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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorSobrero, Alberto
dc.contributor.authorDasari, Arvind
dc.contributor.authorJeneth Aquino, Jeneth Aquino
dc.contributor.authorElez, Elena
dc.contributor.authorLonardi, Sara
dc.contributor.authorGarcia-Carbonero, Rocio
dc.contributor.authorTabernero, Josep
dc.date.accessioned2025-04-02T12:40:35Z
dc.date.available2025-04-02T12:40:35Z
dc.date.issued2025-03-11
dc.identifier.citationSobrero A, Dasari A, Aquino J, Lonardi S, Garcia-Carbonero R, Elez E, et al. Health-related quality of life associated with fruquintinib in patients with metastatic colorectal cancer: Results from the FRESCO-2 study. Eur J Cancer. 2025 Mar 11;218:115268.
dc.identifier.issn0959-8049
dc.identifier.urihttp://hdl.handle.net/11351/12884
dc.descriptionFruquintinib; Health-related quality of life; Metastatic colorectal cancer
dc.description.abstractIntroduction Maintaining or improving health-related quality of life (HRQoL) is as important as extending survival in metastatic colorectal cancer. We report an HRQoL analysis from FRESCO-2 (NCT04322539). Methods Patients were randomized to fruquintinib +best supportive care (BSC; n = 461) or placebo +BSC (n = 230). Instruments of EORTC QLQ-C30 and 5-level EQ-5D, and ECOG performance status (PS) were assessed. Changes from baseline scores for QLQ-C30 and EQ-5D were evaluated and minimally important difference thresholds were used to define stable, improved, or deteriorated QoL. Time to deterioration (TTD) was assessed. Results With fruquintinib versus placebo, baseline QLQ-C30 global health status (GHS) and EQ-5D visual analog scale (VAS) scores were 65.2 versus 64.6 and 67.0 versus 66.6, respectively. Least-squares mean changes from baseline fluctuated throughout treatment. At end of treatment (EOT), mean scores with fruquintinib versus placebo were 53.8 versus 52.3 (QLQ-C30 GHS) and 58.9 versus 58.5 (EQ-5D VAS). For QLQ-C30 GHS, 38.3 % versus 36.5 % of patients receiving fruquintinib versus placebo had stable or improved scores at EOT; median TTD was 2.1 versus 1.8 months (HR, 0.9; 95 % CI, 0.7–1.0). For EQ-5D VAS, 47.9 % versus 42.7 % had stable or improved scores at EOT; median TTD was 2.6 versus 1.9 months (HR, 0.8; 95 % CI, 0.6–0.9). Median TTD to ECOG PS ≥ 2 or death within 30+ /7 days after EOT was 6.6 versus 2.9 months with fruquintinib versus placebo (HR, 0.6; 95 % CI, 0.4–0.7). Conclusions Fruquintinib delayed TTD of ECOG PS and did not negatively impact HRQoL versus placebo.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesEuropean Journal of Cancer;218
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectCòlon - Càncer - Tractament
dc.subjectRecte - Càncer - Tractament
dc.subjectMetàstasi
dc.subjectPacients - Satisfacció
dc.subjectProteïnes quinases - Inhibidors - Ús terapèutic
dc.subject.meshProtein-Tyrosine Kinases
dc.subject.mesh/antagonists & inhibitors
dc.subject.meshQuality of Life
dc.subject.meshNeoplasm Metastasis
dc.subject.meshColorectal Neoplasms
dc.subject.mesh/drug therapy
dc.titleHealth-related quality of life associated with fruquintinib in patients with metastatic colorectal cancer: Results from the FRESCO-2 study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ejca.2025.115268
dc.subject.decsproteína-tirosina cinasas
dc.subject.decs/antagonistas & inhibidores
dc.subject.decscalidad de vida
dc.subject.decsmetástasis neoplásica
dc.subject.decsneoplasias colorrectales
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.1016/j.ejca.2025.115268
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Sobrero A] Department of Medical Oncology, Azienda Ospedaliera San Martino, Genoa, Italy. [Dasari A] Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. [Aquino J] Vanderbilt University School of Medicine, Nashville, TN, USA. [Lonardi S] Medical Oncology Unit 1, Veneto Institute of Oncology IOV-IRCCS Padua, Padua, Italy. [Garcia-Carbonero R] Oncology Department, Hospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria lmas12, Facultad de Medicina UCM, CIBERONC, Madrid, Spain. [Elez E, Tabernero J] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. CIBERONC, Barcelona, Spain
dc.identifier.pmid39952149
dc.identifier.wos001427842800001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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