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Immune checkpoint blockade therapies efficacy and toxicity in patients with impaired renal function in metastatic bladder cancer

dc.contributor.coauthorArslan, Cagatay
dc.contributor.coauthorOlmez, Omer Fatih
dc.contributor.coauthorErman, Mustafa
dc.contributor.coauthorUrun, Yueksel
dc.contributor.coauthorErdem, Dilek
dc.contributor.coauthorKilickap, Saadettin
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorTural, Deniz
dc.contributor.kuauthorSelçukbiricik, Fatih
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T20:57:47Z
dc.date.issued2024
dc.description.abstractBackground: 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.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1016/j.clgc.2024.102228
dc.identifier.eissn1938-0682
dc.identifier.issn1558-7673
dc.identifier.issue6
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85207147913
dc.identifier.urihttps://doi.org/10.1016/j.clgc.2024.102228
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27313
dc.identifier.volume22
dc.identifier.wos1347208300001
dc.keywordsImmune checkpoint blockade therapies
dc.keywordsUrothelial carcinoma
dc.keywordsRenal failure
dc.keywordsLong term follow up
dc.keywordsOutcomes
dc.language.isoeng
dc.publisherCIG Media Group, LP
dc.relation.ispartofCLINICAL GENITOURINARY CANCER
dc.subjectOncology
dc.subjectUrology
dc.subjectNephrology
dc.titleImmune checkpoint blockade therapies efficacy and toxicity in patients with impaired renal function in metastatic bladder cancer
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorTural, Deniz
local.contributor.kuauthorSelçukbiricik, Fatih
local.contributor.kuauthorAkar, Emre
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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