Evidence map›Paper›PMID 32172199›Full record

ArticleEuropean journal of cancer (Oxford, England : 1990)2020

Guidelines for time-to-event end-point definitions in adjuvant randomised trials for patients with localised colon cancer: Results of the DATECAN initiative.

Romain Cohen, Dewi Vernerey, Carine Bellera, Aurélia Meurisse, Julie Henriques, Xavier Paoletti, Benoît Rousseau, Steven Alberts, Thomas Aparicio, Ioannis Boukovinas and 29 more

2 registry-linked trialsAbstract read
In one paragraph

Article in European journal of cancer (Oxford, England : 1990), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03676010 active not recruitingnot on this map

Definition for the Assessment of Time-to-event Endpoints in CANcer Trials (DATECAN-1) : Formal Consensus Method for the Development of Guidelines for Standardized Time-to-event Endpoints' Definitions in Cancer Clinical Trials

TypeobservationalSponsorInstitut BergoniéRan2009 to 2026Enrolled265ConditionsCancerArmsSarcoma and GIST, Breast cancer, Pancreatic cancer, Renal cell carcinoma, Colon cancer
NCT07369531 narecruitingnot on this mapstarted 2026, after this paper: background citation

The Impact of Two-Stage Turnbull-Cutait Pull-Through Coloanal Anastomosis on Stoma-free Survival in Low Rectal Anal-preserving Surgery: A Multicenter Randomized Controlled Trial (FIAS)

TypeinterventionalSponsorThe First Hospital of Jilin UniversityRan2026 to 2031Enrolled520ConditionsRectal Cancer, Surgical Anastomosis, Survival , Tumor, Anal FunctionArmsTurnbull-Cutait anastomosis, LAR
3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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  12. Oxaliplatin-Based Adjuvant Chemotherapy in Older Patients With Stage III Colon Cancer: An ACCENT/IDEA Pooled Analysis of 12 Trials.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

39 authors.

Romain CohenSorbonne Université, Department of Medical Oncology, AP-HP, Hôpital Saint-Antoine, F-7512, Paris, France; Division of Biomedical Statistics and Informatics, Department of Health Science Research, Mayo Clinic, Rochester, MN, USA. Electronic address: romain.cohen@aphp.fr.
Dewi VernereyMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, F-25000, Besançon, France; University Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Carine BelleraUniv. Bordeaux, Inserm, Bordeaux Population Health Research Center, Epicene Team, UMR 1219, F-33000 Bordeaux, France; Inserm CIC1401, Clinical and Epidemiological Research Unit, Institut Bergonié, Comprehensive Cancer Center, F-33000, Bordeaux, France.
Aurélia MeurisseMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, F-25000, Besançon, France; University Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Julie HenriquesMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, F-25000, Besançon, France; University Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Xavier PaolettiUniversité de Versailles-St Quentin & Institut Curie, INSERM U900, équipe Biostatistique, France.
Benoît RousseauMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Steven AlbertsDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Thomas AparicioService de Gastroentérologie et Cancérologie Digestive, Hôpital Saint Louis, APHP, Université de Paris, Paris, France.
Ioannis BoukovinasBioclinic Oncology Unit of Thessaloniki, Thessaloniki, France.
Sharlene GillBC Cancer, Vancouver, Canada.
Richard M GoldbergWest Virginia University Cancer Institute, Morgantown WV, USA.
Axel GrotheyWest Cancer Center and Research Institute, Germantown, TN, USA.
Tetsuya HamaguchiDepartment of Gastroenterological Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
Timothy IvesonUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Rachel KerrAdjuvant Colorectal Cancer Group, University of Oxford, UK.
Roberto LabiancaOspedale Papa Giovanni XXIII, Bergamo, Italy.
Sara LonardiIstituto Oncologico Veneto-IRCCS, Padova, Italy.
Jeffrey MeyerhardtDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.
James PaulCancer Research UK Clinical Trials Unit (CTU), Institute of Cancer Sciences, University of Glasgow, UK.
Cornelis J A PuntDepartment of Medical Oncology, Amsterdam University Medical Centers, University of Amsterdam, Netherlands.
Leonard SaltzMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Marck P SaundersDepartment of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Hans-Joachim SchmollEORTC GI Study Group, AIO Colorectal Cancer Group, Martin Luther University, Halle, Germany.
Manish ShahDepartment of Medicine, Division of Hematology and Medical Oncology, Center for Advanced Digestive Care, Weill Cornell Medicine, New York-Presbyterian Hospital, New York, NY, USA.
Alberto SobreroMedical Oncology Unit at Ospedale San Martino, Genova, Italy.
Ioannis SouglakosMedical School, University of Crete, Heraklion, Greece.
Julien TaiebSorbonne Paris Cité, Paris Descartes University, Department of Digestive Oncology, Georges Pompidou European Hospital, Paris, France.
Atsuo TakashimaNational Cancer Center Hospital, Tokyo, Japan.
Anna Dorothea WagnerDepartment of Oncology, Lausanne University Hospital and University of Lausanne, Switzerland.
Marc YchouDepartment of Medical Oncology, Institut Régional Du Cancer de Montpellier (ICM), France.
Franck BonnetainMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, F-25000, Besançon, France; University Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Sophie GourgouBiometrics Unit, Montpellier Cancer Institute, Univ Montpellier, Montpellier, France.
Takayuki YoshinoNational Cancer Center Hospital East, Kashiwa, Japan.
Greg YothersNRG Oncology and University of Pittsburgh, USA.
Aimery de GramontDepartment of Medical Oncology, Institut Hospitalier Franco Britannique, Levallois-Perret, France.
Qian ShiDivision of Biomedical Statistics and Informatics, Department of Health Science Research, Mayo Clinic, Rochester, MN, USA.
Thierry AndréSorbonne Université, Department of Medical Oncology, AP-HP, Hôpital Saint-Antoine, F-7512, Paris, France.
ACCENT Group

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
Network Lead Academic Participating Site: Memorial Sloan Kettering Cancer CenterUG1CA233290 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CAROL AGHAJANIAN, Darren Feldman · 2019 to 2026
$10.2M
NCTN Lead Academic Participating Site at Dana-Farber/Partners Cancer CareUG1CA233180 · NCI · DANA-FARBER CANCER INST · PI Harold John Burstein · 2019 to 2026
$8.6M
NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233290NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

backgroundThe 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.

methodsWe 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.

resultsTwenty-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.

conclusionStandardised 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.

Indexed as

Colonic NeoplasmsEndpoint DeterminationGuidelines as TopicHumansRandomized Controlled Trials as TopicReproducibility of ResultsResearch DesignAdjuvantChemotherapyColon cancerGuidelinesRandomised controlled trialsTime-to-event end-points

Identifiers

PMID32172199
PMCPMC7409551

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.