Clinical outcomes after immune checkpoint inhibitor-associated acute kidney injury: a cohort study

医学 急性肾损伤 队列研究 队列 流行病学 内科学 肿瘤科 重症监护医学
作者
Ting-Ya Yang,Min‐Hsiang Chuang,Hong-Min Lin,Vin‐Cent Wu,Heng‐Chih Pan,Y.‐J. Chou,Jui‐Yi Chen
出处
期刊:BMJ Open [BMJ]
卷期号:15 (2): e092752-e092752 被引量:2
标识
DOI:10.1136/bmjopen-2024-092752
摘要

OBJECTIVES: Immune checkpoint inhibitors (ICPi) have significantly improved survival for patients with advanced cancers. However, the occurrence of ICPi-associated acute kidney injury (AKI) and its clinical impact remains unclear. This study evaluates the effects of ICPi-associated AKI (ICPi-AKI) on mortality, kidney and cardiovascular outcomes in patients undergoing ICPi treatments. DESIGN: This multicentre retrospective cohort study with propensity score matching to balance baseline characteristics. The International Classification of Diseases, 10th Revision codes were used to identify individuals with cancer and treated with ICPi concurrently. Kaplan-Meier analyses coupled with log-rank tests were conducted to estimate the survival probabilities. SETTING: Data were sourced from the TriNetX database spanning records from 25 March 2011 to 5 April 2024. PARTICIPANTS: Patients with cancer aged ≥18 years treated with ICPi with or without AKI occurrence. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome was all-cause mortality, and secondary outcomes included major adverse kidney events (MAKE), major adverse cardiovascular events (MACE), the composite of MAKE or MACE with death, and end-stage renal disease. RESULTS: The study identified 926 patients with cancer who developed ICPi-AKI (mean age, 67.1±11.8 years; 57.4% men). The control group consisted of 48 147 patients treated with ICPi but did not develop AKI (mean age, 65.3±13.1 years; 53.7% men). After matching, the ICPi-AKI group exhibited a higher risk of all-cause mortality (HR=1.27; 95% CI 1.02 to 1.61), MAKE (HR=3.83; 95% CI 1.72 to 8.40), MACE (HR=1.35; 95% CI 1.03 to 1.75)) compared with the non-ICPi-AKI group. Subgroup analyses confirmed these findings across various patient's characteristics. CONCLUSION: Individuals with ICPi-AKI are associated with an increased risk of all-cause mortality, MAKE and MACE. Enhancing awareness and timely intervention for ICPi-AKI are crucial for improving prognosis and reducing complications among patients with cancer.
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