Evidence map›Paper›PMID 28601342›Full record

Trial reportLancet (London, England)2017

Organ preservation for rectal cancer (GRECCAR 2): a prospective, randomised, open-label, multicentre, phase 3 trial.

Eric Rullier, Philippe Rouanet, Jean-Jacques Tuech, Alain Valverde, Bernard Lelong, Michel Rivoire, Jean-Luc Faucheron, Mehrdad Jafari, Guillaume Portier, Bernard Meunier and 10 more

3 registry-linked trialsAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Lancet (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 159 papers, 20 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
159citing papers in PubMed, 20 pooled it
18.7field-weighted citation impact, top 1% of its field
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.

NCT00427375 phase3completednot on this map

Phase III Randomized Trial of Local Excision Versus Total Mesorectal Excision in Downstaged T2T3 Low Rectal Cancer After Radiochemotherapy

TypeinterventionalSponsorUniversity Hospital, BordeauxRan2007 to 2018Enrolled148ConditionsRectal NeoplasmsArmslocal rectal excision, total mesorectal excision
NCT03569488 unknown statusnot on this mapstarted 2020, after this paper: background citation

Validation of the French Version of the Low Anterior Resection Syndrome (LARS) Score for Measuring Bowel Dysfunction After Sphincter-preserving Surgery Among Rectal Cancer Patients

TypeobservationalSponsorUniversity Hospital, CaenRan2020 to 2024Enrolled1,100ConditionsRectal Cancer PatientsArmsFT-LARS questionnaire
NCT04103567 narecruitingnot on this mapstarted 2020, after this paper: background citation

Determination of Microbiological Factors Associated With Poor Response to Neoadjuvant Therapy in Rectal Cancers: Focus on Cyclomodulin-producing Escherichia Coli

TypeinterventionalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2020 to 2030Enrolled220ConditionsRectal CancerArmsBiological collection
3 · Its place in the literature

Who cites it

159 citing papers in PubMed, 20 syntheses or guidelines pooled it, 374 citations in OpenAlex.

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  13. COVID-19 epidemic: Proposed alternatives in the management of digestive cancers: A French intergroup clinical point of view (SNFGE, FFCD, GERCOR, UNICANCER, SFCD, SFED, SFRO, SFR).Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2020
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99 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 16 institutions in 1 country.

Eric RullierDepartment of Colorectal Surgery, Haut-Lévèque Hospital, Pessac, CHU Bordeaux, France. Electronic address: eric.rullier@chu-bordeaux.fr.
Philippe RouanetDépartement de Chirurgie Oncologique, ICM Val d'Aurelle, Montpellier, France.
Jean-Jacques TuechService de Chirurgie Digestive, CHU Charles Nicolle, Rouen, France.
Alain ValverdeService de Chirurgie Digestive, Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.
Bernard LelongDépartement de Chirurgie Oncologique, Institut Paoli Calmette, Marseille, France.
Michel RivoireDépartement de Chirurgie Oncologique, Centre Léon Bérard, Lyon, France.
Jean-Luc FaucheronService de Chirurgie Digestive, Hôpital A Michallon, La Tronche, France.
Mehrdad JafariDépartement de Chirurgie Oncologique, Centre Oscar Lambret, Lille, France.
Guillaume PortierService de Chirurgie Digestive, Hôpital Purpan, Toulouse, France.
Bernard MeunierService de Chirurgie Viscérale, CHU Pontchaillou, Rennes, France.
Igor SileznieffService de Chirurgie Digestive, CHU Timone, Marseille, France.
Michel PrudhommeDépartement de Chirurgie Digestive et de Cancérologie Digestive, Hôpital Universitaire Carémeau, Nimes, France.
Frédéric MarchalDépartement de Chirurgie Oncologique, Institut de Cancérologie de Lorraine, CRAN, UMR 7039, Université de Lorraine, CNRS, Vandoeuvre les Nancy, France.
Marc PocardDépartement Médico-Chirurgical de Pathologie Digestive, Hôpital Lariboisière, Paris, France.
Denis PezetService de Chirurgie Générale et Digestive, Hôtel Dieu, Clermont-Ferrand, France.
Anne RullierService d'Anatomopathologie, Hôpital Pellegrin, Bordeaux, CHU Bordeaux, France.
Véronique VendrelyService de Radiothérapie, Haut-Lévèque Hospital, Pessac, CHU Bordeaux, France.
Quentin DenostDepartment of Colorectal Surgery, Haut-Lévèque Hospital, Pessac, CHU Bordeaux, France.
Julien AsselineauUnité de Soutien Méthodologique à la Recherche Clinique et Epidémiologique du CHU de Bordeaux, Université Bordeaux, Bordeaux, France.
Adélaïde DoussauUnité de Soutien Méthodologique à la Recherche Clinique et Epidémiologique du CHU de Bordeaux, Université Bordeaux, Bordeaux, France.
Hôpital Cardiologique du Haut-Lévêque · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Nîmes · FRCentre Léon Bérard · FRCentre National de la Recherche Scientifique · FRCentre Oscar Lambret · FRGroupe Hospitalier Diaconesses Croix Saint-Simon · FRHôpital Albert Michallon · FRHôpital Charles-Nicolle · FRHôpital de la Timone · FRHôpital Lariboisière · FRHôpital Pellegrin · FRHôpital Pontchaillou · FRHôpital Purpan · FRHôtel-Dieu de Lyon · FRInstitut Paoli-Calmettes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOrgan preservation is a concept proposed for patients with rectal cancer after a good clinical response to neoadjuvant chemotherapy, to potentially avoid morbidity and side-effects of rectal excision. The objective of this study was to compare local excision and total mesorectal excision in patients with a good response after chemoradiotherapy for lower rectal cancer.

methodsWe did a prospective, randomised, open-label, multicentre, phase 3 trial at 15 tertiary centres in France that were experts in the treatment of rectal cancer. Patients aged 18 years and older with stage T2T3 lower rectal carcinoma, of maximum size 4 cm, who had a good clinical response to neoadjuvant chemoradiotherapy (residual tumour ≤2 cm) were centrally randomly assigned by the surgeon before surgery to either local excision or total mesorectal excision surgery. Randomisation, which was done via the internet, was not stratified and used permuted blocks of size eight. In the local excision group, a completion total mesorectal excision was required if tumour stage was ypT2-3. The primary endpoint was a composite outcome of death, recurrence, morbidity, and side-effects at 2 years after surgery, to show superiority of local excision over total mesorectal excision in the modified intention-to-treat (ITT) population (expected proportions of patients having at least one event were 25% vs 60% for superiority). This trial was registered with ClinicalTrials.gov, number NCT00427375.

findingsFrom March 1, 2007, to Sept 24, 2012, 186 patients received chemoradiotherapy and were enrolled in the study. 148 good clinical responders were randomly assigned to treatment, three were excluded (because they had metastatic disease, tumour >8 cm from anal verge, and withdrew consent), and 145 were analysed: 74 in the local excision group and 71 in the total mesorectal excision group. In the local excision group, 26 patients had a completion total mesorectal excision. At 2 years in the modified ITT population, one or more events from the composite primary outcome occurred in 41 (56%) of 73 patients in the local excision group and 33 (48%) of 69 in the total mesorectal excision group (odds ratio 1·33, 95% CI 0·62-2·86; p=0·43). In the modified ITT analysis, there was no difference between the groups in all components of the composite outcome, and superiority was not shown for local excision over total mesorectal excision.

interpretationWe failed to show superiority of local excision over total mesorectal excision, because many patients in the local excision group received a completion total mesorectal excision that probably increased morbidity and side-effects, and compromised the potential advantages of local excision. Better patient selection to avoid unnecessary completion total mesorectal excision could improve the strategy.

fundingNational Cancer Institute of France, Sanofi, Roche Pharma.

Indexed as

AdultAgedAged, 80 and overChemoradiotherapy, AdjuvantFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNeoadjuvant TherapyNeoplasm StagingOrgan PreservationPostoperative ComplicationsProspective StudiesRectal NeoplasmsRecurrence

Identifiers

PMID28601342
OpenAlexW2623430466

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.