Publication: Immune checkpoint blockade therapies efficacy and toxicity in patients with impaired renal function in metastatic bladder cancer
dc.contributor.coauthor | Arslan, Cagatay | |
dc.contributor.coauthor | Olmez, Omer Fatih | |
dc.contributor.coauthor | Erman, Mustafa | |
dc.contributor.coauthor | Urun, Yueksel | |
dc.contributor.coauthor | Erdem, Dilek | |
dc.contributor.coauthor | Kilickap, Saadettin | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Tural, Deniz | |
dc.contributor.kuauthor | Selçukbiricik, Fatih | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2025-03-06T20:57:47Z | |
dc.date.issued | 2024 | |
dc.description.abstract | Background: In this study, we reported the real-life results of data from impaired renal patients with urothelial carcinoma who were treated with ICTs. Methods: The patients were categorized into 3 different groups GFR >= 60mL/min (normal), 60mL/min-30mL/min (low), and less than 30 mL/min (very low) based on GFR. The primary endpoints were the overall response rate (ORR), overall survival (OS), duration of response with ICT, and safety. Median follow-up and OS were estimated by using the Kaplan-Meier method. Results: One hundred-five (60.3%) of patients were GFR normal, 26.4% were GFR low with 30mL/min-60mL/min, and 13.2% were very low group. ORR for GFR normal, low and very low groups were 36% ( n = 38), 26% ( n = 12) and %31 (7);P = .2, respectively. The median duration of response for GFR normal, low and very low groups were 47.2 months (95% CI, 24.5-51.4), 33.1 months (95% CI, 26.9-47), and 23.5 months (95% CI, 12.2-43.7);P = .01, respectively. The Median OS rate for GFR normal, low and very low groups were 11.9 (7.2-16.5) months, 4.7 (1.8-7.7) and 6.8 (1.1-13.6) months, P = .015, respectively. In addition, GFR < 60 ml/min HR = 1.6;95% CI1.12-1.80;P = .02, maintained a significant association with OS in multivariate analysis. Conclusions: Long-term follow-up of real-world data confirms that the overall survival rate and durable response rate with ICT were higher in patients with GFR >60mL/min. On the other hand, we demonstrated that ICT was effective and a durable response seen in a group of patients with renal inpairement who did not have an effective systemic treatment option. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.identifier.doi | 10.1016/j.clgc.2024.102228 | |
dc.identifier.eissn | 1938-0682 | |
dc.identifier.issn | 1558-7673 | |
dc.identifier.issue | 6 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-85207147913 | |
dc.identifier.uri | https://doi.org/10.1016/j.clgc.2024.102228 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/27313 | |
dc.identifier.volume | 22 | |
dc.identifier.wos | 1347208300001 | |
dc.keywords | Immune checkpoint blockade therapies | |
dc.keywords | Urothelial carcinoma | |
dc.keywords | Renal failure | |
dc.keywords | Long term follow up | |
dc.keywords | Outcomes | |
dc.language.iso | eng | |
dc.publisher | CIG Media Group, LP | |
dc.relation.ispartof | CLINICAL GENITOURINARY CANCER | |
dc.subject | Oncology | |
dc.subject | Urology | |
dc.subject | Nephrology | |
dc.title | Immune checkpoint blockade therapies efficacy and toxicity in patients with impaired renal function in metastatic bladder cancer | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Tural, Deniz | |
local.contributor.kuauthor | Selçukbiricik, Fatih | |
local.contributor.kuauthor | Akar, Emre | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
relation.isParentOrgUnitOfPublication.latestForDiscovery | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e |
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