TY - JOUR
T1 - Preoperative radiotherapy plus surgery versus surgery alone for patients with primary retroperitoneal sarcoma (EORTC-62092
T2 - STRASS): a multicentre, open-label, randomised, phase 3 trial
AU - Bonvalot, Sylvie
AU - Gronchi, Alessandro
AU - Le Péchoux, Cécile
AU - Swallow, Carol J.
AU - Strauss, Dirk
AU - Meeus, Pierre
AU - van Coevorden, Frits
AU - Stoldt, Stephan
AU - Stoeckle, Eberhard
AU - Rutkowski, Piotr
AU - Rastrelli, Marco
AU - Raut, Chandrajit P.
AU - Hompes, Daphne
AU - De Paoli, Antonino
AU - Sangalli, Claudia
AU - Honoré, Charles
AU - Chung, Peter
AU - Miah, Aisha
AU - Blay, Jean Yves
AU - Fiore, Marco
AU - Stelmes, Jean Jacques
AU - Dei Tos, Angelo P.
AU - Baldini, Elizabeth H.
AU - Litière, Saskia
AU - Marreaud, Sandrine
AU - Gelderblom, Hans
AU - Haas, Rick L.
N1 - Funding Information:
SB reports personal fees and non-financial support from Nanobiotix and PharmaMar, and non-financial support from Pfizer, outside the submitted work. AG reports personal fees from Novartis, Pfizer, Bayer, Lilly Oncology, SpringWorks, and Nanobiotix, and grants and personal fees from PharmaMar, all outside the submitted work. CLP reports personal fees from AstraZeneca, Amgen, Nanobiotix, Roche, Medscape, PrimeOncology, and Lilly, outside the submitted work. PR reports personal fees from Novartis, Merck Sharp & Dohme, Bristol-Myers Squibb, Roche, Pfizer, Blueprint Medicines, Pierre Fabre, and Sanofi, outside the submitted work. PC reports personal fees from AbbVie and AstraZeneca, outside the submitted work. AM reports grants from National Health Service (NHS) funding to the National Institute for Health Research Biomedical Research Centre for Cancer at The Royal Marsden Hospital and The Institute of Cancer Research, during the conduct of the study. JYB reports grants from European Clinical Trials in Rare Sarcomas (EUROSARC), Lyon Integrative Cancer Research Program (LYRICAN), the European Network for Rare Adult Solid Cancers (EURACAN), NetSarc+, and Intersarc, during the conduct of the study. APDT reports personal fees from Roche, PharmaMar, and Bayer, outside the submitted work. All other authors declare no competing interests.
Funding Information:
The research leading to these results has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant 278742 (EUROSARC) to JYB and a grant from the European Organisation for Research and Treatment of Cancer (EORTC). We thank Axelle Nzokirantevye, Facundo Zaffaroni, Sandrine Rivrain, Lucia Senna, Ionela Stanciu, Stéphanie Kromar, and the other staff at the EORTC headquarters who contributed to the success of the trial. We thank Nicolas Penel (Centre Oscar Lambret Lille, France) who helped us to write the protocol. We are grateful to all the patients who took part, and their relatives. We thank the participating investigators and centres who worked on the study: A Krarup-Hansen (Herlev Hospital, University Copenhagen, Copenhagen, Denmark), J Sherriff (University Hospitals Birmingham Queen Elizabeth Medical Centre, Birmingham, UK), R-J van Ginkel (University Medical Center Groningen, Groningen, the Netherlands), ADG Krol (Leiden University Medical Centre, Leiden, the Netherlands), V Quagliuolo (Istituto Clinico Humanitas, Rozzano, Italy), H Bonenkamp (Radboud University Medical Center Nijmegen, Nijmegen, the Netherlands), M Beasley (University Hospitals Bristol NHS Foundation, Bristol Haematology and Oncology Centre, Bristol, UK), P Wilson (University Hospitals Bristol NHS Foundation, Bristol Haematology and Oncology Centre, Bristol, UK), M Hatton (Sheffield Teaching Hospitals NHS Foundation, Weston Park Hospital, Sheffield, UK), J Wylie (The Christie NHS Foundation Trust, Manchester, UK), D Van Gestel (Institut Jules Bordet, Hopital Universitaire University Libres Brussels, Brussels, Belgium), A Casado Herraez (Hospital Universitario San Carlos, Madrid, Spain), C Valverde (Vall d'Hebron Institut Oncologia, Barcelona, Spain), A Ducassou (Institut Claudius Regaud, Toulouse, France), J Theisen (Technische Unversität München, Munich, Germany), P Hohenberger (Universitaets Medizin Mannheim, Mannheim, Germany), S Helfre (Institut Curie; Paris, France), P Wong (Centre Hospitalier de l'Université de Montreal, Montreal, Canada), F Colin and C Charon Barra (Histopathology Department, Centre de Lutte Contre le Cancer Georges-François Leclerc, Dijon, France), J Ahlen (Karolinska University Hospital, Stockholm, Sweden), G Ayre (University Hospitals Bristol NHS Foundation, Bristol Haematology and Oncology Centre, Bristol, UK), J Bovée (Department of Pathology, Leiden University Medical Center, Leiden, Netherlands), E Wardelmann (Gerhard Domagk Institute of Pathology, University Hospital Münster, Germany), K Thway (Histopathology Department, The Royal Marsden NHS Foundation Trust, London, UK), and C Fisher (Histopathology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham UK).
Publisher Copyright:
© 2020 Elsevier Ltd
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/10
Y1 - 2020/10
N2 - Background: Unlike for extremity sarcomas, the efficacy of radiotherapy for retroperitoneal sarcoma is not established. The aim of this study was to evaluate the impact of preoperative radiotherapy plus surgery versus surgery alone on abdominal recurrence-free survival. Methods: EORTC-62092 is an open-label, randomised, phase 3 study done in 31 research institutions, hospitals, and cancer centres in 13 countries in Europe and North America. Adults (aged ≥18 years) with histologically documented, localised, primary retroperitoneal sarcoma that was operable and suitable for radiotherapy, who had not been previously treated and had a WHO performance status and American Society of Anesthesiologists score of 2 or lower, were centrally randomly assigned (1:1), using an interactive web response system and a minimisation algorithm, to receive either surgery alone or preoperative radiotherapy followed by surgery. Randomisation was stratified by hospital and performance status. Radiotherapy was delivered as 50·4 Gy (in 28 daily fractions of 1·8 Gy) in either 3D conformal radiotherapy or intensity modulated radiotherapy, and the objective of surgery was a macroscopically complete resection of the tumour mass with en-bloc organ resection as necessary. The primary endpoint was abdominal recurrence-free survival, as assessed by the investigator, and was analysed in the intention-to-treat population. Safety was analysed in all patients who started their allocated treatment. This trial is registered with ClinicalTrials.gov, NCT01344018. Findings: Between Jan 18, 2012 and April 10, 2017, 266 patients were enrolled, of whom 133 were randomly assigned to each group. The median follow-up was 43·1 months (IQR 28·8–59·2). 128 (96%) patients from the surgery alone group had surgery, and 119 (89%) patients in the radiotherapy and surgery group had both radiotherapy and surgery. Median abdominal recurrence-free survival was 4·5 years (95% CI 3·9 to not estimable) in the radiotherapy plus surgery group and 5·0 years (3·4 to not estimable) in the surgery only group (hazard ratio 1·01, 95% CI 0·71–1·44; log rank p=0·95). The most common grade 3–4 adverse events were lymphopenia (98 [77%] of 127 patients in the radiotherapy plus surgery group vs one [1%] of 128 patients in the surgery alone group), anaemia (15 [12%] vs ten [8%]), and hypoalbuminaemia (15 [12%] vs five [4%]). Serious adverse events were reported in 30 (24%) of 127 patients in the radiotherapy plus surgery group, and in 13 (10%) of 128 patients in the surgery alone group. One (1%) of 127 patients in the radiotherapy plus surgery group died due to treatment-related serious adverse events (gastropleural fistula), and no patients in the surgery alone group died due to treatment-related serious adverse events. Interpretation: Preoperative radiotherapy should not be considered as standard of care treatment for retroperitoneal sarcoma. Funding: European Organisation for Research and Treatment of Cancer, and European Clinical Trials in Rare Sarcomas.
AB - Background: Unlike for extremity sarcomas, the efficacy of radiotherapy for retroperitoneal sarcoma is not established. The aim of this study was to evaluate the impact of preoperative radiotherapy plus surgery versus surgery alone on abdominal recurrence-free survival. Methods: EORTC-62092 is an open-label, randomised, phase 3 study done in 31 research institutions, hospitals, and cancer centres in 13 countries in Europe and North America. Adults (aged ≥18 years) with histologically documented, localised, primary retroperitoneal sarcoma that was operable and suitable for radiotherapy, who had not been previously treated and had a WHO performance status and American Society of Anesthesiologists score of 2 or lower, were centrally randomly assigned (1:1), using an interactive web response system and a minimisation algorithm, to receive either surgery alone or preoperative radiotherapy followed by surgery. Randomisation was stratified by hospital and performance status. Radiotherapy was delivered as 50·4 Gy (in 28 daily fractions of 1·8 Gy) in either 3D conformal radiotherapy or intensity modulated radiotherapy, and the objective of surgery was a macroscopically complete resection of the tumour mass with en-bloc organ resection as necessary. The primary endpoint was abdominal recurrence-free survival, as assessed by the investigator, and was analysed in the intention-to-treat population. Safety was analysed in all patients who started their allocated treatment. This trial is registered with ClinicalTrials.gov, NCT01344018. Findings: Between Jan 18, 2012 and April 10, 2017, 266 patients were enrolled, of whom 133 were randomly assigned to each group. The median follow-up was 43·1 months (IQR 28·8–59·2). 128 (96%) patients from the surgery alone group had surgery, and 119 (89%) patients in the radiotherapy and surgery group had both radiotherapy and surgery. Median abdominal recurrence-free survival was 4·5 years (95% CI 3·9 to not estimable) in the radiotherapy plus surgery group and 5·0 years (3·4 to not estimable) in the surgery only group (hazard ratio 1·01, 95% CI 0·71–1·44; log rank p=0·95). The most common grade 3–4 adverse events were lymphopenia (98 [77%] of 127 patients in the radiotherapy plus surgery group vs one [1%] of 128 patients in the surgery alone group), anaemia (15 [12%] vs ten [8%]), and hypoalbuminaemia (15 [12%] vs five [4%]). Serious adverse events were reported in 30 (24%) of 127 patients in the radiotherapy plus surgery group, and in 13 (10%) of 128 patients in the surgery alone group. One (1%) of 127 patients in the radiotherapy plus surgery group died due to treatment-related serious adverse events (gastropleural fistula), and no patients in the surgery alone group died due to treatment-related serious adverse events. Interpretation: Preoperative radiotherapy should not be considered as standard of care treatment for retroperitoneal sarcoma. Funding: European Organisation for Research and Treatment of Cancer, and European Clinical Trials in Rare Sarcomas.
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U2 - 10.1016/S1470-2045(20)30446-0
DO - 10.1016/S1470-2045(20)30446-0
M3 - Article
VL - 21
SP - 1366
EP - 1377
JO - The Lancet Oncology
JF - The Lancet Oncology
SN - 1470-2045
IS - 10
ER -