127 results on '"van Roessel, S"'
Search Results
2. Artificial Intelligence-Based Segmentation of Residual Tumor in Histopathology of Pancreatic Cancer after Neoadjuvant Treatment
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Janssen, B., primary, Theijse, R., additional, van Roessel, S., additional, de Ruiter, R., additional, Berkel, A., additional, Busch, O., additional, Wilmink, J., additional, Kazemier, G., additional, Valkema, P., additional, Farina, A., additional, Verheij, J., additional, de Boer, O., additional, and Besselink, M., additional
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- 2022
- Full Text
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3. Oncological outcomes of minimally-invasive and open pancreatoduodenectomy for pancreatic ductal adenocarcinoma: An international retrospective propensity-score matched study
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Vissers, F., primary, Van Roessel, S., additional, Rosso, E., additional, Kauffmann, E., additional, Klompmaker, S., additional, Alseidi, A., additional, Espopsito, A., additional, Coratti, A., additional, Dokmak, S., additional, Fuks, D., additional, Groot Koerkamp, B., additional, Hackert, T., additional, Halimi, A., additional, Keck, T., additional, Kerem, M., additional, Khatkov, I., additional, Molenaar, Q., additional, Saint-Marc, O., additional, van Santvoort, H., additional, Wittel, U., additional, Wolfgang, C., additional, Abu Hilal, M., additional, Besselink, M., additional, and Boggi, U., additional
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- 2021
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4. Machine learning-based auto-segmentation of histological residual tumor in resected pancreatic cancer after neoadjuvant therapy
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Janssen, B., primary, Theijse, R., additional, van Roessel, S., additional, de Ruiter, R., additional, Berkel, A., additional, Huiskens, J., additional, Busch, O., additional, Wilmink, J., additional, Kazemier, G., additional, Valkema, P., additional, Farina, A., additional, Verheij, J., additional, Besselink, M., additional, and de Boer, O., additional
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- 2021
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5. Hospital costs of delayed gastric emptying following pancreatoduodenectomy and the financial headroom for novel prophylactic treatment strategies
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Francken, M., primary, Van Roessel, S., additional, Swijnenburg, R.-J., additional, Erdmann, J., additional, Busch, O., additional, Dijkgraaf, M., additional, and Besselink, M., additional
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- 2021
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6. External validation of three nomograms predicting survival using an international cohort of patients with resected pancreatic head ductal adenocarcinoma
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Schneider, M, primary, Labgaa, I, additional, Vrochides, D, additional, Zerbi, A, additional, Nappo, G, additional, Perinel, J, additional, Adham, M, additional, van Roessel, S, additional, Besselink, M, additional, Mieog, J S D, additional, Groen, J V, additional, Demartines, N, additional, Schäfer, M, additional, and Joliat, G -R, additional
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- 2021
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7. Axial slicing versus bivalving in the pathological examination of pancreatoduodenectomy specimens (APOLLO): a multicentre randomized controlled trial
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van Roessel, S. (Stijn), Soer, E.C. (Eline C.), Van Dieren, S. (Susan), Koens, L. (Lianne), Velthuysen, M.L.F. (Loes) van, Doukas, M. (Michael), Groot Koerkamp, B. (Bas), Fariña-Sarasqueta, A. (Arantza), Bronkhorst, C.M. (Carolien), Raicu, G.M. (G. Mihaela), Kuijpers, K.C. (Karel C.), Seldenrijk, K.A. (Kees), Santvoort, H.C. (Hjalmar) van, Molenaar, I.Q. (I. Quintus), Van Der Post, R.S. (Rachel S.), Stommel, M.W.J. (Martijn W.J.), Busch, O.R.C. (Olivier), Besselink, M.G. (Marc), Brosens, L.A. (Lodewijk), Verheij, J. (Joanne), van Roessel, S. (Stijn), Soer, E.C. (Eline C.), Van Dieren, S. (Susan), Koens, L. (Lianne), Velthuysen, M.L.F. (Loes) van, Doukas, M. (Michael), Groot Koerkamp, B. (Bas), Fariña-Sarasqueta, A. (Arantza), Bronkhorst, C.M. (Carolien), Raicu, G.M. (G. Mihaela), Kuijpers, K.C. (Karel C.), Seldenrijk, K.A. (Kees), Santvoort, H.C. (Hjalmar) van, Molenaar, I.Q. (I. Quintus), Van Der Post, R.S. (Rachel S.), Stommel, M.W.J. (Martijn W.J.), Busch, O.R.C. (Olivier), Besselink, M.G. (Marc), Brosens, L.A. (Lodewijk), and Verheij, J. (Joanne)
- Abstract
Background: In pancreatoduodenectomy specimens, dissection method may affect the assessment of primary tumour origin (i.e. pancreatic, distal bile duct or ampullary adenocarcinoma), which is primarily determined macroscopically. This is the first study to prospectively compare the two commonly used techniques, i.e. axial slicing and bivalving. Methods: In four centres, a randomized controlled trial was performed in specimens of patients with a suspected (pre)malignant tumour in the pancreatic head. Primary outcome measure was the level of certainty (scale 0–100) regarding tumour origin by four independent gastrointestinal pathologists based on macroscopic assessment. Secondary outcomes were inter-observer agreement and R1 rate. Results: In total, 128 pancreatoduodenectomy specimens were randomized. The level of certainty in determining the primary tumour origin did not differ between axial slicing and bivalving (mean score 72 [sd 13] vs. 68 [sd 16], p = 0.21), nor did inter-observer agreement, both being moderate (kappa 0.45 vs. 0.47). In pancreatic cancer specimens, R1 rate (60% vs. 55%, p = 0.71) and the number of harvested lymph nodes (median 16 vs. 17, p = 0.58) were similar. Conclusion: This study demonstrated no differences in determining the tumour origin between axial slicing and bivalving. Both techniques performed similarly regarding inter-observer agreement, R1 rate, and lymph node harvest.
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- 2021
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8. Scoring of tumour response after neoadjuvant therapy in resected pancreatic cancer: systematic review
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Pathologie Pathologen staf, Cancer, van Roessel, S, Janssen, B V, Soer, E C, Fariña Sarasqueta, A, Verbeke, C S, Luchini, C, Brosens, L A A, Verheij, J, Besselink, M G, Pathologie Pathologen staf, Cancer, van Roessel, S, Janssen, B V, Soer, E C, Fariña Sarasqueta, A, Verbeke, C S, Luchini, C, Brosens, L A A, Verheij, J, and Besselink, M G
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- 2021
9. Scoring of tumour response after neoadjuvant therapy in resected pancreatic cancer: systematic review
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van Roessel, S, primary, Janssen, B V, additional, Soer, E C, additional, Fariña Sarasqueta, A, additional, Verbeke, C S, additional, Luchini, C, additional, Brosens, L A A, additional, Verheij, J, additional, and Besselink, M G, additional
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- 2021
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10. External Validation of Three Nomograms Predicting Survival Using an International Cohort of Patients with Resected Pancreatic Head Ductal Adenocarcinoma
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Schneider, M., primary, Labgaa, I., additional, Vrochides, D., additional, Zerbi, A., additional, Nappo, G., additional, Perinel, J., additional, Adham, M., additional, van Roessel, S., additional, Besselink, M., additional, Mieog, J.S.D., additional, Groen, J.V., additional, Demartines, N., additional, Schäfer, M., additional, and Joliat, G.-R., additional
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- 2021
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11. Lymph Node Ratio as Predictor of Survival in Patients with Resected Pancreatic Ductal Adenocarcinoma
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Joliat, G.-R., primary, Labgaa, I., additional, Sulzer, J., additional, Vrochides, D., additional, Zerbi, A., additional, Nappo, G., additional, Perinel, J., additional, Adham, M., additional, van Roessel, S., additional, Besselink, M., additional, Mieog, J.S.D., additional, Groen, J., additional, Demartines, N., additional, and Schäfer, M., additional
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- 2021
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12. Hospital costs of delayed gastric emptying following pancreatoduodenectomy and the financial headroom for novel prophylactic treatment strategies
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Francken, M.F., primary, van Roessel, S., additional, Swijnenburg, R.-J., additional, Erdmann, J.I., additional, Busch, O.R., additional, Dijkgraaf, M.G., additional, and Besselink, M.G., additional
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- 2021
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13. Conditional Survival During Follow-up after Resection for Pancreatic Cancer: A Population-based Study and Prediction Model
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Latenstein, A., primary, van Roessel, S., additional, van der Geest, L., additional, Wilmink, J., additional, and Besselink, M., additional
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- 2021
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14. Oncological outcome after minimally-invasive or open pancreatoduodenectomy for pancreatic cancer: an international propensity-score matched study
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Vissers, F., primary, van Roessel, S., additional, Klompmaker, S., additional, Abu Hilal, M., additional, Besselink, M., additional, and Boggi, U., additional
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- 2021
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15. Oncological Outcomes of Minimally-invasive and Open Pancreatoduodenectomy for PDAC: An International Retrospective Propensity-score Matched Study
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Vissers, F., primary, van Roessel, S., additional, Rosso, E., additional, Kauffmann, E., additional, Klompmaker, S., additional, Alseidi, A., additional, Coratti, A., additional, Dokmak, S., additional, Espopsito, A., additional, Fuks, D., additional, Groot Koerkamp, B., additional, Hackert, T., additional, Halimi, A., additional, Keck, T., additional, Kerem, M., additional, Khatkov, I., additional, Molenaar, Q., additional, Saint-Marc, O., additional, van Santvoort, H., additional, Wittel, U., additional, Wolfgang, C., additional, Abu Hilal, M., additional, Besselink, M., additional, and Boggi, U., additional
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- 2021
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16. Adjuvant chemotherapy in patients with resected pancreatic cancer following neoadjuvant FOLFIRINOX chemotherapy: an international multicenter study
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Van Roessel, S., primary, Van Veldhuisen, E., additional, Jansen, K., additional, Abu Hilal, M., additional, Alseidi, A., additional, Bassi, C., additional, Malleo, G., additional, Del Chiaro, M., additional, Hackert, T., additional, Falconi, M., additional, Mortensen, M., additional, Lesurtel, M., additional, Keck, T., additional, Pietrasz, D., additional, Strobel, O., additional, Tarvainen, T., additional, Van Laarhoven, H., additional, Wilmink, H., additional, Groot Koerkamp, B., additional, and Besselink, M., additional
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- 2020
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17. Development and internal validation of two nomograms predicting outcomes in patients with locally advanced pancreatic cancer starting treatment with FOLFIRINOX
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Brada, L., primary, Walma, M., additional, Daamen, L., additional, Van Roessel, S., additional, Van Dam, R., additional, De Hingh, I., additional, Liem, M., additional, De Meijer, V., additional, Patijn, G., additional, Festen, S., additional, Stommel, M., additional, Meijerink, M., additional, Bosscha, K., additional, Polée, M., additional, Ropela, A., additional, Nio, Y., additional, Wessels, F., additional, Van Leeuwen, M., additional, De Vries, J., additional, Van Lienden, K., additional, Bruijnen, R., additional, Busch, O., additional, Besselink, M., additional, Molenaar, Q., additional, and Van Santvoort, H., additional
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- 2020
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18. Gemcitabine-based adjuvant chemotherapy in subtypes of ampullary adenocarcinoma: international propensity score-matched cohort study
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Moekotte, A L, primary, Malleo, G, additional, van Roessel, S, additional, Bonds, M, additional, Halimi, A, additional, Zarantonello, L, additional, Napoli, N, additional, Dreyer, S B, additional, Wellner, U F, additional, Bolm, L, additional, Mavroeidis, V K, additional, Robinson, S, additional, Khalil, K, additional, Ferraro, D, additional, Mortimer, M C, additional, Harris, S, additional, Al-Sarireh, B, additional, Fusai, G K, additional, Roberts, K J, additional, Fontana, M, additional, White, S A, additional, Soonawalla, Z, additional, Jamieson, N B, additional, Boggi, U, additional, Alseidi, A, additional, Shablak, A, additional, Wilmink, J W, additional, Primrose, J N, additional, Salvia, R, additional, Bassi, C, additional, Besselink, M G, additional, and Abu Hilal, M, additional
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- 2020
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19. Clinicopathological outcome and prognostication in pancreatic surgery
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van Roessel, S., Besselink, Marc G. H., Busch, Olivier R. C., Verheij, Joanne, Groot Koerkamp, Bas, CCA - Treatment and quality of life, Graduate School, Besselink, M.G.H., Busch, O.R.C., Verheij, J., Groot Koerkamp, B., and Faculteit der Geneeskunde
- Abstract
This thesis mainly encompasses studies aimed to improve oncological and surgical treatment of pancreatic head cancer and other periampullary cancers in relation to short-term clinical and long-term oncological outcome. Many studies are a collaboration between multiple centers, either within the nationwide Dutch Pancreatic Cancer Group (DPCG) or as international collaboration, both within or outside Europe. Part I comprises three chapters, outlining the surgical and oncological outcomes of pancreatic surgery in a single-center study, a nationwide study and an international cohort study. The five chapters in Part II mainly focus on the challenges encountered in the pathology assessment of a surgical specimen following pancreatic surgery. The five chapters in Part III evaluate the prognostic significance of several prediction models and staging systems for pancreatic and other periampullary cancers. The prediction models were made available on the website www.pancreascalculator.com.
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- 2020
20. Textbook Outcome Nationwide Analysis of a Novel Quality Measure in Pancreatic Surgery
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van Roessel, S., Mackay, T.M., van Dieren, S, van der Schelling, GP, Nieuwenhutjs, V.B., Bosscha, K. (Koop), Harst, E. (Erwin) van der, Dam, R.M. (Rob) van, Liem, M.S., Festen, S. (Sebastiaan), Stommel, M.W.J., Roos, D. (Dirk), Wit, F. (Femke) de, Molenaar, I.Q. (I. Quintus), Meijer, V.E. (Vincent) de, Kazemier, G, de Hingh, I., Santvoort, H.C. (Hjalmar) van, Bonsing, B.A. (Bert), Busch, ORC, Groot Koerkamp, B. (Bas), Besselink, M.G. (Marc), van Roessel, S., Mackay, T.M., van Dieren, S, van der Schelling, GP, Nieuwenhutjs, V.B., Bosscha, K. (Koop), Harst, E. (Erwin) van der, Dam, R.M. (Rob) van, Liem, M.S., Festen, S. (Sebastiaan), Stommel, M.W.J., Roos, D. (Dirk), Wit, F. (Femke) de, Molenaar, I.Q. (I. Quintus), Meijer, V.E. (Vincent) de, Kazemier, G, de Hingh, I., Santvoort, H.C. (Hjalmar) van, Bonsing, B.A. (Bert), Busch, ORC, Groot Koerkamp, B. (Bas), and Besselink, M.G. (Marc)
- Abstract
Background: Textbook outcome (TO) is a multidimensional measure for quality assurance, reflecting the ‘‘ideal’’ surgical outcome. Methods: Post-hoc analysis of patients who underwent pancreatoduodenectomy (PD) or distal pancreatectomy (DP) for all indications between 2014 and 2017, queried from the nationwide prospective Dutch Pancreatic Cancer Audit. An international survey was conducted among 24 experts from 10 countries to reach consensus on the requirements for TO in pancreatic surgery. Univariable and multivariable logistic regression was performed to identify TO predictors. Between-hospital variation in TO rates was compared using observed-versus-expected rates. Results: Based on the survey (92% response rate), TO was defined by the absence of postoperative pancreatic fistula, bile leak, postpancreatectomy hemorrhage (all ISGPS grade B/C), severe complications (Clavien–Dindo III), readmission, and in-hospital mortality. Overall, 3341 patients were included (2633 (79%) PD and 708 (21%) DP) of whom 60.3% achieved TO; 58.3% for PD and 67.4% for DP. On multivariable analysis, ASA class 3 predicted a worse TO rate after PD (ASA 3 OR 0.59 [0.44–0.80]), whereas a dilated pancreatic duct (>3 mm) and pancreatic ductal aden
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- 2020
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21. Textbook Outcome Nationwide Analysis of a Novel Quality Measure in Pancreatic Surgery
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van Roessel, S, Mackay, TM, van Dieren, S, van der Schelling, GP, Nieuwenhutjs, VB, Bosscha, K, Harst, E, van Dam, RM, Liem, MS, Festen, S, Stommel, MWJ, Roos, D, de Wit, F, Molenaar, IQ, Meijer, VE, Kazemier, G, de Hingh, I, van Santvoort, HC, Bonsing, BA, Busch, ORC, Groot Koerkamp, B, Besselink, MGH, van Roessel, S, Mackay, TM, van Dieren, S, van der Schelling, GP, Nieuwenhutjs, VB, Bosscha, K, Harst, E, van Dam, RM, Liem, MS, Festen, S, Stommel, MWJ, Roos, D, de Wit, F, Molenaar, IQ, Meijer, VE, Kazemier, G, de Hingh, I, van Santvoort, HC, Bonsing, BA, Busch, ORC, Groot Koerkamp, B, and Besselink, MGH
- Published
- 2020
22. Development of a prediction model for survival in patients with resected ampullary adenocarcinoma: international multicenter study
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Moekotte, A., primary, Van Roessel, S., additional, Fontana, M., additional, Bonds, M., additional, Halimi, A., additional, Zarantonello, L., additional, Napoli, N., additional, Dreyer, S., additional, Casciani, F., additional, Mavroeidis, V., additional, Robinson, S., additional, Khalil, K., additional, Gradinariu, G., additional, Mowbray, N., additional, Al-Sarireh, B., additional, Kito, G., additional, Roberts, K., additional, White, S., additional, Soonawalla, Z., additional, Jamieson, N., additional, Boggi, U., additional, Alseidi, A., additional, Salvia, R., additional, Besselink, M., additional, and Hilal, M Abu, additional
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- 2020
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23. Textbook outcome as a novel quality measure in pancreatic surgery: a nationwide analysis
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Van Roessel, S., primary, Mackay, T., additional, Van Dieren, S., additional, Van der Schelling, G., additional, Nieuwenhuijs, V., additional, Bosscha, K., additional, Van der Harst, E., additional, Van Dam, R., additional, Liem, M., additional, Festen, S., additional, Stommel, M., additional, Roos, D., additional, Wit, F., additional, Molenaar, Q., additional, De Meijer, V., additional, De Hingh, I., additional, Van Santvoort, H., additional, Bonsing, B., additional, Busch, O., additional, Koerkamp, B Groot, additional, and Besselink, M., additional
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- 2020
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24. International validation of a nomogram to predict recurrence after resection of grade 1 and 2 pancreatic neuroendocrine tumors
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Heidsma, C.M., primary, van Roessel, S., additional, van Dieren, S., additional, Engelsman, A.F., additional, Strobel, O., additional, Buechler, M., additional, Schimmack, S., additional, Perinel, J., additional, Adham, M., additional, Deshpande, V., additional, Kjaer, J., additional, Norlen, O., additional, Gill, A.J., additional, Samra, J.S., additional, Mittal, A., additional, Hoogwater, F.J.H., additional, van Eijck, C.H.J., additional, Besselink, M.G., additional, and Nieveen van Dijkum, E.J.M., additional
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- 2020
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25. The benefit of adjuvant chemotherapy in subtypes of ampullary adenocarcinoma: International propensity score matched study
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Moekotte, A., primary, Fontana, M., additional, Van Roessel, S., additional, Bonds, M., additional, Halimi, A., additional, Zarantonello, L., additional, Napoli, N., additional, Dreyer, S., additional, Casciani, F., additional, Mavroeidis, V., additional, Robinson, S., additional, Khalil, K., additional, Gradinariu, G., additional, Mowbray, N., additional, Al-Sarireh, B., additional, Kito, G., additional, Roberts, K., additional, White, S., additional, Soonawalla, Z., additional, Jamieson, N., additional, Boggi, U., additional, Alseidi, A., additional, Shablak, A., additional, Wilmink, J., additional, Primrose, J., additional, Salvia, R., additional, Besselink, M., additional, and Hilal, M Abu, additional
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- 2020
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26. Axial slicing versus bivalving of the pancreatic head in the pathological examination of pancreatoduodenectomy specimens (apollo): A randomized controlled trial
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van Roessel, S., primary, Soer, E., additional, van Dieren, S., additional, Koens, L., additional, van Velthuysen, M., additional, Doukas, M., additional, Koerkamp, B Groot, additional, Sarasqueta, A Fariña, additional, Bronkhorst, C., additional, Raicu, G., additional, Kuijpers, K., additional, Seldenrijk, C., additional, van Santvoort, H., additional, Molenaar, I., additional, van der Post, R., additional, Stommel, M., additional, Busch, O., additional, Besselink, M., additional, Brosens, L., additional, and Ve, J., additional
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- 2020
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27. International validation and update of the Amsterdam model for prediction of survival after pancreatoduodenectomy for pancreatic cancer
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van Roessel, S., primary, Strijker, M., additional, Steyerberg, E., additional, Groen, J., additional, Mieog, J., additional, Groot, V., additional, He, J., additional, De Pastena, M., additional, Marchegiani, G., additional, Bassi, C., additional, Suhool, A., additional, Jang, J., additional, Busch, O., additional, Halimi, A., additional, Zarantonello, L., additional, Groot Koerkamp, B., additional, Samra, J., additional, Mittal, A., additional, Gill, A., additional, Bolm, L., additional, van Eijck, C., additional, Abu Hilal, M., additional, and del Chiar, M., additional
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- 2020
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28. Treatment of mid-bile duct cholangiocarcinoma: Local resection or pancreatoduodenectomy?
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Schreuder, A.M., primary, Engelsman, A., additional, Van Roessel, S., additional, Verheij, J., additional, Besselink, M., additional, Van Gulik, T., additional, and Busch, O., additional
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- 2020
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29. International validation of the Amsterdam model for survival prediction after resected pancreatic cancer
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Van Roessel, S., primary, Strijker, M., additional, Steyerberg, E., additional, Groen, J., additional, Mieog, S., additional, De Pastena, M., additional, Machegiani, G., additional, Jang, J., additional, Busch, O., additional, Halimi, A., additional, Zarantonello, L., additional, Koerkamp, B Groot, additional, Samra, J., additional, Mittal, A., additional, Gill, A., additional, Wellner, U., additional, Van Eijck, C., additional, Hilal, M Abu, additional, Del Chiaro, M., additional, Keck, T., additional, Alseidi, A., additional, Malleo, G., additional, and Besselink, M., additional
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- 2020
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30. Histopathologic predictors of survival and recurrence in resected ampullary adenocarcinoma: International multicenter cohort study
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Moekotte, A.L., primary, Lof, S., additional, van Roessel, S., additional, Fontana, M., additional, Dreyer, S., additional, Shablak, A., additional, Casciani, F., additional, Mavroeidis, V.K., additional, Robinson, S., additional, Khalil, K., additional, Gradinariu, G., additional, Mowbray, N., additional, Al-Sarireh, B., additional, Fusai, G Kito, additional, Roberts, K., additional, White, S.A., additional, Soonawalla, Z., additional, Jamieson, N.B., additional, Salvia, R., additional, Besselink, M.G., additional, and Hilal, M Abu, additional
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- 2019
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31. Textbook outcome as a novel composite quality measure in pancreatic surgery: A nationwide analysis
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van Roessel, S., primary, Mackay, T.M., additional, van Dieren, S., additional, de Hingh, I.H., additional, van Santvoort, H.C., additional, Bonsing, B.A., additional, Busch, O.R., additional, Koerkamp, B Groot, additional, and Besselink, M.G., additional
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- 2019
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32. International validation of the 8th edition American joint committee on cancer (AJCC) TNM staging system in patients with resected pancreatic cancer
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van Roessel, S., primary, Kasumova, G., additional, Verheij, J., additional, de Pastena, M., additional, Groot Koerkamp, B., additional, Abu Hilal, M., additional, van Eijck, C., additional, Tseng, J., additional, Bassi, C., additional, and Besselink, M., additional
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- 2018
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33. Short- and long-term outcomes in 1438 consecutive pancreatoduodenectomies: a single-center 25-years' experience
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van Roessel, S., primary, Mackay, T., additional, Tol, J., additional, van Gulik, T., additional, Gouma, D., additional, Busch, O., additional, and Besselink, M., additional
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- 2018
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34. Accuracy of aPTT monitoring in critically ill patients treated with unfractionated heparin
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van Roessel, S., Middeldorp, S., Cheung, Y. W., Zwinderman, A. H., de Pont, A. C. J. M., ACS - Amsterdam Cardiovascular Sciences, Vascular Medicine, 01 Internal and external specialisms, APH - Amsterdam Public Health, Epidemiology and Data Science, AII - Amsterdam institute for Infection and Immunity, and Intensive Care Medicine
- Subjects
circulatory and respiratory physiology - Abstract
The anticoagulant effect of unfractionated heparin (UFH) is usually monitored by means of the activated partial thromboplastin time (aPTT). In critically ill patients, however, increased levels of acute phase proteins may decrease the accuracy of the aPTT, leading to inadequate UFH dosing. In these circumstances, the anti-Xa assay is recommended for monitoring. We aimed to analyse the accuracy of the aPTT for the monitoring of UFH dosing in critically ill patients. In critically ill patients treated with therapeutic doses of UFH, we compared aPTT levels with simultaneously measured anti-Xa levels as the gold standard. Sensitivity and specificity of the aPTT were determined for different cut-off points, receiver operating characteristic (ROC) curves were constructed and their areas under the curve (AUCs) were calculated. A total of 171 paired blood samples from 58 patients were analysed. Concordant aPTT and anti-Xa values were observed in 108 (63.2%) data pairs. In 33 data pairs (19.3%) the aPTT was discordantly high and in 30 data pairs (17.5%) discordantly low. The sensitivity of the aPTT in detecting UFH underdosing and overdosing was 0.63 and 0.37, respectively. When considering alternative thresholds, ROC curves for underdosing and overdosing had AUCs of 0.71 and 0.81, respectively. In this small cohort of critically ill patients, the aPTT was accurate in 63.2% of the blood samples. Its sensitivity to detect UFH underdosing and overdosing was low (0.63 and 0.37, respectively). We conclude that in critically ill patients, the aPTT is not accurate enough to detect UFH underdosing and overdosing
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- 2014
35. Evaluation of Adjuvant Chemotherapy in Patients With Resected Pancreatic Cancer After Neoadjuvant FOLFIRINOX Treatment
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Marco Del Chiaro, Patrick M.M. Bossuyt, Giuseppe Malleo, Isabella Frigerio, A Nikov, Antonio Sa Cunha, Johan Gagnière, Rupaly Pande, Morgan Bonds, Mickael Lesurtel, Kevin C. Conlon, Per Pfeiffer, Giuseppe Fusai, Marc G. Besselink, Giovanni Butturini, Bas Groot Koerkamp, Claudio Bassi, Sjors Klompmaker, Ulla Klaiber, Stijn van Roessel, Massimo Falconi, Marco Vito Marino, Eran van Veldhuisen, Oonagh Griffin, Michael Bau Mortensen, Mohammed Abu Hilal, Tobias Keck, Timo Tarvainen, Frederik Berrevoet, Oliver Strobel, Asif Halimi, Thilo Hackert, Knut Jørgen Labori, Gianpaolo Balzano, Jörg Kleeff, Olivier R. Busch, Roberto Salvia, D. Pietrasz, Adnan Alseidi, Johanna W. Wilmink, Keith J. Roberts, Quisette P. Janssen, A. Balduzzi, Hanneke W. M. van Laarhoven, Surgery, Graduate School, CCA - Cancer Treatment and Quality of Life, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, APH - Personalized Medicine, APH - Methodology, Epidemiology and Data Science, Oncology, CCA -Cancer Center Amsterdam, Van Roessel, S., Van Veldhuisen, E., Klompmaker, S., Janssen, Q. P., Abu Hilal, M., Alseidi, A., Balduzzi, A., Balzano, G., Bassi, C., Berrevoet, F., Bonds, M., Busch, O. R., Butturini, G., Del Chiaro, M., Conlon, K. C., Falconi, M., Frigerio, I., Fusai, G. K., Gagniere, J., Griffin, O., Hackert, T., Halimi, A., Klaiber, U., Labori, K. J., Malleo, G., Marino, M. V., Mortensen, M. B., Nikov, A., Lesurtel, M., Keck, T., Kleeff, J., Pande, R., Pfeiffer, P., Pietrasz, D., Roberts, K. J., Sa Cunha, A., Salvia, R., Strobel, O., Tarvainen, T., Bossuyt, P. M., Van Laarhoven, H. W. M., Wilmink, J. W., Groot Koerkamp, B., and Besselink, M. G.
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Male ,Cancer Research ,medicine.medical_specialty ,FOLFIRINOX ,Adjuvant Chemotherapy ,medicine.medical_treatment ,Leucovorin ,Irinotecan ,Gastroenterology ,03 medical and health sciences ,Folinic acid ,0302 clinical medicine ,SDG 3 - Good Health and Well-being ,Internal medicine ,Pancreatic cancer ,Antineoplastic Combined Chemotherapy Protocols ,medicine ,Adjuvant therapy ,Humans ,030212 general & internal medicine ,Neoadjuvant therapy ,Original Investigation ,Retrospective Studies ,Adjuvant Chemotherapy, Resected Pancreatic Cancer, Neoadjuvant FOLFIRINOX Treatment ,business.industry ,Neoadjuvant FOLFIRINOX Treatment ,Middle Aged ,medicine.disease ,Chemotherapy regimen ,Neoadjuvant Therapy ,Gemcitabine ,3. Good health ,Oxaliplatin ,Pancreatic Neoplasms ,Oncology ,Chemotherapy, Adjuvant ,030220 oncology & carcinogenesis ,Resected Pancreatic Cancer ,Fluorouracil ,business ,medicine.drug - Abstract
Importance: The benefit of adjuvant chemotherapy after resection of pancreatic cancer following neoadjuvant combination treatment with folinic acid, fluorouracil, irinotecan, and oxaliplatin (FOLFIRINOX) is unclear.Objective: To assess the association of adjuvant chemotherapy with overall survival (OS) in patients after pancreatic cancer resection and neoadjuvant FOLFIRINOX treatment.Design, Setting, and Participants: This international, multicenter, retrospective cohort study was conducted from January 1, 2012, to December 31, 2018. An existing cohort of patients undergoing resection of pancreatic cancer after FOLFIRINOX was updated and expanded for the purpose of this study. All consecutive patients who underwent pancreatic surgery after at least 2 cycles of neoadjuvant FOLFIRINOX chemotherapy for nonmetastatic pancreatic cancer were retrospectively identified from institutional databases. Patients with resectable pancreatic cancer, borderline resectable pancreatic cancer, and locally advanced pancreatic cancer were eligible for this study. Patients with in-hospital mortality or who died within 3 months after surgery were excluded.Exposures: The association of adjuvant chemotherapy with OS was evaluated in different subgroups including interaction terms for clinicopathological parameters with adjuvant treatment in a multivariable Cox model. Overall survival was defined as the time starting from surgery plus 3 months (moment eligible for adjuvant therapy), unless mentioned otherwise.Results: We included 520 patients (median [interquartile range] age, 61 [53-66] years; 279 [53.7%] men) from 31 centers in 19 countries. The median number of neoadjuvant cycles of FOLFIRINOX was 6 (interquartile range, 5-8). Overall, 343 patients (66.0%) received adjuvant chemotherapy, of whom 68 (19.8%) received FOLFIRINOX, 201 (58.6%) received gemcitabine-based chemotherapy, 14 (4.1%) received capecitabine, 45 (13.1%) received a combination or other agents, and 15 (4.4%) received an unknown type of adjuvant chemotherapy. Median OS was 38 months (95% CI, 36-46 months) after diagnosis and 31 months (95% CI, 29-37 months) after surgery. No survival difference was found for patients who received adjuvant chemotherapy vs those who did not (median OS, 29 vs 29 months, univariable hazard ratio [HR], 0.99; 95% CI, 0.77-1.28; P = .93). In multivariable analysis, only the interaction term for lymph node stage with adjuvant therapy was statistically significant: In patients with pathology-proven node-positive disease, adjuvant chemotherapy was associated with improved survival (median OS, 26 vs 13 months; multivariable HR, 0.41 [95% CI, 0.22-0.75]; P = .004). In patients with node-negative disease, adjuvant chemotherapy was not associated with improved survival (median OS, 38 vs 54 months; multivariable HR, 0.85; 95% CI, 0.35-2.10; P = .73).Conclusions and Relevance: These results suggest that adjuvant chemotherapy after neoadjuvant FOLFIRINOX and resection of pancreatic cancer was associated with improved survival only in patients with pathology-proven node-positive disease. Future randomized studies should be conducted to confirm this finding.
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- 2020
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36. Pathological Complete Response in Patients With Resected Pancreatic Adenocarcinoma After Preoperative Chemotherapy.
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Stoop TF, Oba A, Wu YHA, Beaty LE, Colborn KL, Janssen BV, Al-Musawi MH, Franco SR, Sugawara T, Franklin O, Jain A, Saiura A, Sauvanet A, Coppola A, Javed AA, Groot Koerkamp B, Miller BN, Mack CE, Hashimoto D, Caputo D, Kleive D, Sereni E, Belfiori G, Ichida H, van Dam JL, Dembinski J, Akahoshi K, Roberts KJ, Tanaka K, Labori KJ, Falconi M, House MG, Sugimoto M, Tanabe M, Gotohda N, Krohn PS, Burkhart RA, Thakkar RG, Pande R, Dokmak S, Hirano S, Burgdorf SK, Crippa S, van Roessel S, Satoi S, White SA, Hackert T, Nguyen TK, Yamamoto T, Nakamura T, Bachu V, Burns WR, Inoue Y, Takahashi Y, Ushida Y, Aslami ZV, Verbeke CS, Fariña A, He J, Wilmink JW, Messersmith W, Verheij J, Kaplan J, Schulick RD, Besselink MG, and Del Chiaro M
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- Humans, Male, Middle Aged, Female, Aged, Neoadjuvant Therapy methods, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Treatment Outcome, Cohort Studies, Oxaliplatin therapeutic use, Pancreatectomy, Pancreatic Neoplasms drug therapy, Pancreatic Neoplasms therapy, Pancreatic Neoplasms surgery, Pancreatic Neoplasms mortality, Adenocarcinoma drug therapy, Adenocarcinoma therapy, Adenocarcinoma pathology
- Abstract
Importance: Preoperative chemo(radio)therapy is increasingly used in patients with localized pancreatic adenocarcinoma, leading to pathological complete response (pCR) in a small subset of patients. However, multicenter studies with in-depth data about pCR are lacking., Objective: To investigate the incidence, outcome, and risk factors of pCR after preoperative chemo(radio)therapy., Design, Setting, and Participants: This observational, international, multicenter cohort study assessed all consecutive patients with pathology-proven localized pancreatic adenocarcinoma who underwent resection after 2 or more cycles of chemotherapy (with or without radiotherapy) in 19 centers from 8 countries (January 1, 2010, to December 31, 2018). Data collection was performed from February 1, 2020, to April 30, 2022, and analyses from January 1, 2022, to December 31, 2023. Median follow-up was 19 months., Exposures: Preoperative chemotherapy (with or without radiotherapy) followed by resection., Main Outcomes and Measures: The incidence of pCR (defined as absence of vital tumor cells in the sampled pancreas specimen after resection), its association with OS from surgery, and factors associated with pCR. Factors associated with overall survival (OS) and pCR were investigated with Cox proportional hazards and logistic regression models, respectively., Results: Overall, 1758 patients (mean [SD] age, 64 [9] years; 879 [50.0%] male) were studied. The rate of pCR was 4.8% (n = 85), and pCR was associated with OS (hazard ratio, 0.46; 95% CI, 0.26-0.83). The 1-, 3-, and 5-year OS rates were 95%, 82%, and 63% in patients with pCR vs 80%, 46%, and 30% in patients without pCR, respectively (P < .001). Factors associated with pCR included preoperative multiagent chemotherapy other than (m)FOLFIRINOX ([modified] leucovorin calcium [folinic acid], fluorouracil, irinotecan hydrochloride, and oxaliplatin) (odds ratio [OR], 0.48; 95% CI, 0.26-0.87), preoperative conventional radiotherapy (OR, 2.03; 95% CI, 1.00-4.10), preoperative stereotactic body radiotherapy (OR, 8.91; 95% CI, 4.17-19.05), radiologic response (OR, 13.00; 95% CI, 7.02-24.08), and normal(ized) serum carbohydrate antigen 19-9 after preoperative therapy (OR, 3.76; 95% CI, 1.79-7.89)., Conclusions and Relevance: This international, retrospective cohort study found that pCR occurred in 4.8% of patients with resected localized pancreatic adenocarcinoma after preoperative chemo(radio)therapy. Although pCR does not reflect cure, it is associated with improved OS, with a doubled 5-year OS of 63% compared with 30% in patients without pCR. Factors associated with pCR related to preoperative chemo(radio)therapy regimens and anatomical and biological disease response features may have implications for treatment strategies that require validation in prospective studies because they may not universally apply to all patients with pancreatic adenocarcinoma.
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- 2024
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37. Predictive value of baseline serum carbohydrate antigen 19-9 level on treatment effect of neoadjuvant chemoradiotherapy in patients with resectable and borderline resectable pancreatic cancer in two randomized trials.
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Doppenberg D, van Dam JL, Han Y, Bonsing BA, Busch OR, Festen S, van der Harst E, de Hingh IH, Homs MYV, Kwon W, Lee M, Lips DJ, de Meijer VE, Molenaar IQ, Nuyttens JJ, Patijn GA, van Roessel S, van der Schelling GP, Suker M, Versteijne E, de Vos-Geelen J, Wilmink JW, van Eijck CHJ, van Tienhoven G, Jang JY, Besselink MG, and Groot Koerkamp B
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- Humans, Neoadjuvant Therapy adverse effects, CA-19-9 Antigen therapeutic use, Randomized Controlled Trials as Topic, Carbohydrates therapeutic use, Retrospective Studies, Chemoradiotherapy, Pancreatic Neoplasms surgery, Adenocarcinoma pathology
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Background: Guidelines suggest that the serum carbohydrate antigen (CA19-9) level should be used when deciding on neoadjuvant treatment in patients with resectable and borderline resectable pancreatic ductal adenocarcinoma (hereafter referred to as pancreatic cancer). In patients with resectable pancreatic cancer, neoadjuvant therapy is advised when the CA19-9 level is 'markedly elevated'. This study investigated the impact of baseline CA19-9 concentration on the treatment effect of neoadjuvant chemoradiotherapy (CRT) in patients with resectable and borderline resectable pancreatic cancers., Methods: In this post hoc analysis, data were obtained from two RCTs that compared neoadjuvant CRT with upfront surgery in patients with resectable and borderline resectable pancreatic cancers. The effect of neoadjuvant treatment on overall survival was compared between patients with a serum CA19-9 level above or below 500 units/ml using the interaction test., Results: Of 296 patients, 179 were eligible for analysis, 90 in the neoadjuvant CRT group and 89 in the upfront surgery group. Neoadjuvant CRT was associated with superior overall survival (HR 0.67, 95 per cent c.i. 0.48 to 0.94; P = 0.019). Among 127 patients (70, 9 per cent) with a low CA19-9 level, median overall survival was 23.5 months with neoadjuvant CRT and 16.3 months with upfront surgery (HR 0.63, 0.42 to 0.93). For 52 patients (29 per cent) with a high CA19-9 level, median overall survival was 15.5 months with neoadjuvant CRT and 12.9 months with upfront surgery (HR 0.82, 0.45 to 1.49). The interaction test for CA19-9 level exceeding 500 units/ml on the treatment effect of neoadjuvant CRT was not significant (P = 0.501)., Conclusion: Baseline serum CA19-9 level defined as either high or low has prognostic value, but was not associated with the treatment effect of neoadjuvant CRT in patients with resectable and borderline resectable pancreatic cancers, in contrast with current guideline advice., (© The Author(s) 2023. Published by Oxford University Press on behalf of BJS Society Ltd.)
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- 2023
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38. Histopathological tumour response scoring in resected pancreatic cancer following neoadjuvant therapy: international interobserver study (ISGPP-1).
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Janssen BV, van Roessel S, van Dieren S, de Boer O, Adsay V, Basturk O, Brosens L, Campbell F, Chatterjee D, Chou A, Doglioni C, Esposito I, Feakins R, Fuchs TL, Fukushima N, Gill AJ, Hong SM, Hruban RH, Kaplan J, Krasinkas A, Luchini C, Shi C, Singhi A, Thompson E, Velthuysen MF, Besselink MG, Verheij J, Wang H, Verbeke C, and Fariña A
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- Humans, Eosine Yellowish-(YS), Reproducibility of Results, Observer Variation, Neoadjuvant Therapy, Pancreatic Neoplasms surgery, Pancreatic Neoplasms pathology
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Background: Most tumour response scoring systems for resected pancreatic cancer after neoadjuvant therapy score tumour regression. However, whether treatment-induced changes, including tumour regression, can be identified reliably on haematoxylin and eosin-stained slides remains unclear. Moreover, no large study of the interobserver agreement of current tumour response scoring systems for pancreatic cancer exists. This study aimed to investigate whether gastrointestinal/pancreatic pathologists can reliably identify treatment effect on tumour by histology, and to determine the interobserver agreement for current tumour response scoring systems., Methods: Overall, 23 gastrointestinal/pancreatic pathologists reviewed digital haematoxylin and eosin-stained slides of pancreatic cancer or treated tumour bed. The accuracy in identifying the treatment effect was investigated in 60 patients (30 treatment-naive, 30 after neoadjuvant therapy (NAT)). The interobserver agreement for the College of American Pathologists (CAP) and MD Anderson Cancer Center (MDACC) tumour response scoring systems was assessed in 50 patients using intraclass correlation coefficients (ICCs). An ICC value below 0.50 indicated poor reliability, 0.50 or more and less than 0.75 indicated moderate reliability, 0.75 or more and below 0.90 indicated good reliability, and above 0.90 indicated excellent reliability., Results: The sensitivity and specificity for identifying NAT effect were 76.2 and 49.0 per cent respectively. After NAT in 50 patients, ICC values for both tumour response scoring systems were moderate: 0.66 for CAP and 0.71 for MDACC., Conclusion: Identification of the effect of NAT in resected pancreatic cancer proved unreliable, and interobserver agreement for the current tumour response scoring systems was suboptimal. These findings support the recently published International Study Group of Pancreatic Pathologists recommendations to score residual tumour burden rather than tumour regression after NAT., (© The Author(s) 2022. Published by Oxford University Press on behalf of BJS Society Ltd.)
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- 2022
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39. International assessment and validation of the prognostic role of lymph node ratio in patients with resected pancreatic head ductal adenocarcinoma.
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Joliat GR, Labgaa I, Sulzer J, Vrochides D, Zerbi A, Nappo G, Perinel J, Adham M, van Roessel S, Besselink MG, Mieog JSD, Groen JV, Demartines N, and Schäfer M
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Background: Lymph node ratio (LNR; positive/harvested lymph nodes) was identified as overall survival predictor in several cancers, including pancreatic adenocarcinoma. It remains unclear if LNR is predictive of overall survival in pancreatic adenocarcinoma patients staged pN2. This study assessed the prognostic overall survival role of LNR in pancreatic adenocarcinoma patients in relation with lymph node involvement., Methods: A retrospective international study in six different centers (Europe and United States) was performed. Pancreatic adenocarcinoma patients who underwent pancreatoduodenectomy from 2000 to 2017 were included. Patients with neoadjuvant treatment, metastases, R2 resections, or missing data regarding nodal status were excluded. Survival curves were calculated using Kaplan-Meier method and compared using log-rank test. Multivariable Cox regressions were performed to find independent overall survival predictors adjusted for potential confounders., Results: A total of 1,327 patients were included. Lymph node involvement (pN+) was found in 1,026 patients (77%), 561 pN1 (55%) and 465 pN2 (45%). Median LNR in pN+ patients was 0.214 [interquartile range (IQR): 0.105-0.364]. On multivariable analysis, LNR was the strongest overall survival predictor in the entire cohort [hazard ratio (HR) =5.5; 95% confidence interval (CI): 3.1-9.9; P<0.001] and pN+ patients (HR =3.8; 95% CI: 2.2-6.6; P<0.001). Median overall survival was better in patients with LNR <0.225 compared to patients with LNR ≥0.225 in the entire cohort and pN+ patients. Similar results were found in pN2 patients (worse overall survival when LNR ≥0.225)., Conclusions: LNR appeared as an important prognostic factor in patients undergoing surgery for pancreatic adenocarcinoma and permitted to stratify overall survival in pN2 patients. LNR should be routinely used in complement to tumor-node-metastasis (TNM) stage to better predict patient prognosis., Competing Interests: Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://hbsn.amegroups.com/article/view/10.21037/hbsn-21-99/coif). The authors have no conflicts of interest to declare., (2022 Hepatobiliary Surgery and Nutrition. All rights reserved.)
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- 2022
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40. External validation of three lymph node ratio-based nomograms predicting survival using an international cohort of patients with resected pancreatic head ductal adenocarcinoma.
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Schneider M, Labgaa I, Vrochides D, Zerbi A, Nappo G, Perinel J, Adham M, van Roessel S, Besselink M, Mieog JSD, Groen JV, Demartines N, Schäfer M, and Joliat GR
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- Humans, Lymph Node Ratio, Neoplasm Staging, Nomograms, Prognosis, Carcinoma, Pancreatic Ductal pathology, Pancreatic Neoplasms pathology
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Introduction: Lymph node ratio (LNR) is an important prognostic factor of survival in patients with pancreatic ductal adenocarcinoma (PDAC). This study aimed to validate three LNR-based nomograms using an international cohort., Materials and Methods: Consecutive PDAC patients who underwent upfront pancreatoduodenectomy from six centers (Europe/USA) were collected (2000-2017). Patients with metastases, R2 resection, missing LNR data, and who died within 90 postoperative days were excluded. The updated Amsterdam nomogram, the nomogram by Pu et al., and the nomogram by Li et al. were selected. For the validation, calibration, discrimination capacity, and clinical utility were assessed., Results: After exclusion of 176 patients, 1'113 patients were included. Median overall survival (OS) of the cohort was 23 months (95% CI: 21-25). For the three nomograms, Kaplan-Meier curves showed significant OS diminution with increasing scores (p < 0.01). All nomograms showed good calibration (non-significant Hosmer-Lemeshow tests). For the Amsterdam nomogram, area under the ROC curve (AUROC) for 3-year OS was 0.64 and 0.67 for 5-year OS. Sensitivity and specificity for 3-year OS prediction were 65% and 59%. Regarding the nomogram by Pu et al., AUROC for 3- and 5-year OS were 0.66 and 0.70. Sensitivity and specificity for 3-year OS prediction were 68% and 53%. For the Li nomogram, AUROC for 3- and 5-year OS were 0.67 and 0.71, while sensitivity and specificity for 3-year OS prediction were 63% and 60%., Conclusion: The three nomograms were validated using an international cohort. Those nomograms can be used in clinical practice to evaluate survival after pancreatoduodenectomy for PDAC., (Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2022
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41. Development and external validation of a prediction model for overall survival after resection of distal cholangiocarcinoma.
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Belkouz A, Van Roessel S, Strijker M, van Dam JL, Daamen L, van der Geest LG, Balduzzi A, Cacciaguerra AB, van Dieren S, Molenaar Q, Groot Koerkamp B, Verheij J, Van Eycken E, Malleo G, Hilal MA, van Oijen MGH, Borbath I, Verslype C, Punt CJA, Besselink MG, and Klümpen HJ
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- Bile Ducts, Intrahepatic, Humans, Pancreaticoduodenectomy, Prognosis, Bile Duct Neoplasms surgery, Cholangiocarcinoma surgery
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Background: Various prognostic factors are associated with overall survival (OS) after resection of distal cholangiocarcinoma (dCCA). The objective of this study was to develop and validate a prediction model for 3-year OS after pancreatoduodenectomy for dCCA., Methods: The derivation cohort consisted of all patients who underwent pancreatoduodenectomy for dCCA in the Netherlands (2009-2016). Clinically relevant variables were selected based on the Akaike information criterion using a multivariate Cox proportional hazards regression model, with model performance being assessed by concordance index (C-index) and calibration plots. External validation was performed using patients from the Belgium Cancer Registry (2008-2016), and patients from two university hospitals of Southampton (U.K.) and Verona (Italy)., Results: Independent prognostic factors for OS in the derivation cohort of 454 patients after pancreatoduodenectomy for dCCA were age (HR 1.02, 95% CI 1.01-1.03), pT (HR 1.43, 95% CI 1.07-1.90) and pN category (pN1: HR 1.78, 95% CI 1.37-2.32; pN2: HR 2.21, 95% CI 1.63-3.01), resection margin status (HR 1.79, 95% CI 1.39-2.29) and tumour differentiation (HR 2.02, 95% CI 1.62-2.53). The prediction model was based on these prognostic factors. The optimism-adjusted C-indices were similar in the derivation cohort (0.69), and in the Belgian (0.66) and Southampton-Verona (0.68) validation cohorts. Calibration was accurate in the Belgian validation cohort (slope = 0.93, intercept = 0.12), but slightly less optimal in the Southampton-Verona validation cohort (slope = 0.88, intercept = 0.32). Based on this model, three risk groups with different prognoses were identified (3-year OS of 65.4%, 33.2% and 11.8%)., Conclusions: The prediction model for 3-year OS after resection of dCCA had reasonable performance in both the derivation and geographically external validation cohort. Calibration slightly differed between validation cohorts. The model is readily available via www. pancreascalculator.com to inform patients from Western European countries on their prognosis, and may be used to stratify patients for clinical trials., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)
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- 2022
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42. International Validation of a Nomogram to Predict Recurrence after Resection of Grade 1 and 2 Nonfunctioning Pancreatic Neuroendocrine Tumors.
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Heidsma CM, van Roessel S, van Dieren S, Engelsman AF, Strobel O, Buechler MW, Schimmack S, Perinel J, Adham M, Deshpande V, Kjaer J, Norlen O, Gill AJ, Samra JS, Mittal A, Hoogwater FJH, Primavesi F, Stättner S, Besselink MG, van Eijck CHJ, and Nieveen van Dijkum EJM
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- Humans, Nomograms, Prognosis, Retrospective Studies, Neuroectodermal Tumors, Primitive, Neuroendocrine Tumors diagnosis, Neuroendocrine Tumors pathology, Neuroendocrine Tumors surgery, Pancreatic Neoplasms pathology
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Background: Despite the low recurrence rate of resected nonfunctional pancreatic neuroendocrine tumors (NF-pNETs), nearly all patients undergo long-term surveillance. A prediction model for recurrence may help select patients for less intensive surveillance or identify patients for adjuvant therapy. The objective of this study was to assess the external validity of a recently published model predicting recurrence within 5 years after surgery for NF-pNET in an international cohort. This prediction model includes tumor grade, lymph node status and perineural invasion as predictors., Methods: Retrospectively, data were collected from 7 international referral centers on patients who underwent resection for a grade 1-2 NF-pNET between 1992 and 2018. Model performance was evaluated by calibration statistics, Harrel's C-statistic, and area under the curve (AUC) of the receiver operating characteristic curve for 5-year recurrence-free survival (RFS). A sub-analysis was performed in pNETs >2 cm. The model was improved to stratify patients into 3 risk groups (low, medium, high) for recurrence., Results: Overall, 342 patients were included in the validation cohort with a 5-year RFS of 83% (95% confidence interval [CI]: 78-88%). Fifty-eight patients (17%) developed a recurrence. Calibration showed an intercept of 0 and a slope of 0.74. The C-statistic was 0.77 (95% CI: 0.70-0.83), and the AUC for the prediction of 5-year RFS was 0.74. The prediction model had a better performance in tumors >2 cm (C-statistic 0.80)., Conclusions: External validity of this prediction model for recurrence after curative surgery for grade 1-2 NF-pNET showed accurate overall performance using 3 easily accessible parameters. This model is available via www.pancreascalculator.com., (© 2021 The Author(s) Published by S. Karger AG, Basel.)
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- 2022
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43. Venous wedge and segment resection during pancreatoduodenectomy for pancreatic cancer: impact on short- and long-term outcomes in a nationwide cohort analysis.
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Groen JV, Michiels N, van Roessel S, Besselink MG, Bosscha K, Busch OR, van Dam R, van Eijck CHJ, Koerkamp BG, van der Harst E, de Hingh IH, Karsten TM, Lips DJ, de Meijer VE, Molenaar IQ, Nieuwenhuijs VB, Roos D, van Santvoort HC, Wijsman JH, Wit F, Zonderhuis BM, de Vos-Geelen J, Wasser MN, Bonsing BA, Stommel MWJ, and Mieog JSD
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- Aged, Female, Humans, Male, Middle Aged, Pancreas surgery, Pancreaticoduodenectomy adverse effects, Pancreaticoduodenectomy mortality, Retrospective Studies, Survival Analysis, Treatment Outcome, Mesenteric Veins surgery, Pancreatic Neoplasms surgery, Pancreaticoduodenectomy methods, Portal Vein surgery
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Background: Venous resection of the superior mesenteric or portal vein is increasingly performed in pancreatic cancer surgery, whereas results of studies on short- and long-term outcomes are contradictory. The aim of this study was to evaluate the impact of the type of venous resection in pancreatoduodenectomy for pancreatic cancer on postoperative morbidity and overall survival., Methods: This nationwide retrospective cohort study included all patients who underwent pancreatoduodenectomy for pancreatic cancer in 18 centres (2013-2017)., Results: A total of 1311 patients were included, of whom 17 per cent underwent wedge resection and 10 per cent segmental resection. Patients with segmental resection had higher rates of major morbidity (39 versus 20 versus 23 per cent, respectively; P < 0.001) and portal or superior mesenteric vein thrombosis (18 versus 5 versus 1 per cent, respectively; P < 0.001) and worse overall survival (median 12 versus 16 versus 20 months, respectively; P < 0.001), compared to patients with wedge resection and those without venous resection. Multivariable analysis showed patients with segmental resection, but not those who had wedge resection, had higher rates of major morbidity (odds ratio = 1.93, 95 per cent c.i. 1.20 to 3.11) and worse overall survival (hazard ratio = 1.40, 95 per cent c.i. 1.10 to 1.78), compared to patients without venous resection. Among patients who received neoadjuvant therapy, there was no difference in overall survival among patients with segmental and wedge resection and those without venous resection (median 32 versus 25 versus 33 months, respectively; P = 0.470), although there was a difference in major morbidity rates (52 versus 19 versus 21 per cent, respectively; P = 0.012)., Conclusion: In pancreatic surgery, the short- and long-term outcomes are worse in patients with venous segmental resection, compared to patients with wedge resection and those without venous resection., (© The Author(s) 2021. Published by Oxford University Press on behalf of BJS Society Ltd.)
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- 2021
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44. Artificial Intelligence-Based Segmentation of Residual Tumor in Histopathology of Pancreatic Cancer after Neoadjuvant Treatment.
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Janssen BV, Theijse R, van Roessel S, de Ruiter R, Berkel A, Huiskens J, Busch OR, Wilmink JW, Kazemier G, Valkema P, Farina A, Verheij J, de Boer OJ, and Besselink MG
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Background: Histologic examination of resected pancreatic cancer after neoadjuvant therapy (NAT) is used to assess the effect of NAT and may guide the choice for adjuvant treatment. However, evaluating residual tumor burden in pancreatic cancer is challenging given tumor response heterogeneity and challenging histomorphology. Artificial intelligence techniques may offer a more reproducible approach., Methods: From 64 patients, one H&E-stained slide of resected pancreatic cancer after NAT was digitized. Three separate classes were manually outlined in each slide (i.e., tumor, normal ducts, and remaining epithelium). Corresponding segmentation masks and patches were generated and distributed over training, validation, and test sets. Modified U-nets with varying encoders were trained, and F1 scores were obtained to express segmentation accuracy., Results: The highest mean segmentation accuracy was obtained using modified U-nets with a DenseNet161 encoder. Tumor tissue was segmented with a high mean F1 score of 0.86, while the overall multiclass average F1 score was 0.82., Conclusions: This study shows that artificial intelligence-based assessment of residual tumor burden is feasible given the promising obtained F1 scores for tumor segmentation. This model could be developed into a tool for the objective evaluation of the response to NAT and may potentially guide the choice for adjuvant treatment.
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- 2021
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45. Preoperative misdiagnosis of pancreatic and periampullary cancer in patients undergoing pancreatoduodenectomy: A multicentre retrospective cohort study.
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van Roessel S, Soer EC, Daamen LA, van Dalen D, Fariña Sarasqueta A, Stommel MWJ, Molenaar IQ, van Santvoort HC, van de Vlasakker VCJ, de Hingh IHJT, Groen JV, Mieog JSD, van Dam JL, van Eijck CHJ, van Tienhoven G, Klümpen HJ, Wilmink JW, Busch OR, Brosens LAA, Groot Koerkamp B, Verheij J, and Besselink MG
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- Aged, Ampulla of Vater, Blood Vessels diagnostic imaging, Cholangiocarcinoma surgery, Common Bile Duct Neoplasms surgery, Duodenal Neoplasms surgery, Endoscopic Ultrasound-Guided Fine Needle Aspiration, Female, Humans, Male, Middle Aged, Pancreas blood supply, Pancreatic Neoplasms diagnostic imaging, Pancreatic Neoplasms surgery, Pancreaticoduodenectomy, Predictive Value of Tests, Preoperative Period, Retrospective Studies, Survival Rate, Tumor Burden, Cholangiocarcinoma diagnosis, Common Bile Duct Neoplasms diagnosis, Diagnostic Errors statistics & numerical data, Duodenal Neoplasms diagnosis, Pancreatic Neoplasms diagnosis, Pancreatic Neoplasms pathology
- Abstract
Introduction: Whereas neoadjuvant chemo(radio)therapy is increasingly used in pancreatic cancer, it is currently not recommended for other periampullary (non-pancreatic) cancers. This has important implications for the relevance of the preoperative diagnosis for pancreatoduodenectomy. This retrospective multicentre cohort study aimed to determine the frequency of clinically relevant misdiagnoses in patients undergoing pancreatoduodenectomy for pancreatic or other periampullary cancer., Methods: Data from all consecutive patients who underwent a pancreatoduodenectomy between 2014 and 2018 were obtained from the prospective Dutch Pancreatic Cancer Audit. The preoperative diagnosis as concluded by the multidisciplinary team (MDT) meeting was compared with the final postoperative diagnosis at pathology to determine the rate of clinically relevant misdiagnosis (defined as missed pancreatic cancer or incorrect diagnosis of pancreatic cancer)., Results: In total, 1244 patients underwent pancreatoduodenectomy of whom 203 (16%) had a clinically relevant misdiagnosis preoperatively. Of all patients with a final diagnosis of pancreatic cancer, 13% (87/679) were preoperatively misdiagnosed as distal cholangiocarcinoma (n = 41, 6.0%), ampullary cancer (n = 27, 4.0%) duodenal cancer (n = 16, 2.4%), or other (n = 3, 0.4%). Of all patients with a final diagnosis of periampullary (non-pancreatic) cancer, 21% (116/565) were preoperatively incorrectly diagnosed as pancreatic cancer. Accuracy of preoperative diagnosis was 84% for pancreatic cancer, 71% for distal cholangiocarcinoma, 73% for ampullary cancer and 73% for duodenal cancer. A prediction model for the preoperative likelihood of pancreatic cancer (versus other periampullary cancer) prior to pancreatoduodenectomy demonstrated an AUC of 0.88., Discussion: This retrospective multicentre cohort study showed that 16% of patients have a clinically relevant misdiagnosis that could result in either missing the opportunity of neoadjuvant chemotherapy in patients with pancreatic cancer or inappropriate administration of neoadjuvant chemotherapy in patients with non-pancreatic periampullary cancer. A preoperative prediction model is available on www.pancreascalculator.com., 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 © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2021
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46. Resection of the Portal-Superior Mesenteric Vein in Pancreatic Cancer: Pathological Assessment and Recurrence Patterns.
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Groen JV, van Manen L, van Roessel S, van Dam JL, Bonsing BA, Doukas M, van Eijck CHJ, Farina Sarasqueta A, Putter H, Vahrmeijer AL, Verheij J, Besselink MG, Groot Koerkamp B, and Mieog JSD
- Subjects
- Aged, Female, Humans, Male, Mesenteric Veins pathology, Middle Aged, Neoplasm Invasiveness pathology, Neoplasm Recurrence, Local, Neoplasm Staging, Pancreatic Neoplasms mortality, Pancreatic Neoplasms pathology, Pancreaticoduodenectomy, Portal Vein pathology, Retrospective Studies, Survival Rate, Mesenteric Veins surgery, Pancreatic Neoplasms surgery, Portal Vein surgery
- Abstract
Objectives: The portal vein (PV)-superior mesenteric vein (SMV) margin is the most affected margin in pancreatic cancer. This study investigates the association between venous resection, tumor invasion in the resected PV-SMV, recurrence patterns, and overall survival (OS)., Methods: This multicenter cohort study included patients who underwent pancreatoduodenectomy for pancreatic cancer (2010-2017). In addition, a systematic literature search was performed., Results: In total, 531 patients were included, of which 149 (28%) underwent venous resection of whom 53% had tumor invasion in the resected PV-SMV. Patients with venous resection had a significant higher rate of R1 margins (69% vs 37%) and had more often multiple R1 margins (43% vs 16%). Patient with venous resection had a significant shorter time to locoregional recurrence and a shorter OS (15 vs 19 months). At multivariable analyses, venous resection and tumor invasion in the resected PV-SMV were not predictive for time to recurrence and OS. The literature overview showed that pathological assessment of the resected PV-SMV is not adequately standardized., Conclusions: Only half of patients with venous resection had pathology confirmed tumor invasion in the resected PV-SMV, and both are not independently associated with time to recurrence and OS. The pathological assessment of the resected PV-SMV needs to be standardized., Competing Interests: The authors declare no conflict of interest., (Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.)
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- 2021
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47. Axial slicing versus bivalving in the pathological examination of pancreatoduodenectomy specimens (APOLLO): a multicentre randomized controlled trial.
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van Roessel S, Soer EC, van Dieren S, Koens L, van Velthuysen MLF, Doukas M, Groot Koerkamp B, Fariña Sarasqueta A, Bronkhorst CM, Raicu GM, Kuijpers KC, Seldenrijk CA, van Santvoort HC, Molenaar IQ, van der Post RS, Stommel MWJ, Busch OR, Besselink MG, Brosens LAA, and Verheij J
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- Humans, Pancreaticoduodenectomy adverse effects, Ampulla of Vater surgery, Common Bile Duct Neoplasms surgery, Duodenal Neoplasms, Pancreatic Neoplasms surgery
- Abstract
Background: In pancreatoduodenectomy specimens, dissection method may affect the assessment of primary tumour origin (i.e. pancreatic, distal bile duct or ampullary adenocarcinoma), which is primarily determined macroscopically. This is the first study to prospectively compare the two commonly used techniques, i.e. axial slicing and bivalving., Methods: In four centres, a randomized controlled trial was performed in specimens of patients with a suspected (pre)malignant tumour in the pancreatic head. Primary outcome measure was the level of certainty (scale 0-100) regarding tumour origin by four independent gastrointestinal pathologists based on macroscopic assessment. Secondary outcomes were inter-observer agreement and R1 rate., Results: In total, 128 pancreatoduodenectomy specimens were randomized. The level of certainty in determining the primary tumour origin did not differ between axial slicing and bivalving (mean score 72 [sd 13] vs. 68 [sd 16], p = 0.21), nor did inter-observer agreement, both being moderate (kappa 0.45 vs. 0.47). In pancreatic cancer specimens, R1 rate (60% vs. 55%, p = 0.71) and the number of harvested lymph nodes (median 16 vs. 17, p = 0.58) were similar., Conclusion: This study demonstrated no differences in determining the tumour origin between axial slicing and bivalving. Both techniques performed similarly regarding inter-observer agreement, R1 rate, and lymph node harvest., (Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
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- 2021
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48. Predicting overall survival and resection in patients with locally advanced pancreatic cancer treated with FOLFIRINOX: Development and internal validation of two nomograms.
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Brada LJH, Walma MS, Daamen LA, van Roessel S, van Dam RM, de Hingh IH, Liem MLS, de Meijer VE, Patijn GA, Festen S, Stommel MWJ, Bosscha K, Polée MB, Yung Nio C, Wessels FJ, de Vries JJJ, van Lienden KP, Bruijnen RC, Los M, Mohammad NH, Wilmink HW, Busch OR, Besselink MG, Quintus Molenaar I, and van Santvoort HC
- Subjects
- Adenocarcinoma pathology, Adenocarcinoma therapy, Aged, Combined Modality Therapy, Female, Fluorouracil therapeutic use, Follow-Up Studies, Humans, Irinotecan therapeutic use, Leucovorin therapeutic use, Male, Middle Aged, Oxaliplatin therapeutic use, Pancreatic Neoplasms pathology, Pancreatic Neoplasms therapy, Prognosis, Prospective Studies, Survival Rate, Adenocarcinoma mortality, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Nomograms, Pancreatectomy mortality, Pancreatic Neoplasms mortality
- Abstract
Background and Objectives: Patients with locally advanced pancreatic cancer (LAPC) are increasingly treated with FOLFIRINOX, resulting in improved survival and resection of tumors that were initially unresectable. It remains unclear, however, which specific patients benefit from FOLFIRINOX. Two nomograms were developed predicting overall survival (OS) and resection at the start of FOLFIRINOX for LAPC., Methods: From our multicenter, prospective LAPC registry in 14 Dutch hospitals, LAPC patients starting first-line FOLFIRINOX (April 2015-December 2017) were included. Stepwise backward selection according to the Akaike Information Criterion was used to identify independent baseline predictors for OS and resection. Two prognostic nomograms were generated., Results: A total of 252 patients were included, with a median OS of 14 months. Thirty-two patients (13%) underwent resection, with a median OS of 23 months. Older age, female sex, Charlson Comorbidity Index ≤1, and CA 19.9 < 274 were independent factors predicting a better OS (c-index: 0.61). WHO ps >1, involvement of the superior mesenteric artery, celiac trunk, and superior mesenteric vein ≥ 270° were independent factors decreasing the probability of resection (c-index: 0.79)., Conclusions: Two nomograms were developed to predict OS and resection in patients with LAPC before starting treatment with FOLFIRINOX. These nomograms could be beneficial in the shared decision-making process and counseling of these patients., (© 2021 Wiley Periodicals LLC.)
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- 2021
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49. Using Textbook Outcomes to benchmark practice in pancreatic surgery.
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Nicholas E, van Roessel S, de Burlet K, Hore T, Besselink MG, and Connor S
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- Female, Humans, Male, Middle Aged, Netherlands epidemiology, Pancreatectomy, Pancreaticoduodenectomy, Retrospective Studies, Treatment Outcome, Benchmarking, Pancreatic Neoplasms surgery
- Abstract
Background: Textbook Outcome (TO) is a novel composite measure of clinical outcomes that can be used to measure the quality of surgical outcomes. TOs for pancreatic surgery were published by the Dutch Pancreatic Cancer Group (DPCG) in 2020. The aim of this study was to explore how a medium volume hepatopancreaticobiliary unit could use TO to benchmark local outcomes following pancreatic surgery., Methods: Retrospective analysis of prospectively collected data from patients who underwent pancreaticoduodenectomy (PD) or distal pancreatectomy (DP) for all indications between March 2005 and February 2020 at Christchurch Hospital (CH). Analysis of TO items as defined by the DPCG was performed and compared to nationwide Dutch outcomes (2014-2017), including cumulative analysis using CuSum., Results: In total, 273 patients were included (median age 63 years; 51% female) of which 182 (67%) underwent PD and 91 (33%) underwent DP (median annual volume 12 PDs/6 DPs). Overall, 58% of patients undergoing PD and 74% of patients undergoing DP achieved TO, compared with 58% and 67%, P = 0.944 and P = 0.231, respectively, for the Netherlands (median annual volume 33 PDs/8 DPs per hospital)., Conclusions: TO offers a useful quality measure to benchmark local outcomes following pancreatic surgery against an external nationwide analysis. The results show that as a medium volume centre performance was comparable to previously published Dutch results, which included high volume centres. Applying CuSum methodology to the TO metric allows a continuous measure of performance. This offers the potential to provide feedback for quality improvement strategies., (© 2021 Royal Australasian College of Surgeons.)
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- 2021
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50. Microscopic resection margin status in pancreatic ductal adenocarcinoma - A nationwide analysis.
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Daamen LA, van Goor IWJM, Schouten TJ, Dorland G, van Roessel SR, Besselink MG, Bonsing BA, Bosscha K, Brosens LAA, Busch OR, van Dam RM, Fariña Sarasqueta A, Festen S, Groot Koerkamp B, van der Harst E, de Hingh IHJT, Intven MPW, Kazemier G, de Meijer VE, Nieuwenhuijs VB, Raicu GM, Roos D, Schreinemakers JMJ, Stommel MWJ, van Velthuysen MF, Verheij J, Verkooijen HM, van Santvoort HC, and Molenaar IQ
- Subjects
- Aged, Carcinoma, Pancreatic Ductal pathology, Cohort Studies, Disease-Free Survival, Female, Humans, Logistic Models, Male, Middle Aged, Multivariate Analysis, Netherlands, Pancreatic Neoplasms pathology, Prognosis, Proportional Hazards Models, Survival Rate, Carcinoma, Pancreatic Ductal surgery, Margins of Excision, Pancreatic Neoplasms surgery
- Abstract
Introduction: First, this study aimed to assess the prognostic value of different definitions for resection margin status on disease-free survival (DFS) and overall survival (OS) in pancreatic ductal adenocarcinoma (PDAC). Second, preoperative predictors of direct margin involvement were identified., Materials and Methods: This nationwide observational cohort study included all patients who underwent upfront PDAC resection (2014-2016), as registered in the prospective Dutch Pancreatic Cancer Audit. Patients were subdivided into three groups: R0 (≥1 mm margin clearance), R1 (<1 mm margin clearance) or R1 (direct margin involvement). Survival was compared using multivariable Cox regression analysis. Logistic regression with baseline variables was performed to identify preoperative predictors of R1 (direct)., Results: 595 patients with a median OS of 18 months (IQR 10-32 months) months were analysed. R0 (≥1 mm) was achieved in 277 patients (47%), R1 (<1 mm) in 146 patients (24%) and R1 (direct) in 172 patients (29%). R1 (direct) was associated with a worse OS, as compared with both R0 (≥1 mm) (hazard ratio (HR) 1.35 [95% and confidence interval (CI) 1.08-1.70); P < 0.01) and R1 (<1 mm) (HR 1.29 [95%CI 1.01-1.67]; P < 0.05). No OS difference was found between R0 (≥1 mm) and R1 (<1 mm) (HR 1.05 [95% CI 0.82-1.34]; P = 0.71). Preoperative predictors associated with an increased risk of R1 (direct) included age, male sex, performance score 2-4, and venous or arterial tumour involvement., Conclusion: Resection margin clearance of <1 mm, but without direct margin involvement, does not affect survival, as compared with a margin clearance of ≥1 mm. Given that any vascular tumour involvement on preoperative imaging was associated with an increased risk of R1 (direct) resection with upfront surgery, neoadjuvant therapy might be considered in these patients., Competing Interests: Declaration of competing interest The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article., (Copyright © 2020. Published by Elsevier Ltd.)
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- 2021
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