Web of Science: 5 citas, Scopus: 7 citas, Google Scholar: citas,
Proxies of quality of life in metastatic colorectal cancer : analyses in the RECOURSE trial
Van Cutsem, Eric (University Hospitals Leuven and KU Leuven)
Falcone, Alfredo (Azienda Ospedaliero-Universitaria Pisana)
García Carbonero, Rocio (Hospital Universitario 12 de Octubre/i+12)
Komatsu, Yoshito (Hokkaido University Hospital)
Pastorino, Alessandro (IRCCS AOU San Martino IST)
Peeters, Marc (Antwerp University Hospital)
Shimada, Yasuhiro (National Cancer Center Hospital)
Yamazaki, Kentaro (Shizuoka Cancer Center)
Yoshino, Takayuki (National Cancer Center Hospital East)
Zaniboni, Alberto (Fondazione Poliambulanza)
Amellal, Nadia (Institut de Recherches Servier)
Kanehisa, Akira (Institut de Recherches Servier)
Winkler, Robert (Taiho Oncology)
Makris, Lukas (Taiho Oncology)
Mayer, Robert J (Dana-Farber Cancer Institute)
Ohtsu, Atsushi (National Cancer Center Hospital East)
Tabernero Caturla, Josep (Universitat Autònoma de Barcelona. Deaprtament de Medicina)

Fecha: 2017
Resumen: In the pivotal phase III, randomised, double-blind, placebo-controlled RECOURSE study, treatment with trifluridine/tipiracil was well tolerated and associated with prolonged progression-free and overall survival in patients with metastatic colorectal cancer (mCRC). There was no formal analysis of quality of life (QoL) in RECOURSE. The aim of the present analysis was to assess proxies of QoL during the RECOURSE treatment period, in terms of adverse events (AEs) likely to affect QoL and Eastern Cooperative Oncology Group performance status (ECOG PS). Enrolled patients had documented, previously treated (≥2 prior chemotherapy lines) mCRC and an ECOG PS of 0 or 1. Patients received best supportive care plus trifluridine/tipiracil 35 mg/m 2 twice daily (n=534) or placebo (n=266) in a 28-day cycle. AEs analysed included nausea, vomiting, diarrhoea, dysgeusia and fatigue/asthenia. ECOG PS was determined at baseline, on day 1 of each treatment cycle, at treatment end and 30 days post-treatment discontinuation. AEs that affect QoL were more frequent in patients treated with trifluridine/tipiracil than placebo. Median treatment duration for patients experiencing at least one of these AEs was longer than that observed for the overall RECOURSE population (trifluridine/tipiracil: 12 vs 7 weeks; placebo: 10 vs 6 weeks). Versus placebo, the duration of most AEs was longer in trifluridine/tipiracil recipients; however, all AEs except nausea and vomiting occupied a lower proportion of the total treatment period. Of the patients who had their PS recorded at discontinuation, PS was maintained in 67% and 63% of trifluridine/tipiracil and placebo recipients, and 84% and 81% of the trifluridine/tipiracil and placebo patients remained at a PS of 0 or 1 at discontinuation. Analysis of ECOG PS and AEs thought to affect QoL in the RECOURSE patient population suggests that trifluridine/tipiracil treatment does not result in a deterioration of patient QoL versus placebo.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. Creative Commons
Lengua: Anglès.
Documento: article ; recerca ; publishedVersion
Materia: Advanced colorectal cancer ; Trifluridine/tipiracil ; Quality of life ; Performance status
Publicado en: ESMO Open, Vol. 2 (november 2017) , ISSN 2059-7029

PMID: 29215098
DOI: 10.1136/esmoopen-2017-000261

7 p, 770.6 KB

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 Registro creado el 2018-02-08, última modificación el 2019-05-09

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