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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorStockem, Chantal F.
dc.contributor.authorEinerhand, Sarah M. H.
dc.contributor.authorMiras, Isabel
dc.contributor.authorSalhi, Youssra
dc.contributor.authorPérez Calabuig, Esther
dc.contributor.authorBakaloudi, Dimitra Rafailia
dc.contributor.authorMorales-Barrera, Rafael
dc.contributor.authorCarles, Joan
dc.date.accessioned2025-01-08T09:43:03Z
dc.date.available2025-01-08T09:43:03Z
dc.date.issued2024-10-23
dc.identifier.citationStockem CF, Einerhand SMH, Miras Rodríguez I, Salhi Y, Pérez E, Bakaloudi DR, et al. Long-term survival following anti-PD-(L)1 monotherapy in advanced urothelial cancer and an assessment of potential prognostic clinical factors: a multicentre observational study. BJC Reports. 2024 Oct 23;2:84.
dc.identifier.issn2731-9377
dc.identifier.urihttps://hdl.handle.net/11351/12378
dc.descriptionLong-term survival; Monotherapy; Advanced urothelial cancer
dc.description.abstractBackground Anti-PD-(L)1 agent are approved as first- and second-line treatment options in advanced urothelial cancer (UC), but information about long-term survival is scarce. There is a need for prognostic factors, as these may help in the decision-making concerning anti-PD-(L)1 in patients with UC. Here, we examined long-term survival following anti-PD-(L)1 in advanced UC and assessed clinical factors for their correlation with survival. Methods We collected data from patients with advanced UC treated with anti-PD-(L)1 between 2013 and 2023. Overall- and progression-free survival (OS, PFS) were determined using the Kaplan-Meier method. Independent variables were analysed by uni- and multivariate Cox regression for their association with OS and PFS. Results Survival analyses included 552 patients. Patient characteristics in our cohort were consistent with those of a typical advanced UC population. After median follow-up of 49 months, five-year OS and PFS rates were 16.0% and 6.9% respectively. The absence of visceral and/or bone metastases and elevated C-reactive protein level, gamma-glutamyltransferase level and neutrophil-to-lymphocyte ratio were identified as favourable prognostic factors for OS. Conclusions A selected subset of patients with advanced UC may experience long-term clinical benefit from anti-PD-(L)1 treatment. We identified prognostic factors that might be used for risk assessment and clinical trial stratification.
dc.language.isoeng
dc.publisherSpringer Nature
dc.relation.ispartofseriesBJC Reports;2
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectAparell genitourinari - Càncer - Immunoteràpia
dc.subjectAparell genitourinari - Prognosi
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshUrologic Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshAntibodies, Monoclonal
dc.subject.mesh/therapeutic use
dc.subject.meshProgression-Free Survival
dc.titleLong-term survival following anti-PD-(L)1 monotherapy in advanced urothelial cancer and an assessment of potential prognostic clinical factors: a multicentre observational study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1038/s44276-024-00104-3
dc.subject.decsneoplasias urológicas
dc.subject.decs/farmacoterapia
dc.subject.decsanticuerpos monoclonales
dc.subject.decs/uso terapéutico
dc.subject.decssupervivencia libre de progresión
dc.relation.publishversionhttps://doi.org/10.1038/s44276-024-00104-3
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Stockem CF] Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands. [Einerhand SMH] Department of surgical oncology (urology), The Netherlands Cancer Institute, Amsterdam, The Netherlands. [Miras Rodríguez I] Department of Medical Oncology, Hospital Universitario Virgen del Rocio, Seville, Spain. [Salhi Y] Department of Medical Oncology, Erasmus Medical Center, Rotterdam, The Netherlands. [Pérez E] Department of Medical Oncology, Hospital Complex Insular-Materno Infantil, Las Palmas, Spain. [Bakaloudi DR] Department of Medicine, Division of Hematology and Oncology, University of Washington, Seattle, USA. [Morales-Barrera R, Carles J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid39516359
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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