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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorChandana, Sreenivasa R
dc.contributor.authorKiss, Igor
dc.contributor.authorMelisi, Davide
dc.contributor.authorMacarulla, Teresa
dc.contributor.authorDE LA FOUCHARDIERE, CHRISTELLE
dc.contributor.authorPazo-Cid, Roberto A.
dc.date.accessioned2025-10-03T10:36:49Z
dc.date.available2025-10-03T10:36:49Z
dc.date.issued2025-08
dc.identifier.citationMelisi D, Macarulla T, De La Fouchardière C, Pazo Cid RA, Chandana SR, Kiss I, et al. Health-related quality of life and performance status with NALIRIFOX versus nab-paclitaxel + gemcitabine in treatment-naive patients with metastatic pancreatic ductal adenocarcinoma: results from the NAPOLI 3 trial. ESMO Open. 2025 Aug;10(8):105534.
dc.identifier.issn2059-7029
dc.identifier.urihttp://hdl.handle.net/11351/13771
dc.descriptionGemcitabine; Health-related quality of life; Nab-paclitaxel
dc.description.abstractBackground In NAPOLI 3 (NCT04083235), first-line (1L) liposomal irinotecan plus 5-fluorouracil/leucovorin plus oxaliplatin (NALIRIFOX) demonstrated statistically significant improvements in overall survival and progression-free survival compared with gemcitabine plus nab-paclitaxel (Gem + NabP) in patients with metastatic pancreatic ductal adenocarcinoma (mPDAC). In this exploratory analysis, health-related quality of life (HRQoL) and performance status (PS) outcomes from NAPOLI 3 were evaluated. Materials and methods HRQoL was assessed at baseline, day 1 of each treatment cycle, and at end of treatment (EoT) using the European Organisation for Research and Treatment of Cancer Quality of Life core questionnaire (EORTC QLQ-C30). Analyses included patients who provided baseline and at least one subsequent assessment. A mixed model for repeated measures was used to describe score evolution over time between treatment arms. Eastern Cooperative Oncology Group (ECOG) PS was recorded in the intention-to-treat (ITT) population at baseline, days 1, 8, and 15 of each treatment cycle, and EoT. Time to deterioration (TTD) in EORTC QLQ-C30 and ECOG PS scores was estimated using the Kaplan–Meier methodology. Results Overall, 245 patients in the NALIRIFOX arm (ITT population, n = 383) and 232 patients in the Gem + NabP arm (n = 387) provided baseline and at least one subsequent EORTC QLQ-C30 assessment. There was an initial decline in global health status (GHS) from baseline to week 12 across both treatment arms [least-squares mean −2.4, 95% confidence interval (CI) −5.9 to 1.1; Gem + NabP: −0.7 (−4.2 to 2.9)], with no further deterioration from week 16 onwards. TTD in GHS (hazard ratio 0.74, 95% CI 0.53-1.04, nominal P = 0.08) and ECOG PS score (hazard ratio 0.72, 95% CI 0.55-0.92, nominal P = 0.009) was longer with NALIRIFOX than with Gem + NabP. Conclusions These data suggest that 1L NALIRIFOX provides efficacy benefits for patients with mPDAC without compromising HRQoL or PS compared with Gem + NabP.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesESMO Open;10(8)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectQualitat de vida
dc.subjectPàncrees - Càncer - Tractament
dc.subjectQuimioteràpia combinada
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subjectMetàstasi
dc.subject.meshPancreatic Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshQuality of Life
dc.subject.meshCarcinoma, Pancreatic Ductal
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshMorbid Metastasis
dc.titleHealth-related quality of life and performance status with NALIRIFOX versus nab-paclitaxel + gemcitabine in treatment-naive patients with metastatic pancreatic ductal adenocarcinoma: results from the NAPOLI 3 trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.esmoop.2025.105534
dc.subject.decsneoplasias pancreáticas
dc.subject.decs/farmacoterapia
dc.subject.decscalidad de vida
dc.subject.decscarcinoma ductal pancreático
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsmetástasis neoplásica
dc.relation.publishversionhttps://doi.org/10.1016/j.esmoop.2025.105534
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Melisi D] Investigational Cancer Therapeutics Clinical Unit, Azienda Ospedaliera Universitaria Integrata, Verona, Italy. Digestive Molecular Clinical Oncology Research Unit, Università degli studi di Verona, Verona, Italy. [Macarulla T] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [De La Fouchardière C] Centre Léon Bérard, Lyon, France. [Pazo Cid RA] Hospital Universitario Miguel Servet, Zaragoza, Spain. [Chandana SR] Cancer and Hematology Centers of Western Michigan, Grand Rapids, USA. [Kiss I] Masaryk Memorial Cancer Institute and Faculty of Medicine, Masaryk University, Brno, Czechia
dc.identifier.pmid40763412
dc.identifier.wos001545821900002
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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