Safety of angiotensin converting enzyme inhibitors (ACEis) and angiotensin receptor blockers (ARBs) in patients with bladder and upper tract malignancies undergoing platinum-based chemotherapy: A retrospective study.

S Spencer Gibson (UCI Health, Orange, CA) D Dalia Kaakour (Division of Hematology and Oncology, University of California, Irvine, Orange, CA) O Omid Yazdanpanah B Benjamin J. Lee (37Department of Pharmacy, Chao Family Comprehensive Cancer Center, University of California Irvine Health, Orange, CA) N Nazmul Hasan (Department of Electrical and Computer Engineering, University of Rochester 1 , Rochester, New York 14627,) G Garo Greg Hagopian (Division of Medicine, University of California, Irvine, Orange, CA) B Brian Warnecke (Department of Hematology/Oncology, University of California Irvine Medical Center, Orange, CA) D Desiree Rafizadeh (UC Irvine School of Medicine, Irvine, CA) E Eva Zhao (UCI School of Medicine, Irvine, CA) G Garrett Harada (The Chao Family Comprehensive Cancer Center, Orange, CA) S Steven Neema Seyedin (University of California San Francisco, San Francisco, CA) A Arash Rezazadeh (Division of Hematology and Oncology, University of California, Irvine, Irvine, CA) N Nataliya Mar (University of California Irvine, Irvine, CA)

Abstract

e16563 Background: ACEis and ARBs are commonly used in the management of hypertension and cardiovascular disease, but little is known about their safety and impact on renal clearance when used in patients with bladder and upper tract malignancies receiving platinum-based chemotherapy (PBC). Methods: We performed an IRB-approved retrospective analysis of patients with bladder and upper tract malignancies at the University of California, Irvine, who received PBC between November 2017 and July 2023. Patients were grouped into cohort 1 (PBC + ACEis/ARBs) and cohort 2 (PBC without ACEis/ARBs). We used Chi-square tests for categorical variables and Student’s t-tests for continuous variables, with logistic regression to identify independent risk factors. Results: A total of 145 patients (mean age: 70) were included, with 47/145 (32%) receiving ACEis/ARBs at chemotherapy initiation. 64/145 (44%) were treated for metastatic disease and 11/145 (7.6%) received chemoradiation. Cisplatin was given to 84/145 (57.9%), carboplatin to 58/145 (40%). While chemotherapy regimen modifications (dose reductions, delays, cessations) were more frequent in cohort 1, the difference was not statistically significant (66% vs. 51%, P = 0.09). Independent risk factors associated with any regimen alterations included older age (in years) (aOR, 1.06; 95% CI, 1.02 to 1.10; P = 0.001) and receipt of carboplatin (aOR, 2.11; 95% CI, 1.01 to 4.40; P = 0.046). Chemotherapy-induced cytopenia was found in 32/47 (68.1%) of patients in cohort 1 vs. (56/98) 57.1% of patients in cohort 2, P = 0.21). No significant differences in acute kidney injury (P = 0.57) or hospitalization rates (P = 0.18) were observed. In multivariable logistic regression analysis, older age (aOR, 1.09; 95% CI, 1.05 to 1.14; P < 0.001) and metastatic disease (aOR, 2.41; 95% CI, 1.08 to 5.35; P = 0.031) were associated with any cytopenia or AKI. Conclusions: Concurrent use of ACEis/ARBs in bladder and upper tract cancer patients receiving PBC was associated with trends toward higher chemotherapy-induced toxicities and treatment alterations, though these findings were not statistically significant. Older age and metastatic disease were associated with cytopenias or AKI. These trends are worth exploring further in larger studies to ensure patient safety and treatment efficacy.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

S

Spencer Gibson

UCI Health, Orange, CA

D

Dalia Kaakour

Division of Hematology and Oncology, University of California, Irvine, Orange, CA

O

Omid Yazdanpanah

B

Benjamin J. Lee

37Department of Pharmacy, Chao Family Comprehensive Cancer Center, University of California Irvine Health, Orange, CA

N

Nazmul Hasan

Department of Electrical and Computer Engineering, University of Rochester 1 , Rochester, New York 14627,

G

Garo Greg Hagopian

Division of Medicine, University of California, Irvine, Orange, CA

B

Brian Warnecke

Department of Hematology/Oncology, University of California Irvine Medical Center, Orange, CA

D

Desiree Rafizadeh

UC Irvine School of Medicine, Irvine, CA

E

Eva Zhao

UCI School of Medicine, Irvine, CA

G

Garrett Harada

The Chao Family Comprehensive Cancer Center, Orange, CA

S

Steven Neema Seyedin

University of California San Francisco, San Francisco, CA

A

Arash Rezazadeh

Division of Hematology and Oncology, University of California, Irvine, Irvine, CA

N

Nataliya Mar

University of California Irvine, Irvine, CA