dummy-run included educational blocks and submission of an examination case provided by the study coordinators. Seventy-one centers submitted 123 EBRT dose distributions. Replanning was required if hard constraints were violated or planning concepts were not fully accomplished. Dosimetric parameters of original and revised plans were compared. Results: Only 11 plans violated hard constraints. Twenty-seven centers passed after first submission. 27 needed one and 13 centers needed more revisions. The most common reasons for revisions were low conformality, relatively high OAR doses or insufficient lymph node coverage reduction. Individual feedback on planning concepts improved plan quality considerably, resulting in a median body V43Gy reduction of 158 cm 3 from first plan submission to approved plan. Conclusion: A dummy-run as applied in EMBRACE II, consisting of training and examination cases enabled us to test institutes’ treatment planning capabilities, and improve plan quality.
- Published
- 2019
- Full Text
- View/download PDF
8. OC-0298 Toxicity and patient-reported symptoms after 3D-conformal or intensity-modulated pelvic radiotherapy
- Author
-
Wortman, B., primary, Post, C., additional, Powell, M., additional, Khaw, P., additional, Fyles, A., additional, D’Amico, R., additional, Haie-Meder, C., additional, Jurgenliemk-Schulz, I., additional, McCormack, M., additional, Do, V., additional, Katsaros, D., additional, Bessette, P., additional, Baron, M., additional, Nout, R., additional, Whitmarsh, K., additional, Mileshkin, L., additional, Lutgens, L., additional, Kitchener, H., additional, Brooks, S., additional, Nijman, H., additional, Astreinidou, E., additional, Putter, H., additional, Creutzberg, C., additional, and de Boer, S., additional
- Published
- 2021
- Full Text
- View/download PDF
9. SP-0126 Guideline development GEC ESTRO
- Author
-
Strnad, V., primary, Perez-Calatayud, J., additional, and Jurgenliemk-Schulz, I., additional
- Published
- 2021
- Full Text
- View/download PDF
10. A Machine-Learning Based Method for Inter-Institutional QA of MR-Based Brachytherapy Treatment Planning in Cervical Cancer
- Author
-
Klinische Fysica RT, Cancer, MS Radiotherapie, Reijtenbagh, D. M.W., Godart, J., De Leeuw, A., Seppenwoolde, Y., Jurgenliemk-Schulz, I., Mens, J. W.M., Hoogeman, M. S., Klinische Fysica RT, Cancer, MS Radiotherapie, Reijtenbagh, D. M.W., Godart, J., De Leeuw, A., Seppenwoolde, Y., Jurgenliemk-Schulz, I., Mens, J. W.M., and Hoogeman, M. S.
- Published
- 2021
11. Outcomes & predictors of progression: SBRT for lymph node oligorecurrent prostate cancer on PSMA-PET
- Author
-
Onderzoek Radiotherapie, Cancer, Arts-assistenten Radiotherapie, Klinische Fysica RT, MS Radiotherapie, Werensteijn-Honingh, A., Wevers, A., Peters, M., Kroon, P., Intven, M., Eppinga, W., Jurgenliemk-Schulz, I., Onderzoek Radiotherapie, Cancer, Arts-assistenten Radiotherapie, Klinische Fysica RT, MS Radiotherapie, Werensteijn-Honingh, A., Wevers, A., Peters, M., Kroon, P., Intven, M., Eppinga, W., and Jurgenliemk-Schulz, I.
- Published
- 2021
12. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial
- Author
-
de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, Colombo, A, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Carinelli, S, Provencher, D, Hanzen, C, Lutgens, L, Smit, V, Singh, N, Do, V, D'Amico, R, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Kruitwagen, R, Hollema, H, Pras, E, Snyers, A, Stalpers, L, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen - Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Gribaudo, S, Lissoni, A, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, Tubiana-Mathieu, N, de Boer S. M., Powell M. E., Mileshkin L., Katsaros D., Bessette P., Haie-Meder C., Ottevanger P. B., Ledermann J. A., Khaw P., Colombo A., Fyles A., Baron M. -H., Jurgenliemk-Schulz I. M., Kitchener H. C., Nijman H. W., Wilson G., Brooks S., Carinelli S., Provencher D., Hanzen C., Lutgens L. C. H. W., Smit V. T. H. B. M., Singh N., Do V., D'Amico R., Nout R. A., Feeney A., Verhoeven-Adema K. W., Putter H., Creutzberg C. L., McCormack M., Whitmarsh K., Allerton R., Gregory D., Symonds P., Hoskin P. J., Adusumalli M., Anand A., Wade R., Stewart A., Taylor W., Kruitwagen R. F. P. M., Hollema H., Pras E., Snyers A., Stalpers L., Jobsen J. J., Slot A., Mens J. -W. M., Stam T. C., Van Triest B., Van der Steen - Banasik E. M., De Winter K. A. J., Quinn M. A., Kolodziej I., Pyman J., Johnson C., Capp A., Fossati R., Gribaudo S., Lissoni A. A., Ferrero A., Artioli G., Davidson C., McLachlin C. M., Ghatage P., Rittenberg P. V. C., Souhami L., Thomas G., Duvillard P., Berton-Rigaud D., Tubiana-Mathieu N., de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, Colombo, A, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Carinelli, S, Provencher, D, Hanzen, C, Lutgens, L, Smit, V, Singh, N, Do, V, D'Amico, R, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Kruitwagen, R, Hollema, H, Pras, E, Snyers, A, Stalpers, L, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen - Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Gribaudo, S, Lissoni, A, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, Tubiana-Mathieu, N, de Boer S. M., Powell M. E., Mileshkin L., Katsaros D., Bessette P., Haie-Meder C., Ottevanger P. B., Ledermann J. A., Khaw P., Colombo A., Fyles A., Baron M. -H., Jurgenliemk-Schulz I. M., Kitchener H. C., Nijman H. W., Wilson G., Brooks S., Carinelli S., Provencher D., Hanzen C., Lutgens L. C. H. W., Smit V. T. H. B. M., Singh N., Do V., D'Amico R., Nout R. A., Feeney A., Verhoeven-Adema K. W., Putter H., Creutzberg C. L., McCormack M., Whitmarsh K., Allerton R., Gregory D., Symonds P., Hoskin P. J., Adusumalli M., Anand A., Wade R., Stewart A., Taylor W., Kruitwagen R. F. P. M., Hollema H., Pras E., Snyers A., Stalpers L., Jobsen J. J., Slot A., Mens J. -W. M., Stam T. C., Van Triest B., Van der Steen - Banasik E. M., De Winter K. A. J., Quinn M. A., Kolodziej I., Pyman J., Johnson C., Capp A., Fossati R., Gribaudo S., Lissoni A. A., Ferrero A., Artioli G., Davidson C., McLachlin C. M., Ghatage P., Rittenberg P. V. C., Souhami L., Thomas G., Duvillard P., Berton-Rigaud D., and Tubiana-Mathieu N.
- Abstract
Background: Although women with endometrial cancer generally have a favourable prognosis, those with high-risk disease features are at increased risk of recurrence. The PORTEC-3 trial was initiated to investigate the benefit of adjuvant chemotherapy during and after radiotherapy (chemoradiotherapy) versus pelvic radiotherapy alone for women with high-risk endometrial cancer. Methods: PORTEC-3 was an open-label, international, randomised, phase 3 trial involving 103 centres in six clinical trials collaborating in the Gynaecological Cancer Intergroup. Eligible women had high-risk endometrial cancer with FIGO 2009 stage I, endometrioid-type grade 3 with deep myometrial invasion or lymph-vascular space invasion (or both), endometrioid-type stage II or III, or stage I to III with serous or clear cell histology. Women were randomly assigned (1:1) to receive radiotherapy alone (48·6 Gy in 1·8 Gy fractions given on 5 days per week) or radiotherapy and chemotherapy (consisting of two cycles of cisplatin 50 mg/m2 given during radiotherapy, followed by four cycles of carboplatin AUC5 and paclitaxel 175 mg/m2) using a biased-coin minimisation procedure with stratification for participating centre, lymphadenectomy, stage of cancer, and histological type. The co-primary endpoints were overall survival and failure-free survival. We used the Kaplan-Meier method, log-rank test, and Cox regression analysis for final analysis by intention to treat and adjusted for stratification factors. The study was closed on Dec 20, 2013, after achieving complete accrual; follow-up is ongoing. PORTEC-3 is registered with ISRCTN, number ISRCTN14387080, and ClinicalTrials.gov, number NCT00411138. Results: 686 women were enrolled between Nov 23, 2006, and Dec 20, 2013. 660 eligible patients were included in the final analysis, of whom 330 were assigned to chemoradiotherapy and 330 were assigned to radiotherapy. Median follow-up was 60·2 months (IQR 48·1–73·1). 5-year overall survival was 81·8% (95% CI
- Published
- 2018
13. The EMBRACE II study: The outcome and prospect of two decades of evolution within the GEC-ESTRO GYN working group and the EMBRACE studies
- Author
-
Potter, R., Tanderup, K., Kirisits, C., Leeuw, A. de, Kirchheiner, K., Nout, R., Tan, L.T., Haie-Meder, C., Mahantshetty, U., Segedin, B., Hoskin, P., Bruheim, K., Rai, B., Huang, F., Limbergen, E. van, Schmid, M., Nesvacil, N., Sturdza, A., Fokdal, L., Jensen, N.B.K., Georg, D., Assenholt, M., Seppenwoolde, Y., Nomden, C., Fortin, I., Chopra, S., Heide, U. van der, Rumpold, T., Lindegaard, J.C., Jurgenliemk-Schulz, I., Dumas, I., Chargari, C., Swamidas, J., Shrivastava, S.K., Lowe, G., Hudej, R., Hellebust, T.P., Menon, G., Oinam, A.S., Cooper, R., Bownes, P., Banasik, E.V., Sundset, M., Pieters, B., Lutgens, L.C.H.W., Villafranca, E., Hadjiev, J., Bachand, F., Erickson, B., Jacobson, G., Anttila, M., and EMBRACE Collaborative Grp
- Subjects
medicine.medical_specialty ,STANDARDIZED UPTAKE VALUE ,MODULATED RADIATION-THERAPY ,medicine.medical_treatment ,Brachytherapy ,R895-920 ,Translational research ,LATE RECTAL TOXICITY ,Article ,030218 nuclear medicine & medical imaging ,Medical physics. Medical radiology. Nuclear medicine ,03 medical and health sciences ,0302 clinical medicine ,SDG 3 - Good Health and Well-being ,RATE INTRACAVITARY BRACHYTHERAPY ,Cervix cancer ,QUALITY-OF-LIFE ,CARBON ION RADIOTHERAPY ,ADVANCED CERVICAL-CANCER ,Medicine ,Radiology, Nuclear Medicine and imaging ,Medical physics ,External beam radiotherapy ,Medical prescription ,RC254-282 ,ComputingMethodologies_COMPUTERGRAPHICS ,DOSE-VOLUME PARAMETERS ,Image-guided radiation therapy ,Cervical cancer ,Contouring ,Manchester Cancer Research Centre ,business.industry ,ResearchInstitutes_Networks_Beacons/mcrc ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,GUIDED ADAPTIVE BRACHYTHERAPY ,MRI guided radiotherapy ,medicine.disease ,3. Good health ,Adaptive radiotherapy ,Oncology ,EXTERNAL-BEAM RADIOTHERAPY ,Local control ,030220 oncology & carcinogenesis ,Observational study ,Morbidity ,business - Abstract
Graphical abstract, Highlights • Image guided adaptive brachytherapy (IGABT) is changing clinical practice. • The EMBRACE studies benchmark IGABT in cervix cancer. • A multi-parametric dose prescription protocol is being validated in EMBRACE II. • EMBRACE II is hypothesised to improve outcome: disease, morbidity, quality of life., The publication of the GEC-ESTRO recommendations one decade ago was a significant step forward for reaching international consensus on adaptive target definition and dose reporting in image guided adaptive brachytherapy (IGABT) in locally advanced cervical cancer. Since then, IGABT has been spreading, particularly in Europe, North America and Asia, and the guidelines have proved their broad acceptance and applicability in clinical practice. However, a unified approach to volume contouring and reporting does not imply a unified administration of treatment, and currently both external beam radiotherapy (EBRT) and IGABT are delivered using a large variety of techniques and prescription/fractionation schedules. With IGABT, local control is excellent in limited and well-responding tumours. The major challenges are currently loco-regional control in advanced tumours, treatment-related morbidity, and distant metastatic disease. Emerging evidence from the RetroEMBRACE and EMBRACE I studies has demonstrated that clinical outcome is related to dose prescription and technique. The next logical step is to demonstrate excellent clinical outcome with the most advanced EBRT and brachytherapy techniques based on an evidence-based prospective dose and volume prescription protocol. The EMBRACE II study is an interventional and observational multicentre study which aims to benchmark a high level of local, nodal and systemic control while limiting morbidity, using state of the art treatment including an advanced target volume selection and contouring protocol for EBRT and brachytherapy, a multi-parametric brachytherapy dose prescription protocol (clinical validation of dose constraints), and use of advanced EBRT (IMRT and IGRT) and brachytherapy (IC/IS) techniques (clinical validation). The study also incorporates translational research including imaging and tissue biomarkers.
- Published
- 2018
- Full Text
- View/download PDF
14. Vaginal Dose Surface Maps and Morbidity in Cervical Cancer Brachytherapy
- Author
-
Serban, M., primary, De Leeuw, A., additional, Tanderup, K., additional, and Jurgenliemk-Schulz, I., additional
- Published
- 2020
- Full Text
- View/download PDF
15. Adjuvant chemoradiotherapy versus radiotherapy alone for women with high-risk endometrial cancer (PORTEC-3): final results of an international, open-label, multicentre, randomised, phase 3 trial
- Author
-
de Boer S. M., Powell M. E., Mileshkin L., Katsaros D., Bessette P., Haie-Meder C., Ottevanger P. B., Ledermann J. A., Khaw P., Colombo A., Fyles A., Baron M. -H., Jurgenliemk-Schulz I. M., Kitchener H. C., Nijman H. W., Wilson G., Brooks S., Carinelli S., Provencher D., Hanzen C., Lutgens L. C. H. W., Smit V. T. H. B. M., Singh N., Do V., D'Amico R., Nout R. A., Feeney A., Verhoeven-Adema K. W., Putter H., Creutzberg C. L., McCormack M., Whitmarsh K., Allerton R., Gregory D., Symonds P., Hoskin P. J., Adusumalli M., Anand A., Wade R., Stewart A., Taylor W., Kruitwagen R. F. P. M., Hollema H., Pras E., Snyers A., Stalpers L., Jobsen J. J., Slot A., Mens J. -W. M., Stam T. C., Van Triest B., Van der Steen - Banasik E. M., De Winter K. A. J., Quinn M. A., Kolodziej I., Pyman J., Johnson C., Capp A., Fossati R., Gribaudo S., Lissoni A. A., Ferrero A., Artioli G., Davidson C., McLachlin C. M., Ghatage P., Rittenberg P. V. C., Souhami L., Thomas G., Duvillard P., Berton-Rigaud D., Tubiana-Mathieu N., de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, Colombo, A, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Carinelli, S, Provencher, D, Hanzen, C, Lutgens, L, Smit, V, Singh, N, Do, V, D'Amico, R, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Kruitwagen, R, Hollema, H, Pras, E, Snyers, A, Stalpers, L, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen - Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Gribaudo, S, Lissoni, A, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, and Tubiana-Mathieu, N
- Subjects
Canada ,Antineoplastic Combined Chemotherapy Protocol ,Paclitaxel ,Time Factor ,Risk Factor ,Australia ,Chemoradiotherapy, Adjuvant ,Middle Aged ,Carboplatin ,Europe ,Treatment Outcome ,Gynecologic Surgical Procedures ,Lymph Node Excision ,Endometrial Neoplasm ,Female ,Radiotherapy, Adjuvant ,Dose Fractionation, Radiation ,Cisplatin ,Neoplasm Grading ,Carcinoma, Endometrioid ,Aged ,Human ,Neoplasm Staging ,New Zealand - Abstract
Background: Although women with endometrial cancer generally have a favourable prognosis, those with high-risk disease features are at increased risk of recurrence. The PORTEC-3 trial was initiated to investigate the benefit of adjuvant chemotherapy during and after radiotherapy (chemoradiotherapy) versus pelvic radiotherapy alone for women with high-risk endometrial cancer. Methods: PORTEC-3 was an open-label, international, randomised, phase 3 trial involving 103 centres in six clinical trials collaborating in the Gynaecological Cancer Intergroup. Eligible women had high-risk endometrial cancer with FIGO 2009 stage I, endometrioid-type grade 3 with deep myometrial invasion or lymph-vascular space invasion (or both), endometrioid-type stage II or III, or stage I to III with serous or clear cell histology. Women were randomly assigned (1:1) to receive radiotherapy alone (48·6 Gy in 1·8 Gy fractions given on 5 days per week) or radiotherapy and chemotherapy (consisting of two cycles of cisplatin 50 mg/m2 given during radiotherapy, followed by four cycles of carboplatin AUC5 and paclitaxel 175 mg/m2) using a biased-coin minimisation procedure with stratification for participating centre, lymphadenectomy, stage of cancer, and histological type. The co-primary endpoints were overall survival and failure-free survival. We used the Kaplan-Meier method, log-rank test, and Cox regression analysis for final analysis by intention to treat and adjusted for stratification factors. The study was closed on Dec 20, 2013, after achieving complete accrual; follow-up is ongoing. PORTEC-3 is registered with ISRCTN, number ISRCTN14387080, and ClinicalTrials.gov, number NCT00411138. Results: 686 women were enrolled between Nov 23, 2006, and Dec 20, 2013. 660 eligible patients were included in the final analysis, of whom 330 were assigned to chemoradiotherapy and 330 were assigned to radiotherapy. Median follow-up was 60·2 months (IQR 48·1–73·1). 5-year overall survival was 81·8% (95% CI 77·5–86·2) with chemoradiotherapy versus 76·7% (72·1–81·6) with radiotherapy (adjusted hazard ratio [HR] 0·76, 95% CI 0·54–1·06; p=0·11); 5-year failure-free survival was 75·5% (95% CI 70·3–79·9) versus 68·6% (63·1–73·4; HR 0·71, 95% CI 0·53–0·95; p=0·022). Grade 3 or worse adverse events during treatment occurred in 198 (60%) of 330 who received chemoradiotherapy versus 41 (12%) of 330 patients who received radiotherapy (p
- Published
- 2018
16. 'First in man' treatments with the MRI-linac provide clinical proof of the concept
- Author
-
Jurgenliemk-Schulz, I. M., Raaymakers, B. W., Van Asselen, B., Bol, G. H., Brown, K. J., Doornaert, P., De Groot-van Breugel, E. N., Hackett, S. L., Kasperts, N., Kiekebosch, I. H., Kerkmeijer, L. G. W., Kok, J. G. M., Kotte, A. N. T., Meijers, L. T. C., Nomden, C. N., Pais, B. R., Philippens, M. E. P., Sikkes, G. G., Tersteeg, J. H. A., Tijssen, R. H. N., Wolthaus, J. W. H., Woodings, S. J., and Lagendijk, J. J. W.
- Published
- 2018
17. 1.5T MRI-Linac treatment planning for multiple lymph node oligometastases in the pelvic area
- Author
-
Kiekebosch, I. H., Winkel, D., Werensteijn-Honingh, A. M., Hes, J., Intven, M. P. W., Eppinga, W. S. C., Bol, G. H., Raaymakers, B. W., Jurgenliemk-Schulz, I. M., and Kroon, P. S.
- Published
- 2018
18. Dose escalation and hypofractionation for SBRT of lymph node oligometastases on the 1.5T MRI-Linac
- Author
-
Winkel, D., Bol, G., Werensteijn-Honingh, A., Kiekebosch, I., Hes, J., Intven, M., Eppinga, W., Raaymakers, B., Jurgenliemk-Schulz, I., and Kroon, P.
- Published
- 2018
19. Nomograms Predicting Overall Survival in Locally Advanced Cervical Cancer treated by Image Guided Brachytherapy: a Retro-EMBRACE study
- Author
-
Sturdza, A.E., primary, Potter, R., additional, Kossmeier, M., additional, Kirchheiner, K., additional, Mahantshetty, U.M., additional, Haie-Meder, C., additional, Lindegaard, J., additional, Jurgenliemk-Schulz, I., additional, Tan, L.T., additional, Hoskin, P., additional, van Limbergen, E., additional, Gillham, C., additional, Segedin, B., additional, Tharavichitkul, E., additional, Iturre, E. Villafranca, additional, Fokdal, L., additional, and Tanderup, K., additional
- Published
- 2019
- Full Text
- View/download PDF
20. Patterns of Recurrence and Survival in the Randomized Portec-3 Trial of Chemoradiotherapy for High-Risk Endometrial Cancer
- Author
-
de Boer, S., primary, Powell, M.E., additional, Mileshkin, L., additional, Katsaros, D., additional, Bessette, P., additional, Haie-Meder, C., additional, Ottevanger, P.B., additional, Ledermann, J.A., additional, Khaw, P., additional, Colombo, A., additional, Fyles, A., additional, Baron, M.H., additional, Jurgenliemk-Schulz, I., additional, Kitchener, H., additional, Nijman, H.W., additional, Kruitwagen, R.F., additional, Smit, V.T., additional, Nout, R.A., additional, Putter, H., additional, and Creutzberg, C.L., additional
- Published
- 2019
- Full Text
- View/download PDF
21. Sexual Activity and Vaginal Functioning in Patients with Locally Advanced Cervical Cancer following Definitive Radiochemotherapy and Image-Guided Adaptive Brachytherapy (EMBRACE Study)
- Author
-
Kirchheiner, K., primary, Jurgenliemk-Schulz, I., additional, Haie-Meder, C., additional, Lindegaard, J., additional, Sturdza, A.E., additional, Mahantshetty, U.M., additional, Segedin, B., additional, Bruheim, K., additional, Rai, B., additional, Cooper, R., additional, van der Steen-Banas, E., additional, Wiebe, E.M., additional, Sundset, M., additional, van Limbergen, E., additional, Iturre, E. Villafranca, additional, Westerveld, H., additional, Tan, L.T., additional, Tanderup, K., additional, Potter, R., additional, and Nout, R.A., additional
- Published
- 2019
- Full Text
- View/download PDF
22. OC-0176 A systematic analysis of delineation performance seen in EMBRACE-II brachytherapy quality assurance
- Author
-
Duke, S., primary, Pötter, R., additional, Sturdza, A., additional, Schmid, M., additional, Rumpold, T., additional, Mahantshetty, U., additional, Nesvacil, N., additional, De Leeuw, A., additional, Kirisits, C., additional, Tanderup, K., additional, Nout, R., additional, Lindegaard, J., additional, Jurgenliemk-Schulz, I., additional, and Tan, L., additional
- Published
- 2019
- Full Text
- View/download PDF
23. PV-100 Development of plan quality through EBRT dummy run in the EMBRACE-II study for cervical cancer
- Author
-
Seppenwoolde, Y., primary, Assenholt, M. Sanggaard, additional, Georg, D., additional, Nout, R., additional, Tan, L.T., additional, Rumpold, T., additional, De Leeuw, A., additional, Jurgenliemk-Schulz, I., additional, Kirisits, C., additional, Pötter, R., additional, Lindegaard, J.C., additional, and Tanderup, K., additional
- Published
- 2019
- Full Text
- View/download PDF
24. 'First in man' treatments with the MRI-linac provide clinical proof of the concept
- Author
-
MS Radiotherapie, Cancer, Experimentele klinische fysica, Klinische Fysica RT, Fysica Radiotherapie Research, Jurgenliemk-Schulz, I. M., Raaymakers, B. W., Van Asselen, B., Bol, G. H., Brown, K. J., Doornaert, P., De Groot-van Breugel, E. N., Hackett, S. L., Kasperts, N., Kiekebosch, I. H., Kerkmeijer, L. G. W., Kok, J. G. M., Kotte, A. N. T., Meijers, L. T. C., Nomden, C. N., Pais, B. R., Philippens, M. E. P., Sikkes, G. G., Tersteeg, J. H. A., Tijssen, R. H. N., Wolthaus, J. W. H., Woodings, S. J., Lagendijk, J. J. W., MS Radiotherapie, Cancer, Experimentele klinische fysica, Klinische Fysica RT, Fysica Radiotherapie Research, Jurgenliemk-Schulz, I. M., Raaymakers, B. W., Van Asselen, B., Bol, G. H., Brown, K. J., Doornaert, P., De Groot-van Breugel, E. N., Hackett, S. L., Kasperts, N., Kiekebosch, I. H., Kerkmeijer, L. G. W., Kok, J. G. M., Kotte, A. N. T., Meijers, L. T. C., Nomden, C. N., Pais, B. R., Philippens, M. E. P., Sikkes, G. G., Tersteeg, J. H. A., Tijssen, R. H. N., Wolthaus, J. W. H., Woodings, S. J., and Lagendijk, J. J. W.
- Published
- 2018
25. 1.5T MRI-Linac treatment planning for multiple lymph node oligometastases in the pelvic area
- Author
-
Cancer, Onderzoek Radiotherapie, MS Radiotherapie, Klinische Fysica RT, Experimentele klinische fysica, Kiekebosch, I. H., Winkel, D., Werensteijn-Honingh, A. M., Hes, J., Intven, M. P. W., Eppinga, W. S. C., Bol, G. H., Raaymakers, B. W., Jurgenliemk-Schulz, I. M., Kroon, P. S., Cancer, Onderzoek Radiotherapie, MS Radiotherapie, Klinische Fysica RT, Experimentele klinische fysica, Kiekebosch, I. H., Winkel, D., Werensteijn-Honingh, A. M., Hes, J., Intven, M. P. W., Eppinga, W. S. C., Bol, G. H., Raaymakers, B. W., Jurgenliemk-Schulz, I. M., and Kroon, P. S.
- Published
- 2018
26. Dose escalation and hypofractionation for SBRT of lymph node oligometastases on the 1.5T MRI-Linac
- Author
-
Cancer, Klinische Fysica RT, Onderzoek Radiotherapie, MS Radiotherapie, Experimentele klinische fysica, Winkel, D., Bol, G., Werensteijn-Honingh, A., Kiekebosch, I., Hes, J., Intven, M., Eppinga, W., Raaymakers, B., Jurgenliemk-Schulz, I., Kroon, P., Cancer, Klinische Fysica RT, Onderzoek Radiotherapie, MS Radiotherapie, Experimentele klinische fysica, Winkel, D., Bol, G., Werensteijn-Honingh, A., Kiekebosch, I., Hes, J., Intven, M., Eppinga, W., Raaymakers, B., Jurgenliemk-Schulz, I., and Kroon, P.
- Published
- 2018
27. Dose and Volume Parameters for MRI-Guided Cervix Cancer Brachytherapy in the Embrace Trial
- Author
-
Nesvacil, N., primary, Potter, R., additional, Tanderup, K., additional, Dumas, I., additional, Swamidas, J., additional, De Leeuw, A., additional, Hudej, R., additional, Lowe, G., additional, Spampinato, S., additional, Lindegaard, J., additional, Jurgenliemk-Schulz, I., additional, and Kirisits, C., additional
- Published
- 2018
- Full Text
- View/download PDF
28. Nomogram for prediction of outcome for patients with endometrium cancer: a pooled analysis of PORTEC-1 and PORTEC-2 trials
- Author
-
Creutzberg, C. L., Stiphout, R. G. P. M., Nout, R. A., Lutgens, L. C. H. W., Jurgenliemk-Schulz, I. M., Jobsen, J. J., Vincent THBM Smit, and Lambin, P.
- Published
- 2013
29. Favorable long-term results of primary pterygium removal by bare sclera extirpation followed by a single (90)Strontium application
- Author
-
Mourits, M. P., Wyrdeman, H. K., Jurgenliemk-Schulz, I. M., Bidlot, E., Amsterdam institute for Infection and Immunity, and Ophthalmology
- Subjects
eye diseases - Abstract
PURPOSE. To describe and compare long-term (>= 36 months) effects of patients with 86 primary pterygia treated with bare sclera extirpation ( BSE) followed by beta-RT or by sham irradiation. METHODS. Prospective, multicenter, randomized, double-blind study. After BSE of their pterygium, patients were randomized to either beta-RT or sham irradiation. In the case of beta-RT, within 24 hours after the operation, a 90Sr eye applicator was used to deliver 2500 cGy to the sclera surface at a dose rate of between 200 and 250 cGy/min. Sham irradiation was given using the same type of applicator without the 90Sr layer. After treatment, both a masked ophthalmologist and a radiation oncologist performed follow-up examinations. These were continued until either a relapse occurred or at least 36 months had elapsed. RESULTS. Adequate follow-up was available of 86 pterygia in 81 patients, treated between February 1998 and September 2002. Fifty-two (60%) patients were male. The mean age of the patients was 50 years ( range: 24-77). After a follow-up of at least 36 months ( mean: 40 months, SD: 13.9 months), 5 out of 44 eyes (11%) treated with beta-RT showed a recurrence versus 32 out of 42 eyes (76%) treated with sham-RT ( after a mean follow-up of 22 months) (p
- Published
- 2008
30. Vaginal brachytherapy versus external beam pelvic radiotherapy for high-intermediate risk endometrial cancer: long term results of the randomized PORTEC-2 trial
- Author
-
Nout, R., Stephanie M. de Boer, Putter, H., Jurgenliemk-Schulz, I., Jobsen, J., Lutgens, L., Steen-Banasik, E., Mens, J. W., Slot, A., Stenfert-Kroese, M., Verhoeven-Adema, K., Stelloo, E., Bosse, T., Smit, V., and Creutzberg, C.
31. Patterns of recurrence in the randomised PORTEC-3 trial of chemoradiotherapy for endometrial cancer
- Author
-
De Boer, S. M., Powell, M. E., Mileshkin, L., Katsaros, D., Bessette, P., Haie-Meder, C., Ottevanger, P. B., Ledermann, J. A., Khaw, P., Colombo, A., Fyles, A., Baron, M. H., Jurgenliemk-Schulz, I. M., Kitchener, H. C., Nijman, H. W., Wilson, G., Kolodziej, I., Carinelli, S., Lutgens, L. C. H. W., Smit, V. T. H. B. M., Singh, N., Nout, R. A., Verhoeven-Adema, K. W., Putter, H., Creutzberg, C. L., Targeted Gynaecologic Oncology (TARGON), and Translational Immunology Groningen (TRIGR)
32. Adjuvant chemoradiotherapy versus radiotherapy alone in women with high-risk endometrial cancer (PORTEC-3): patterns of recurrence and post-hoc survival analysis of a randomised phase 3 trial
- Author
-
Carien L. Creutzberg, Petronella B. Ottevanger, Annamaria Ferrero, Luis Souhami, Pearly Khaw, GH Westerveld, Diane Provencher, Gillian Thomas, Jan Pyman, V. Do, Annerie Slot, C Davidson, G. Wilson, Stephanie M. de Boer, Peter Hoskin, C M McLachlin, Michael A. Quinn, Deborah Gregory, Remi A. Nout, Hans W. Nijman, J.J. Jobsen, Tanja C. Stam, Vincent T.H.B.M. Smit, K Whitmarsh, Paul Bessette, Roy F.P.M. Kruitwagen, W Taylor, Dionyssios Katsaros, Chantal Hanzen, Henry C Kitchener, M McCormack, Prafull Ghatage, Dominique Berton-Rigaud, J.W.M. Mens, Melanie E Powell, Elisabeth Pras, Jonathan A. Ledermann, Karen W Verhoeven-Adema, Harmen Hollema, Andrea Lissoni, Linda Mileshkin, Anjana Anand, Amanda Feeney, Sergio Gribaudo, Marie-Helene Baron, R Allerton, Hein Putter, Colin D. Johnson, P. Symonds, Ina M. Jürgenliemk-Schulz, Romerai D'Amico, Ilka Kolodziej, M Adusumalli, Naveena Singh, G Artioli, An Snyers, R Wade, Christine Haie-Meder, Roldano Fossati, Nicole Tubiana-Mathieu, Anthony Fyles, Silvestro Carinelli, Anne Capp, Alexandra J. Stewart, Kaj De Winter, B. van Triest, L.C.H.W. Lutgens, Susan Brooks, E. Van der Steen-Banasik, Pierre Duvillard, Pvc Rittenberg, Alessandro Colombo, de Boer, S, Powell, M, Mileshkin, L, Katsaros, D, Bessette, P, Haie-Meder, C, Ottevanger, P, Ledermann, J, Khaw, P, D'Amico, R, Fyles, A, Baron, M, Jurgenliemk-Schulz, I, Kitchener, H, Nijman, H, Wilson, G, Brooks, S, Gribaudo, S, Provencher, D, Hanzen, C, Kruitwagen, R, Smit, V, Singh, N, Do, V, Lissoni, A, Nout, R, Feeney, A, Verhoeven-Adema, K, Putter, H, Creutzberg, C, Mccormack, M, Whitmarsh, K, Allerton, R, Gregory, D, Symonds, P, Hoskin, P, Adusumalli, M, Anand, A, Wade, R, Stewart, A, Taylor, W, Lutgens, L, Hollema, H, Pras, E, Snyers, A, Westerveld, G, Jobsen, J, Slot, A, Mens, J, Stam, T, Van Triest, B, Van der Steen-Banasik, E, De Winter, K, Quinn, M, Kolodziej, I, Pyman, J, Johnson, C, Capp, A, Fossati, R, Colombo, A, Carinelli, S, Ferrero, A, Artioli, G, Davidson, C, Mclachlin, C, Ghatage, P, Rittenberg, P, Souhami, L, Thomas, G, Duvillard, P, Berton-Rigaud, D, Tubiana-Mathieu, N, MUMC+: MA Toegelatenen Obstetrie Gynaecologie (9), MUMC+: MA Obstetrie Gynaecologie (3), MUMC+: MA Arts Assistenten Obstetrie Gynaecologie (9), RS: GROW - R2 - Basic and Translational Cancer Biology, Obstetrie & Gynaecologie, Translational Immunology Groningen (TRIGR), and Targeted Gynaecologic Oncology (TARGON)
- Subjects
0301 basic medicine ,medicine.medical_specialty ,medicine.medical_treatment ,MED/40 - GINECOLOGIA E OSTETRICIA ,MULTICENTER ,THERAPY ,CARCINOMA PATIENTS ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Internal medicine ,medicine ,Survival analysis ,MED/36 - DIAGNOSTICA PER IMMAGINI E RADIOTERAPIA ,III TRIAL ,Manchester Cancer Research Centre ,Performance status ,business.industry ,ResearchInstitutes_Networks_Beacons/mcrc ,Endometrial cancer ,Hazard ratio ,CHEMOTHERAPY ,OPEN-LABEL ,medicine.disease ,Carboplatin ,Women's cancers Radboud Institute for Health Sciences [Radboudumc 17] ,IRRADIATION ,3. Good health ,Radiation therapy ,030104 developmental biology ,Oncology ,chemistry ,Endometrial cancer, radiotherapy, chemotherapy, adjuvant treatment ,030220 oncology & carcinogenesis ,MED/06 - ONCOLOGIA MEDICA ,RADIATION ,Lymphadenectomy ,business ,Chemoradiotherapy - Abstract
BACKGROUND:The PORTEC-3 trial investigated the benefit of combined adjuvant chemotherapy and radiotherapy versus pelvic radiotherapy alone for women with high-risk endometrial cancer. We updated the analysis to investigate patterns of recurrence and did a post-hoc survival analysis.METHODS:In the multicentre randomised phase 3 PORTEC-3 trial, women with high-risk endometrial cancer were eligible if they had International Federation of Gynaecology and Obstetrics (FIGO) 2009 stage I, endometrioid grade 3 cancer with deep myometrial invasion or lymphovascular space invasion, or both; stage II or III disease; or stage I-III disease with serous or clear cell histology; were aged 18 years and older; and had a WHO performance status of 0-2. Participants were randomly assigned (1:1) to receive radiotherapy alone (48·6 Gy in 1·8 Gy fractions given on 5 days per week) or chemoradiotherapy (two cycles of cisplatin 50 mg/m2 given intravenously during radiotherapy, followed by four cycles of carboplatin AUC5 and paclitaxel 175 mg/m2 given intravenously), by use of a biased coin minimisation procedure with stratification for participating centre, lymphadenectomy, stage, and histological type. The co-primary endpoints were overall survival and failure-free survival. Secondary endpoints of vaginal, pelvic, and distant recurrence were analysed according to the first site of recurrence. Survival endpoints were analysed by intention-to-treat, and adjusted for stratification factors. Competing risk methods were used for failure-free survival and recurrence. We did a post-hoc analysis to analyse patterns of recurrence with 1 additional year of follow-up. The study was closed on Dec 20, 2013; follow-up is ongoing. This study is registered with ISRCTN, number ISRCTN14387080, and ClinicalTrials.gov, number NCT00411138.FINDINGS:Between Nov 23, 2006, and Dec 20, 2013, 686 women were enrolled, of whom 660 were eligible and evaluable (330 in the chemoradiotherapy group, and 330 in the radiotherapy-alone group). At a median follow-up of 72·6 months (IQR 59·9-85·6), 5-year overall survival was 81·4% (95% CI 77·2-85·8) with chemoradiotherapy versus 76·1% (71·6-80·9) with radiotherapy alone (adjusted hazard ratio [HR] 0·70 [95% CI 0·51-0·97], p=0·034), and 5-year failure-free survival was 76·5% (95% CI 71·5-80·7) versus 69·1% (63·8-73·8; HR 0·70 [0·52-0·94], p=0·016). Distant metastases were the first site of recurrence in most patients with a relapse, occurring in 78 of 330 women (5-year probability 21·4%; 95% CI 17·3-26·3) in the chemoradiotherapy group versus 98 of 330 (5-year probability 29·1%; 24·4-34·3) in the radiotherapy-alone group (HR 0·74 [95% CI 0·55-0·99]; p=0·047). Isolated vaginal recurrence was the first site of recurrence in one patient (0·3%; 95% CI 0·0-2·1) in both groups (HR 0·99 [95% CI 0·06-15·90]; p=0·99), and isolated pelvic recurrence was the first site of recurrence in three women (0·9% [95% CI 0·3-2·8]) in the chemoradiotherapy group versus four (0·9% [95% CI 0·3-2·8]) in the radiotherapy-alone group (HR 0·75 [95% CI 0·17-3·33]; p=0·71). At 5 years, only one grade 4 adverse event (ileus or obstruction) was reported (in the chemoradiotherapy group). At 5 years, reported grade 3 adverse events did not differ significantly between the two groups, occurring in 16 (8%) of 201 women in the chemoradiotherapy group versus ten (5%) of 187 in the radiotherapy-alone group (p=0·24). The most common grade 3 adverse event was hypertension (in four [2%] women in both groups). At 5 years, grade 2 or worse adverse events were reported in 76 (38%) of 201 women in the chemoradiotherapy group versus 43 (23%) of 187 in the radiotherapy-alone group (p=0·002). Sensory neuropathy persisted more often after chemoradiotherapy than after radiotherapy alone, with 5-year rates of grade 2 or worse neuropathy of 6% (13 of 201 women) versus 0% (0 of 187). No treatment-related deaths were reported.INTERPRETATION:This updated analysis shows significantly improved overall survival and failure-free survival with chemoradiotherapy versus radiotherapy alone. This treatment schedule should be discussed and recommended, especially for women with stage III or serous cancers, or both, as part of shared decision making between doctors and patients. Follow-up is ongoing to evaluate long-term survival.FUNDING:Dutch Cancer Society, Cancer Research UK, National Health and Medical Research Council, Project Grant, Cancer Australia Grant, Italian Medicines Agency, and the Canadian Cancer Society Research Institute.
- Published
- 2019
- Full Text
- View/download PDF
33. RB Loss in p53 Abnormal Endometrial Carcinoma: Histological and Clinicopathological Correlates.
- Author
-
Serbes ED, Horeweg N, Parra-Herran C, van Rijnsoever R, Jobsen JJ, Jurgenliemk-Schulz I, Kuijsters N, Nout RA, Haverkort MAD, Powell ME, Khaw P, Plante M, Genestie C, Nijman HW, Creutzberg CL, Bosse T, and Kramer CJH
- Abstract
Of the four molecular subtypes of endometrial cancer (EC), p53-abnormal (p53abn) EC is associated with abundant copy number alterations (CNAs) and the worst clinical outcome. Patients with p53abn EC have the highest risk of disease recurrence and death, independent of tumor grade and histologic subtype. Currently, all invasive p53abn ECs are considered high risk, and no prognostic biomarkers have yet been found that can aid in clinical management. Here, we aimed to test whether loss of retinoblastoma protein (RB) expression using immunohistochemistry (IHC) has potential for prognostic refinement of p53abn EC. A large cohort of 227 p53abn ECs collected from the PORTEC-1/2/3 clinical trials and the MST cohort study was investigated, and RB loss was identified in 7.0% (n=16/227). RB-lost p53abn ECs were predominantly high-grade endometrioid ECs (n=6, 37.5%) and carcinosarcomas with endometrioid-type epithelial component (n=5, 31.3%). Histologically, RB-lost p53abn EC were typified by high grade nuclear atypia (n=16, 100%), predominantly solid growth pattern (n=15/16, 93.8%), and polypoid growth (n=9/16, 56.3%). Copy number loss involving the RB1 locus was identified in the majority of RB-lost p53abn EC (n=13/14, 92.9%), explaining the loss of RB expression. Comparative analysis also showed that RB-lost p53abn EC were diagnosed at earlier stages than RB-retained p53abn EC (p=0.014). Interestingly, RB-lost p53abn EC showed prolonged time to overall recurrence (p=0.038), even within stage I alone (p=0.040). These findings highlight distinct morphomolecular features in RB-lost p53abn EC and confirm the utility of RB IHC as a surrogate for molecular RB1 alterations. This is the first study to show the potential use of RB in prognostic refinement of p53abn EC, although validation is warranted., (Copyright © 2024. Published by Elsevier Inc.)
- Published
- 2024
- Full Text
- View/download PDF
34. Interpretable deep learning model to predict the molecular classification of endometrial cancer from haematoxylin and eosin-stained whole-slide images: a combined analysis of the PORTEC randomised trials and clinical cohorts.
- Author
-
Fremond S, Andani S, Barkey Wolf J, Dijkstra J, Melsbach S, Jobsen JJ, Brinkhuis M, Roothaan S, Jurgenliemk-Schulz I, Lutgens LCHW, Nout RA, van der Steen-Banasik EM, de Boer SM, Powell ME, Singh N, Mileshkin LR, Mackay HJ, Leary A, Nijman HW, Smit VTHBM, Creutzberg CL, Horeweg N, Koelzer VH, and Bosse T
- Subjects
- Female, Humans, Eosine Yellowish-(YS), Hematoxylin, Pilot Projects, Deep Learning, Endometrial Neoplasms diagnosis, Endometrial Neoplasms genetics, Endometrial Neoplasms pathology
- Abstract
Background: Endometrial cancer can be molecularly classified into POLE
mut , mismatch repair deficient (MMRd), p53 abnormal (p53abn), and no specific molecular profile (NSMP) subgroups. We aimed to develop an interpretable deep learning pipeline for whole-slide-image-based prediction of the four molecular classes in endometrial cancer (im4MEC), to identify morpho-molecular correlates, and to refine prognostication., Methods: This combined analysis included diagnostic haematoxylin and eosin-stained slides and molecular and clinicopathological data from 2028 patients with intermediate-to-high-risk endometrial cancer from the PORTEC-1 (n=466), PORTEC-2 (n=375), and PORTEC-3 (n=393) randomised trials and the TransPORTEC pilot study (n=110), the Medisch Spectrum Twente cohort (n=242), a case series of patients with POLEmut endometrial cancer in the Leiden Endometrial Cancer Repository (n=47), and The Cancer Genome Atlas-Uterine Corpus Endometrial Carcinoma cohort (n=395). PORTEC-3 was held out as an independent test set and a four-fold cross validation was performed. Performance was measured with the macro and class-wise area under the receiver operating characteristic curve (AUROC). Whole-slide images were segmented into tiles of 360 μm resized to 224 × 224 pixels. im4MEC was trained to learn tile-level morphological features with self-supervised learning and to molecularly classify whole-slide images with an attention mechanism. The top 20 tiles with the highest attention scores were reviewed to identify morpho-molecular correlates. Predictions of a nuclear classification deep learning model serve to derive interpretable morphological features. We analysed 5-year recurrence-free survival and explored prognostic refinement by molecular class using the Kaplan-Meier method., Findings: im4MEC attained macro-average AUROCs of 0·874 (95% CI 0·856-0·893) on four-fold cross-validation and 0·876 on the independent test set. The class-wise AUROCs were 0·849 for POLEmut (n=51), 0·844 for MMRd (n=134), 0·883 for NSMP (n=120), and 0·928 for p53abn (n=88). POLEmut and MMRd tiles had a high density of lymphocytes, p53abn tiles had strong nuclear atypia, and the morphology of POLEmut and MMRd endometrial cancer overlapped. im4MEC highlighted a low tumour-to-stroma ratio as a potentially novel characteristic feature of the NSMP class. 5-year recurrence-free survival was significantly different between im4MEC predicted molecular classes in PORTEC-3 (log-rank p<0·0001). The ten patients with aggressive p53abn endometrial cancer that was predicted as MMRd showed inflammatory morphology and appeared to have a better prognosis than patients with correctly predicted p53abn endometrial cancer (p=0·30). The four patients with NSMP endometrial cancer that was predicted as p53abn showed higher nuclear atypia and appeared to have a worse prognosis than patients with correctly predicted NSMP (p=0·13). Patients with MMRd endometrial cancer predicted as POLEmut had an excellent prognosis, as do those with true POLEmut endometrial cancer., Interpretation: We present the first interpretable deep learning model, im4MEC, for haematoxylin and eosin-based prediction of molecular endometrial cancer classification. im4MEC robustly identified morpho-molecular correlates and could enable further prognostic refinement of patients with endometrial cancer., Funding: The Hanarth Foundation, the Promedica Foundation, and the Swiss Federal Institutes of Technology., Competing Interests: Declaration of interests HWN and JJJ declare grants from Merck, NH declares grants from Varian, and VHK declares research funding from Roche, unrelated to the subject of this manuscript. All other authors declare no competing interests., (Copyright © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.)- Published
- 2023
- Full Text
- View/download PDF
35. Brachytherapy training survey among radiation oncology residents in Europe.
- Author
-
Sturdza AE, Stephanides M, Jurgenliemk-Schulz I, Eriksen JG, Benstead K, Hoskin P, Vlad S, Escande A, Corradini S, Knoth J, Westerveld H, Tagliaferri L, Najari-Jamali D, Konat-Baska K, Plesinac V, Tan LT, Nout R, Strnad V, Niehoff P, Pieters BR, Tanderup K, and Kamrava M
- Subjects
- Humans, Clinical Competence, Curriculum, Surveys and Questionnaires, Europe, Brachytherapy, Internship and Residency organization & administration, Radiation Oncology education
- Abstract
We aim to investigate the current state of brachytherapy (BT) training among the radiation oncology trainees in Europe., Material and Methods: A 22-question online survey based on the one by the American Association of Radiation Oncology Residents (2017) with added queries pertinent to training in Europe was sent to 1450 residents in two iterations. These included site-specific training, volume of experience, barriers to training, institutional support, and preferences for further education. Responses to individual statements were given on a 1 to 5 Likert-type scale. The answers were reported by junior (≤3 years of training) and senior years of training (year of training 4/5/6 and junior staff). Descriptive statistics were used to describe frequencies., Results: Residents from 21 European countries participated, 445 (31%) responded. 205 (47%) were senior residents. 60% residents consider that performing BT independently at the end of residency is very or somewhat important. Confidence in joining a brachytherapy practice at the end of residency was high or somewhat high in 34% of senior residents. They reported as barriers to achieving independence in BT to be lack of appropriate didactic/procedural training from supervisors (47%) and decreased case load (31%). 68% reported their program lacks a formal BT curriculum and standardized training assessment., Conclusions: Residents in Europe, feel independent BT practice is very or somewhat important, but do not feel confident they will achieve this goal. To address this gap, efforts are needed to develop and implement a formal and comprehensive BT curriculum with easy access to trained instructors., (Copyright © 2022. Published by Elsevier B.V.)
- Published
- 2022
- Full Text
- View/download PDF
36. Nomogram Predicting Overall Survival in Patients With Locally Advanced Cervical Cancer Treated With Radiochemotherapy Including Image-Guided Brachytherapy: A Retro-EMBRACE Study.
- Author
-
Sturdza AE, Pötter R, Kossmeier M, Kirchheiner K, Mahantshetty U, Haie-Meder C, Lindegaard JC, Jurgenliemk-Schulz I, Tan LT, Hoskin P, van Limbergen E, Gillham C, Segedin B, Tharavichitkul E, Iturre EV, Fokdal LU, Polterauer S, Kirisits C, and Tanderup K
- Subjects
- Adult, Aged, Female, Humans, Middle Aged, Neoplasm Staging, Proportional Hazards Models, Uterine Cervical Neoplasms mortality, Uterine Cervical Neoplasms pathology, Brachytherapy methods, Chemoradiotherapy methods, Nomograms, Radiotherapy, Image-Guided methods, Uterine Cervical Neoplasms therapy
- Abstract
Purpose: To present a nomogram for prediction of overall survival (OS) in patients with locally advanced cervical cancer (LACC) undergoing definitive radiochemotherapy including image-guided adaptive brachytherapy (IGABT)., Methods and Materials: Seven hundred twenty patients with LACC treated with radiochemotherapy including IGABT in 12 institutions (median follow-up 56 months) were analyzed; 248 deaths occurred. Thirteen candidate predictors for OS were a priori chosen on the basis of the literature and expert knowledge. Missing data (7.2%) were imputed using multiple imputation and predictive mean matching. Univariate analysis with a multivariable Cox regression model for OS stratified by center was performed. Stepwise selection of predictive factors with the Akaike Information Criterion was used to obtain a predictive model and construct a nomogram for OS predictions 60 months from diagnosis; this was internally validated by concordance probability as a measure of discrimination and a calibration plot., Results: Thirteen potential predictive factors were evaluated; 10 factors reached statistical significance in univariate analysis (age, Hemoglobin, FIGO Stage
2009 , tumor width, corpus involvement, lymph node involvement, concurrent chemotherapy, dose to 90% of the high-risk clinical target volume, volume of CTV at the first brachytherapy [CTVHR VolumeBT], overall treatment time [OTT]). Four factors were confirmed significant within the multivariable Cox regression model (FIGO Stage2009 , lymph node involvement, concurrent chemotherapy, CTVHR VolumeBT). The predictive model and corresponding nomogram were based on 7 Akaike Information Criterion-selected factors (age, corpus involvement, FIGO Stage2009 , lymph node involvement, concurrent chemotherapy, CTVHR VolumeBT, OTT) and showed promising calibration and discrimination (cross-validated concordance probability c = 0.73)., Conclusions: This is the first nomogram to predict OS in patients with LACC treated with IGABT. In addition to previously reported factors (age, FIGO2009 stage, corpus involvement, chemotherapy delivery, OTT, lymph node involvement), status of primary tumor at the time of brachytherapy seems to be an essential outcome predictor. These results can facilitate individualized tailoring of treatment and patient counseling during the treatment., (Copyright © 2021 Elsevier Inc. All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
37. Gynecologic Cancer InterGroup (GCIG) consensus review for vulvovaginal melanomas.
- Author
-
Leitao MM Jr, Cheng X, Hamilton AL, Siddiqui NA, Jurgenliemk-Schulz I, Mahner S, Åvall-Lundqvist E, Kim K, and Freyer G
- Subjects
- Combined Modality Therapy, Consensus, Female, Humans, Melanoma therapy, Societies, Medical, Vaginal Neoplasms therapy, Vulvar Neoplasms therapy, Medical Oncology, Melanoma pathology, Practice Guidelines as Topic, Vaginal Neoplasms pathology, Vulvar Neoplasms pathology
- Abstract
Vulvovaginal melanomas are rare tumors that account for a small fraction of all vulvovaginal cancers. Biologically, they seem to be similar to mucosal and acral melanomas of other sites. There are limited data specific to vulvovaginal melanomas, especially regarding systemic therapies. Most treatment decisions are based on extrapolation from data regarding cutaneous melanomas of other sites. It is reasonable to follow already established guidelines from other professional groups and societies. Outcomes tend to be worse compared with cutaneous melanomas likely because of the later presentation and physical biological characteristics of these tumors.
- Published
- 2014
- Full Text
- View/download PDF
38. Favorable long-term results of primary pterygium removal by bare sclera extirpation followed by a single 90Strontium application.
- Author
-
Mourits MP, Wyrdeman HK, Jurgenliemk-Schulz IM, and Bidlot E
- Subjects
- Adult, Aged, Aged, 80 and over, Combined Modality Therapy, Double-Blind Method, Female, Follow-Up Studies, Humans, Male, Middle Aged, Prospective Studies, Recurrence, Treatment Outcome, Young Adult, Pterygium radiotherapy, Pterygium surgery, Sclera surgery, Strontium Radioisotopes therapeutic use
- Abstract
Purpose: To describe and compare long-term (> or = 36 months) effects of patients with 86 primary pterygia treated with bare sclera extirpation (BSE) followed by Beta-RT or by sham irradiation., Methods: Prospective, multicenter, randomized, double-blind study. After BSE of their pterygium, patients were randomized to either Beta-RT or sham irradiation. In the case of Beta-RT, within 24 hours after the operation, a 90Sr eye applicator was used to deliver 2500 cGy to the sclera surface at a dose rate of between 200 and 250 cGy/min. Sham irradiation was given using the same type of applicator without the 90Sr layer. After treatment, both a masked ophthalmologist and a radiation oncologist performed follow-up examinations. These were continued until either a relapse occurred or at least 36 months had elapsed., Results: Adequate follow-up was available of 86 pterygia in 81 patients, treated between February 1998 and September 2002. Fifty-two (60%) patients were male. The mean age of the patients was 50 years (range: 24-77). After a follow-up of at least 36 months (mean: 40 months, SD:13.9 months), 5 out of 44 eyes (11%) treated with Beta-RT showed a recurrence versus 32 out of 42 eyes (76%) treated with sham-RT (after a mean follow-up of 22 months) (p<0.001). In the Beta-RT group, 80% were satisfied with the cosmetic result, whereas in the sham group this percentage was 41% (p<0.001). In the Beta-RT group, no scar or a white scar could be detected in 86% of the treated eyes, versus in 24% of the sham irradiated eyes (p<0.001). A change of keratometry (Javal) was seen in 5 patients (12%) following Beta-RT compared to 16 (38%) after sham irradiation (p=0.002). Complications were few: a granuloma was seen in three patients after sham irradiation, mild limitation of abduction in two Beta-RT patients versus in five after sham irradiation, and mild scleromalacia in one Beta-RT patient., Conclusions: Bare sclera extirpation of a pterygium without adjuvant treatment has an unacceptably high recurrence rate and therefore should be considered obsolete. Bare sclera extirpation of a primary pterygium followed by a single-dose Beta-RT is a simple, effective, and safe treatment with lasting results and very few complications.
- Published
- 2008
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.