| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Chandana, Sreenivasa R |
| dc.contributor.author | Kiss, Igor |
| dc.contributor.author | Melisi, Davide |
| dc.contributor.author | Macarulla, Teresa |
| dc.contributor.author | DE LA FOUCHARDIERE, CHRISTELLE |
| dc.contributor.author | Pazo-Cid, Roberto A. |
| dc.date.accessioned | 2025-10-03T10:36:49Z |
| dc.date.available | 2025-10-03T10:36:49Z |
| dc.date.issued | 2025-08 |
| dc.identifier.citation | Melisi 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.issn | 2059-7029 |
| dc.identifier.uri | http://hdl.handle.net/11351/13771 |
| dc.description | Gemcitabine; Health-related quality of life; Nab-paclitaxel |
| dc.description.abstract | Background
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.iso | eng |
| dc.publisher | Elsevier |
| dc.relation.ispartofseries | ESMO Open;10(8) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Qualitat de vida |
| dc.subject | Pàncrees - Càncer - Tractament |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic |
| dc.subject | Metàstasi |
| dc.subject.mesh | Pancreatic Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Quality of Life |
| dc.subject.mesh | Carcinoma, Pancreatic Ductal |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Morbid Metastasis |
| dc.title | 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 |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1016/j.esmoop.2025.105534 |
| dc.subject.decs | neoplasias pancreáticas |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | calidad de vida |
| dc.subject.decs | carcinoma ductal pancreático |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | metástasis neoplásica |
| dc.relation.publishversion | https://doi.org/10.1016/j.esmoop.2025.105534 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 40763412 |
| dc.identifier.wos | 001545821900002 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |