TY - JOUR
T1 - Guidelines for time-to-event end-point definitions in adjuvant randomised trials for patients with localised colon cancer
T2 - Results of the DATECAN initiative
AU - ACCENT Group
AU - Cohen, Romain
AU - Vernerey, Dewi
AU - Bellera, Carine
AU - Meurisse, Aurélia
AU - Henriques, Julie
AU - Paoletti, Xavier
AU - Rousseau, Benoît
AU - Alberts, Steven
AU - Aparicio, Thomas
AU - Boukovinas, Ioannis
AU - Gill, Sharlene
AU - Goldberg, Richard M.
AU - Grothey, Axel
AU - Hamaguchi, Tetsuya
AU - Iveson, Timothy
AU - Kerr, Rachel
AU - Labianca, Roberto
AU - Lonardi, Sara
AU - Meyerhardt, Jeffrey
AU - Paul, James
AU - Punt, Cornelis J.A.
AU - Saltz, Leonard
AU - Saunders, Marck P.
AU - Schmoll, Hans Joachim
AU - Shah, Manish
AU - Sobrero, Alberto
AU - Souglakos, Ioannis
AU - Taieb, Julien
AU - Takashima, Atsuo
AU - Wagner, Anna Dorothea
AU - Ychou, Marc
AU - Bonnetain, Franck
AU - Gourgou, Sophie
AU - Yoshino, Takayuki
AU - Yothers, Greg
AU - de Gramont, Aimery
AU - Shi, Qian
AU - André, Thierry
N1 - Funding Information:
This work was supported by the A.R.C.A.D (Aide et Recherche en Cancérologie Digestive) foundation.
Funding Information:
L.S. has received research funds from Taiho Pharmaceutical. M.S. has received honoraria for meetings/lectures from Roche, Merck, Sanofi, Servier and Amgen. R.C. has received honoraria from Amgen, Sanofi and Servier and travel fees from Sanofi. T.A. has served in a consulting/advisory role, and/or received honoraria from Amgen, Bristol-Myers Squibb, Chugai, HalioDx, MSD Oncology, Pierre Fabre, Roche/Ventana, Sanofi and Servier and has received travel accommodations and expenses from Roche/Genentech, MSD Oncology and Bristol-Myers Squibb. T.Y. has received funding from Novartis Pharma K.K., MSD K.K., Sumitomo Dainippon Pharma Co., Ltd., Chugai Pharmaceutical Co. Ltd., Sanofi K.K., Daiichi Sankyo Co. Ltd., PAREXEL International Inc. and Ono Pharmaceutical Co. Ltd. ADW reports personal fees from Bristol-Myers Squibb, Servier Suisse, Merck, Merck Sharp & Dohme, Bayer, EMD Serono, Lilly, Sanofi, and Celgene, non-financial support from AstraZeneca, AbbVie, Sanofi-Adventis Deutchland, SHIRE, and PFIZER. All remaining authors have declared no conflicts of interest.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/5
Y1 - 2020/5
N2 - Background: The variability of definitions for time-to-event (TTE) end-points impacts the conclusions of randomised clinical trials (RCTs). The Definition for the Assessment of Time-to-event Endpoints in CANcer (DATECAN) initiative aims to provide consensus definitions for TTE end-points used in RCTs. Here, we formulate guidelines for adjuvant colon cancer RCTs. Methods: We performed a literature review to identify TTE end-points and events included in their definition in RCT publications. Then, a consensus was reached among a panel of international experts, using a formal modified Delphi method, with 2 rounds of questionnaires and an in-person meeting. Results: Twenty-four experts scored 72 events involved in 6 TTE end-points. Consensus was reached for 24%, 57% and 100% events after the first round, second round and in-person meeting. For RCTs not using overall survival as their primary end-point, the experts recommend using disease-free survival (DFS) rather than recurrence-free survival (RFS) or time to recurrence (TTR) as the primary end-point. The consensus definition of DFS includes all causes of death, second primary colorectal cancers (CRCs), anastomotic relapse and metastatic relapse as an event, but not second primary non-CRCs. Events included in the RFS definition are the same as for DFS with the exception of second primary CRCs. The consensus definition of TTR includes anastomotic or metastatic relapse, death with evidence of recurrence and death from CC cause. Conclusion: Standardised definitions of TTE end-points ensure the reproducibility of the end-points between RCTs and facilitate cross-trial comparisons. These definitions should be integrated in standard practice for the design, reporting and interpretation of adjuvant CC RCTs.
AB - Background: The variability of definitions for time-to-event (TTE) end-points impacts the conclusions of randomised clinical trials (RCTs). The Definition for the Assessment of Time-to-event Endpoints in CANcer (DATECAN) initiative aims to provide consensus definitions for TTE end-points used in RCTs. Here, we formulate guidelines for adjuvant colon cancer RCTs. Methods: We performed a literature review to identify TTE end-points and events included in their definition in RCT publications. Then, a consensus was reached among a panel of international experts, using a formal modified Delphi method, with 2 rounds of questionnaires and an in-person meeting. Results: Twenty-four experts scored 72 events involved in 6 TTE end-points. Consensus was reached for 24%, 57% and 100% events after the first round, second round and in-person meeting. For RCTs not using overall survival as their primary end-point, the experts recommend using disease-free survival (DFS) rather than recurrence-free survival (RFS) or time to recurrence (TTR) as the primary end-point. The consensus definition of DFS includes all causes of death, second primary colorectal cancers (CRCs), anastomotic relapse and metastatic relapse as an event, but not second primary non-CRCs. Events included in the RFS definition are the same as for DFS with the exception of second primary CRCs. The consensus definition of TTR includes anastomotic or metastatic relapse, death with evidence of recurrence and death from CC cause. Conclusion: Standardised definitions of TTE end-points ensure the reproducibility of the end-points between RCTs and facilitate cross-trial comparisons. These definitions should be integrated in standard practice for the design, reporting and interpretation of adjuvant CC RCTs.
KW - Adjuvant
KW - Chemotherapy
KW - Colon cancer
KW - Guidelines
KW - Randomised controlled trials
KW - Time-to-event end-points
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U2 - 10.1016/j.ejca.2020.02.009
DO - 10.1016/j.ejca.2020.02.009
M3 - Article
C2 - 32172199
AN - SCOPUS:85081223001
SN - 0959-8049
VL - 130
SP - 63
EP - 71
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -