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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorBACHET, Jean-Baptiste
dc.contributor.authorde Gramont, Aimery
dc.contributor.authorRaeisi, Morteza
dc.contributor.authorRAKEZ, Manel
dc.contributor.authorGoldberg, Richard
dc.contributor.authorTebbutt, Niall
dc.contributor.authorTabernero, Josep
dc.date.accessioned2025-07-08T07:05:47Z
dc.date.available2025-07-08T07:05:47Z
dc.date.issued2025-06-20
dc.identifier.citationBachet JB, de Gramont A, Raeisi M, Rakez M, Goldberg RM, Tebbutt NC, et al. Characteristics of Patients and Prognostic Factors Across Treatment Lines in Metastatic Colorectal Cancer: An Analysis From the Aide et Recherche en Cancérologie Digestive Database. J Clin Oncol. 2025 Jun 20;43(18):2094-106.
dc.identifier.issn1527-7755
dc.identifier.urihttp://hdl.handle.net/11351/13364
dc.descriptionPrognostic factors; Metastatic colorectal cancer
dc.description.abstractPurpose: Several 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 methods: Individual 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. Results: A 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 (v placebo) or subsequent line (2L/1L or 3L/2L) extending survival in all prognostic groups. Conclusion: The 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.
dc.language.isoeng
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofseriesJournal of Clinical Oncology;43(18)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectCòlon - Càncer - Tractament
dc.subjectRecte - Càncer - Tractament
dc.subjectCòlon - Càncer - Prognosi
dc.subjectRecte - Càncer - Prognosi
dc.subject.meshColorectal Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshPrognosis
dc.titleCharacteristics of Patients and Prognostic Factors Across Treatment Lines in Metastatic Colorectal Cancer: An Analysis From the Aide et Recherche en Cancérologie Digestive Database
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO-24-01968
dc.subject.decsneoplasias colorrectales
dc.subject.decs/farmacoterapia
dc.subject.decspronóstico
dc.relation.publishversionhttps://doi.org/10.1200/JCO-24-01968
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Bachet JB] Hepato-gastroenterology and Digestive Oncology Department, Pitié Salpêtrière Hospital, APHP, Sorbonne Université, Paris, France. [de Gramont A] Department of Medical Oncology, Franco-British Hospital, Fondation Cognacq-Jay, Cancérologie Paris Ouest, Levallois-Perret, France. ARCAD Foundation, Paris, France. [Raeisi M, Rakez M] Statistical Unit, ARCAD Foundation, Paris, France. [Goldberg RM] Department of Medicine, West Virginia University Cancer Institute, Morgantown, WV. [Tebbutt NC] Department of Medical Oncology, Olivia Newton-John Cancer, Wellness and Research Centre, Austin Health, Heidelberg, VIC, Australia. [Tabernero J] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. IOB-Quiron, Barcelona, Spain
dc.identifier.pmid40324123
dc.identifier.wos001507605800001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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