Publication:
Immune checkpoints 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,Yuksel
dc.contributor.coauthorErdem,Dilek
dc.contributor.coauthorKilickap,Saadettin
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorSelçukbiricik, Fatih
dc.contributor.kuauthorTural, Deniz
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T20:59:01Z
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 immune checkpoint blockade therapies (ICT). Methods: This study included metastatic urothelial carcinoma patients treated with at least one course of ICT. Impaired renal function was defined as a glomerular filtration rate [GFR] less than 60 mL/min. The patients were categorized into 3 different groups GFR≥60mL/min (normal), 60–30mL/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 using the Kaplan-Meier method. Results: Data from 174 eligible patients were analyzed, 4% of these patients received the ICT as the first line, 83.3 % as the second line, and 12.7 % as the third or more line of treatment. One hundred-five( 60.3%) of patients were GFR normal, 26.4% were GFR low with 30–60 mL/min, and %13.2 were very low group. The median follow-up time was 52 (1.15–62) months. ORR for GFR normal, low, and very low groups were 36% (n=38), 26% (n=12), and %31 (7); p=0.2, 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=0.01, 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=0.015, respectively. In univariate analysis, liver metastases, baseline creatinine clearance less (GFR) than 60 ml/min, ECOG PS (1 ≥), and hemoglobin levels < 10 mg/dl were all significantly associated with OS. Three of the adverse prognostic factors according to the Bellmunt criteria were independent of short survival: liver metastases HR=1.6; 95% CI 1.02-3.52; p= 0.043), ECOG PS (1 ≥) HR=2.3; 95% CI 11.05-2.44; p=0.029), and hemoglobin level < 10 mg/dl HR=1.5; 95% CI 1.07-2.34; p: 0.021). In addition, GFR <60 ml/min HR=1.6; 95% CI 1.12-1.80; p=0.02, maintained a significant association with OS in multivariate analysis. GFR normal, low, and very low groups experienced %62.9, 54.3%, and 43.5% of treatment-related adverse events of any grade, respectively. There are no significant differences among each group(p=0.2). Also, treatment-related death and discontinuation were insignificant among each group. 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 long durable response was seen in a group of patients with renal impairment who did not have an effective systemic treatment option, The safety profile was consistent with prior reports and similar in each group.
dc.description.indexedbyWOS
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1200/JCO.2024.42.4_suppl.594
dc.identifier.eissn1527-7755
dc.identifier.issn0732-183X
dc.identifier.issue4_SUPPL
dc.identifier.quartileQ1
dc.identifier.urihttps://doi.org/10.1200/JCO.2024.42.4_suppl.594
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27612
dc.identifier.volume42
dc.identifier.wos1266676900112
dc.keywords3282-4644-2702-2534
dc.keywords613-135-2370-7650-2700
dc.keywords261-492-2769
dc.keywords613-135-244-3829
dc.keywords283-2494
dc.keywords283-237-2581-242
dc.keywords3282-3306-4614-3660
dc.keywords11
dc.keywords5
dc.keywords2
dc.keywords2
dc.keywords2
dc.keywords2
dc.keywords2
dc.language.isoeng
dc.publisherLippincott Williams & Wilkins
dc.relation.ispartofJournal of Clinical Oncology
dc.subjectOncology
dc.titleImmune checkpoints blockade therapies' efficacy and toxicity in patients with impaired renal function in metastatic bladder cancer
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.kuauthorTural, Deniz
local.contributor.kuauthorSelçukbiricik, Fatih
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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