| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Stockem, Chantal F. |
| dc.contributor.author | Einerhand, Sarah M. H. |
| dc.contributor.author | Miras, Isabel |
| dc.contributor.author | Salhi, Youssra |
| dc.contributor.author | Pérez Calabuig, Esther |
| dc.contributor.author | Bakaloudi, Dimitra Rafailia |
| dc.contributor.author | Morales-Barrera, Rafael |
| dc.contributor.author | Carles, Joan |
| dc.date.accessioned | 2025-01-08T09:43:03Z |
| dc.date.available | 2025-01-08T09:43:03Z |
| dc.date.issued | 2024-10-23 |
| dc.identifier.citation | Stockem 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.issn | 2731-9377 |
| dc.identifier.uri | https://hdl.handle.net/11351/12378 |
| dc.description | Long-term survival; Monotherapy; Advanced urothelial cancer |
| dc.description.abstract | Background
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.iso | eng |
| dc.publisher | Springer Nature |
| dc.relation.ispartofseries | BJC Reports;2 |
| 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 | Anticossos monoclonals - Ús terapèutic |
| dc.subject | Aparell genitourinari - Càncer - Immunoteràpia |
| dc.subject | Aparell genitourinari - Prognosi |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject.mesh | Urologic Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Antibodies, Monoclonal |
| dc.subject.mesh | /therapeutic use |
| dc.subject.mesh | Progression-Free Survival |
| dc.title | 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 |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1038/s44276-024-00104-3 |
| dc.subject.decs | neoplasias urológicas |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | anticuerpos monoclonales |
| dc.subject.decs | /uso terapéutico |
| dc.subject.decs | supervivencia libre de progresión |
| dc.relation.publishversion | https://doi.org/10.1038/s44276-024-00104-3 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 39516359 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |