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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorAmellal, Nadia Causse
dc.contributor.authorCalleja, Edward
dc.contributor.authorFakih, Marwan
dc.contributor.authorPrager, M.D., Gerald
dc.contributor.authorTabernero, Josep
dc.contributor.authortaieb, julien
dc.date.accessioned2024-11-26T13:44:16Z
dc.date.available2024-11-26T13:44:16Z
dc.date.issued2024-11
dc.identifier.citationFakih M, Prager GW, Tabernero J, Amellal N, Calleja E, Taieb J. Clinically meaningful outcomes in refractory metastatic colorectal cancer: a decade of defining and raising the bar. ESMO Open. 2024 Nov;9(11):103931.
dc.identifier.issn2059-7029
dc.identifier.urihttps://hdl.handle.net/11351/12280
dc.descriptionColorectal cancer; Metastatic; Quality of life
dc.description.abstractCurrently, there is no consensus definition for clinically meaningful outcomes in randomized clinical trials (RCTs) designed to evaluate new treatments for patients with refractory metastatic colorectal cancer (mCRC). Since 2014, recommended targets for improvements in overall survival and progression-free survival have been published by several societies, including those from the American Society of Clinical Oncology (ASCO) Clinically Meaningful Outcomes Working Group in 2014, the European Society for Medical Oncology-Magnitude of Clinical Benefit Scale (ESMO-MCBS) in 2015, and Colorectal Cancer Canada (CCC) consensus statements in 2019. However, evidence from several systematic reviews suggests that in a substantial proportion of RCTs that led to oncology drug approvals, the recommended thresholds of ASCO and ESMO-MCBS were not met. In addition to efficacy and safety, quality of life (QoL) is important to patients with mCRC, especially for those who are receiving later-line therapy or end-of-life care. As such, both ESMO-MCBS and CCC recommend the inclusion of QoL assessments in the design of mCRC clinical trials. Since the publication of the ASCO recommendations in 2014, there has been significant progress in the development of treatment options for patients with refractory mCRC; these include the approvals of trifluridine/tipiracil (FTD/TPI) as a single agent and in combination with bevacizumab, and the approval of fruquintinib. Among the phase III RCTs in third-line mCRC, only the SUNLIGHT trial of FTD/TPI plus bevacizumab met all recommended thresholds for clinically meaningful improvements, while also demonstrating a manageable safety profile and slower deterioration in multiple measures of QoL compared with FTD/TPI alone. The results from the SUNLIGHT study show that incremental gains in several clinically meaningful endpoints are achievable, thus raising the bar in defining clinically meaningful outcomes for emerging therapies in refractory mCRC.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesESMO Open;9(11)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectRecte - Càncer - Tractament
dc.subjectCòlon - Càncer - Tractament
dc.subjectMetàstasi
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshColorectal Neoplasms
dc.subject.mesh/therapy
dc.subject.meshNeoplasm Metastasis
dc.subject.meshTreatment Outcome
dc.titleClinically meaningful outcomes in refractory metastatic colorectal cancer: a decade of defining and raising the bar
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.esmoop.2024.103931
dc.subject.decsneoplasias colorrectales
dc.subject.decs/terapia
dc.subject.decsmetástasis neoplásica
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.1016/j.esmoop.2024.103931
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Fakih M] Department of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, USA. [Prager GW] Department of Medicine I, Medical University Vienna, Vienna, Austria. [Tabernero J] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. IOB-Quiron, Barcelona, Spain. [Amellal N] Servier International Research Institute, Suresnes, France. [Calleja E] Taiho Oncology, Inc., Princeton, USA. [Taieb J] Gastroenterology and Gastrointestinal Oncology Department, Hôpital Européen Georges-Pompidou, University Paris-Cité (Paris Descartes), SIRC CARPEM, Paris, France
dc.identifier.pmid39395264
dc.identifier.wos001335373500001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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