Cargando…
Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study
Clinical trials revealed significant antitumor activity for immune checkpoint inhibitors (ICI) in metastatic urothelial carcinoma (mUC). Due to their strict eligibility criteria, clinical trials include selected patient cohorts, and thus do not necessarily represent real-world population outcomes. I...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575904/ https://www.ncbi.nlm.nih.gov/pubmed/37833455 http://dx.doi.org/10.1038/s41598-023-44103-9 |
_version_ | 1785121010804064256 |
---|---|
author | Váradi, Melinda Horváth, Orsolya Módos, Orsolya Fazekas, Tamás Grunewald, Camilla M. Niegisch, Günter Krafft, Ulrich Grünwald, Viktor Hadaschik, Boris Olah, Csilla Maráz, Anikó Furka, Andrea Szűcs, Miklós Nyirády, Péter Szarvas, Tibor |
author_facet | Váradi, Melinda Horváth, Orsolya Módos, Orsolya Fazekas, Tamás Grunewald, Camilla M. Niegisch, Günter Krafft, Ulrich Grünwald, Viktor Hadaschik, Boris Olah, Csilla Maráz, Anikó Furka, Andrea Szűcs, Miklós Nyirády, Péter Szarvas, Tibor |
author_sort | Váradi, Melinda |
collection | PubMed |
description | Clinical trials revealed significant antitumor activity for immune checkpoint inhibitors (ICI) in metastatic urothelial carcinoma (mUC). Due to their strict eligibility criteria, clinical trials include selected patient cohorts, and thus do not necessarily represent real-world population outcomes. In this multicentric, retrospective study, we investigated real-world data to assess the effectiveness of pembrolizumab and atezolizumab and to evaluate the prognostic value of routinely available clinicopathological and laboratory parameters. Clinical and follow-up data from mUC patients who received ICIs (01/2017-12/2021) were evaluated. Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and duration of response (DOR) were used as endpoints. Patients’ (n = 210, n = 76 atezolizumab and 134 pembrolizumab) median OS and PFS were 13.6 and 5.9 months, respectively. Impaired ECOG-PS, the presence of visceral, liver or bone metastases, and hemoglobin levels were independently associated with poor OS and DCR. Furthermore, Bellmunt risk factors and the enhanced Bellmunt-CRP score were shown to be prognostic for OS, PFS and DCR. In conclusion, ICIs are effective treatments for a broad range of mUC patients. Our results confirmed the prognostic value of numerous risk factors and showed that Bellmunt risk scores can further be improved when adding CRP to the model. |
format | Online Article Text |
id | pubmed-10575904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105759042023-10-15 Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study Váradi, Melinda Horváth, Orsolya Módos, Orsolya Fazekas, Tamás Grunewald, Camilla M. Niegisch, Günter Krafft, Ulrich Grünwald, Viktor Hadaschik, Boris Olah, Csilla Maráz, Anikó Furka, Andrea Szűcs, Miklós Nyirády, Péter Szarvas, Tibor Sci Rep Article Clinical trials revealed significant antitumor activity for immune checkpoint inhibitors (ICI) in metastatic urothelial carcinoma (mUC). Due to their strict eligibility criteria, clinical trials include selected patient cohorts, and thus do not necessarily represent real-world population outcomes. In this multicentric, retrospective study, we investigated real-world data to assess the effectiveness of pembrolizumab and atezolizumab and to evaluate the prognostic value of routinely available clinicopathological and laboratory parameters. Clinical and follow-up data from mUC patients who received ICIs (01/2017-12/2021) were evaluated. Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and duration of response (DOR) were used as endpoints. Patients’ (n = 210, n = 76 atezolizumab and 134 pembrolizumab) median OS and PFS were 13.6 and 5.9 months, respectively. Impaired ECOG-PS, the presence of visceral, liver or bone metastases, and hemoglobin levels were independently associated with poor OS and DCR. Furthermore, Bellmunt risk factors and the enhanced Bellmunt-CRP score were shown to be prognostic for OS, PFS and DCR. In conclusion, ICIs are effective treatments for a broad range of mUC patients. Our results confirmed the prognostic value of numerous risk factors and showed that Bellmunt risk scores can further be improved when adding CRP to the model. Nature Publishing Group UK 2023-10-13 /pmc/articles/PMC10575904/ /pubmed/37833455 http://dx.doi.org/10.1038/s41598-023-44103-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Váradi, Melinda Horváth, Orsolya Módos, Orsolya Fazekas, Tamás Grunewald, Camilla M. Niegisch, Günter Krafft, Ulrich Grünwald, Viktor Hadaschik, Boris Olah, Csilla Maráz, Anikó Furka, Andrea Szűcs, Miklós Nyirády, Péter Szarvas, Tibor Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title | Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title_full | Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title_fullStr | Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title_full_unstemmed | Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title_short | Efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
title_sort | efficacy of immune checkpoint inhibitor therapy for advanced urothelial carcinoma in real-life clinical practice: results of a multicentric, retrospective study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575904/ https://www.ncbi.nlm.nih.gov/pubmed/37833455 http://dx.doi.org/10.1038/s41598-023-44103-9 |
work_keys_str_mv | AT varadimelinda efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT horvathorsolya efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT modosorsolya efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT fazekastamas efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT grunewaldcamillam efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT niegischgunter efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT krafftulrich efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT grunwaldviktor efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT hadaschikboris efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT olahcsilla efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT marazaniko efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT furkaandrea efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT szucsmiklos efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT nyiradypeter efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy AT szarvastibor efficacyofimmunecheckpointinhibitortherapyforadvancedurothelialcarcinomainreallifeclinicalpracticeresultsofamulticentricretrospectivestudy |