Evidence map›Paper›PMID 40324123›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Characteristics of Patients and Prognostic Factors Across Treatment Lines in Metastatic Colorectal Cancer: An Analysis From the Aide et Recherche en Cancérologie Digestive Database.

Jean-Baptiste Bachet, Aimery de Gramont, Morteza Raeisi, Manel Rakez, Richard M Goldberg, Niall C Tebbutt, Eric Van Cutsem, Daniel G Haller, J Randolph Hecht, Robert J Mayer and 11 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Upfront Modified FOLFOXIRI Plus Panitumumab forJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Trial
  2. Article
  3. First-line treatment efficacy and prognostic model in RAS-mutant metastatic colorectal cancer: a real-world study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  4. Article
  5. Article
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

21 authors.

Jean-Baptiste BachetHepato-gastroenterology and Digestive Oncology Department, Pitié Salpêtrière Hospital, APHP, Sorbonne Université, Paris, France.ORCID 0000-0003-4337-286X
Aimery de GramontDepartment of Medical Oncology, Franco-British Hospital, Fondation Cognacq-Jay, Cancérologie Paris Ouest, Levallois-Perret, France.ORCID 0000-0001-7940-9877
Morteza RaeisiStatistical Unit, ARCAD Foundation, Paris, France.ORCID 0000-0002-9999-4097
Manel RakezStatistical Unit, ARCAD Foundation, Paris, France.ORCID 0000-0003-1516-7893
Richard M GoldbergDepartment of Medicine, West Virginia University Cancer Institute, Morgantown, WV.ORCID 0000-0003-0308-8223
Niall C TebbuttDepartment of Medical Oncology, Olivia Newton-John Cancer, Wellness and Research Centre, Austin Health, Heidelberg, VIC, Australia.ORCID 0000-0003-2613-5168
Eric Van CutsemDigestive Oncology, University Hospitals Leuven and KU Leuven, Leuven, Belgium.ORCID 0000-0002-6372-1230
Daniel G HallerAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
J Randolph HechtUCLA Jonsson Comprehensive Cancer Center, Santa Monica, CA.ORCID 0000-0003-2277-4157
Robert J MayerDana-Farber Cancer Institute, Boston, MA.
Stuart M LichtmanWilmot Cancer Institute Geriatric Oncology Research Group, University of Rochester, Rochester, NY.ORCID 0000-0003-4146-6192
Al B BensonDivision of Hematology/Oncology, Northwestern University's Feinberg School of Medicine, Chicago, IL.ORCID 0000-0001-5485-7227
Alberto F SobreroDepartment of Medical Oncology, Ospedale San Martino, Genoa, Italy.ORCID 0000-0001-5483-4412
Josep TaberneroVall d'Hebron Hospital Campus and Vall d'Hebron Institute of Oncology (VHIO), IOB-Quiron, Barcelona, Spain.ORCID 0000-0002-2495-8139
Richard AdamsCardiff University and Velindre Cancer Centre, Cardiff, United Kingdom.ORCID 0000-0003-3915-7243
John R ZalcbergDepartment of Medical Oncology, Monash University School of Public Health and Preventive Medicine, Alfred Health, Melbourne, VIC, Australia.
Axel GrotheyWest Cancer Center, Germantown, TN.
Takayuki YoshinoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0002-0489-4756
Thierry AndréARCAD Foundation, Paris, France.ORCID 0000-0002-5103-7095
Qian ShiDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.ORCID 0000-0002-4640-8832
Benoist ChibaudelDepartment of Medical Oncology, Franco-British Hospital, Fondation Cognacq-Jay, Cancérologie Paris Ouest, Levallois-Perret, France.ORCID 0000-0003-1279-2044

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSeveral lines of treatment can be used sequentially in patients with metastatic colorectal cancer. We investigated the evolution of patient/tumor characteristics and their prognostic impact across treatment lines to develop an overall prognostic score (OPS). PATIENTS AND

methodsIndividual patient data from 48 randomized trials were analyzed. The end point was overall survival (from random assignment to death). Missing data were imputed. The complete data set was then separated into construction (80%) and validation sets (20%). The Cox's model was used to define risk groups for survival using the OPS. The discrimination capability was assessed in each treatment-line via bootstrapping to obtain optimism-corrected calibration and discrimination C-indices. Internal validation was done in the validation set.

resultsA total of 37,560 patients (26,974 in first-line [1L], 7,693 in second-line [2L], and 2,893 in third-line [3L]) were analyzed. Some clinical, biological, and molecular characteristics of patients/tumors included in therapeutic trials evolve over the lines. Seven independent prognostic variables were retained in the final multivariate model common to all lines: Eastern Cooperative Oncology Group performance status, hemoglobin, platelet count, WBC/absolute neutrophil count ratio, lactate dehydrogenase, alkaline phosphatase, and the number of metastatic sites. The OPS was used to define four patient subgroups with significantly different prognoses in 1L, 2L, and 3L, separately, with adequate C-indices: 0.65, 0.66, and 0.69 in the construction set and 0.65, 0.66, and 0.68 in the validation set, respectively. The OPS was not predictive, with 3L drugs (

conclusionThe same prognostic model using practical variables can be used before all treatment lines. The OPS could better stratify patients in future clinical trials and help to therapeutic decision in routine practice.

Indexed as

Colorectal NeoplasmsAgedDatabases, FactualFemaleHumansMaleMiddle AgedNeoplasm MetastasisPrognosisProportional Hazards ModelsRandomized Controlled Trials as Topic

Identifiers

PMID40324123
PMCPMC12169864

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Registered trials

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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.