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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMacarulla Mercadé, Teresa
dc.contributor.authorChen, Li-Tzong
dc.contributor.authorSiveke, Jens T.
dc.contributor.authorBodoky, György
dc.contributor.authorLi, Chung-Pin
dc.contributor.authorCunningham, David
dc.date.accessioned2021-11-17T12:43:16Z
dc.date.available2021-11-17T12:43:16Z
dc.date.copyright2019
dc.date.issued2020-01
dc.identifier.citationMacarulla Mercadé T, Chen LT, Li CP, Siveke JT, Cunningham D, Bodoky G, et al. Liposomal Irinotecan + 5-FU/LV in Metastatic Pancreatic Cancer: Subgroup Analyses of Patient, Tumor, and Previous Treatment Characteristics in the Pivotal NAPOLI-1 Trial. Pancreas. 2020 Jan;49(1):62–75.
dc.identifier.issn1536-4828
dc.identifier.urihttps://hdl.handle.net/11351/6557
dc.descriptionMetastatic Pancreatic Cancer; Previous Treatment; Irinotecan
dc.description.abstractObjectives The NAnoliPOsomaL Irinotecan (NAPOLI-1) study (NCT01494506) was the largest global phase 3 study in a post-gemcitabine metastatic pancreatic adenocarcinoma (mPAC) population (N = 417). The subanalyses reported here investigated the prognostic effect of tumor characteristics and disease stage, prior treatment characteristics, baseline patient characteristics on survival outcomes in NAPOLI-1, and whether liposomal irinotecan (nal-IRI) + 5-fluorouracil/leucovorin (5-FU/LV) benefited patients with mPAC across subgroups. Methods Post hoc analyses were performed in the NAPOLI-1 population (4 across tumor characteristics and disease stage, 6 across prior treatment characteristics, and 4 across patient baseline characteristics). Survival outcomes were estimated by Kaplan-Meier analysis and patient safety data were evaluated. Results Mortality and morbidity risk was lower on nal-IRI+5-FU/LV treatment across subgroups. Exceptions were patients who had received prior nonliposomal irinotecan and those who had undergone prior Whipple procedure (overall survival hazard ratio = 1.25 and 1.23, respectively). Decreased appetite, liver metastases, and number of measurable metastatic lesions seemed to be prognostic of survival in this population. Subgroup safety data were generally comparable with those in the overall NAPOLI-1 safety population. Conclusions A diverse population of patients with mPAC that progressed on gemcitabine-based therapy benefited from nal-IRI+5-FU/LV versus 5-FU/LV, potentially helping guide treatment decisions for challenging cases.
dc.language.isoeng
dc.publisherWolters Kluwer Health
dc.relation.ispartofseriesPancreas;49(1)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPàncrees - Càncer - Tractament
dc.subjectPàncrees - Càncer - Prognosi
dc.subject.meshPancreatic Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshTreatment Outcome
dc.titleLiposomal Irinotecan + 5-FU/LV in Metastatic Pancreatic Cancer: Subgroup Analyses of Patient, Tumor, and Previous Treatment Characteristics in the Pivotal NAPOLI-1 Trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1097/MPA.0000000000001455
dc.subject.decsneoplasias pancreáticas
dc.subject.decs/farmacoterapia
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.1097/MPA.0000000000001455
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Macarulla Mercadé T] Vall d'Hebron Hospital Universitari, Barcelona, Spain. Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Chen LT] National Institute of Cancer Research, National Health Research Institutes. Department of Internal Medicine, National Cheng Kung University Hospital, National Cheng Kung University, Tainan. [Li CP] Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital. National Yang-Ming University School of Medicine, Taipei, Taiwan. [Siveke JT] Division of Solid Tumor Translational Oncology, West German Cancer Center, University Hospital Essen. German Cancer Consortium (DKTK, partner site Essen) and German Cancer Research Center, DKFZ, Heidelberg, Germany. [Cunningham D] The Royal Marsden NHS Foundation Trust, London and Surrey, United Kingdom. [Bodoky G] Department of Oncology, Szent László Hospital, Budapest, Hungary
dc.identifier.pmid31856081
dc.identifier.wos000503790800006
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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