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

被引:0
|
作者
Yang, Ting-Ya [1 ]
Chuang, Min-Hsiang [2 ]
Lin, Hong-Min [1 ]
Wu, Vin-Cent [3 ]
Pan, Heng-Chih [4 ]
Chou, Yun [5 ,6 ]
Chen, Jui-Yi [2 ,7 ]
机构
[1] Chi Mei Med Ctr, Dept Family Med, Tainan, Taiwan
[2] Chi Mei Med Ctr, Dept Internal Med, Div Nephrol, Tainan, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[4] Keelung Chang Gung Mem Hosp, Dept Internal Med, Keelung, Taiwan
[5] Chi Mei Med Ctr, Dept Pediat, Tainan, Taiwan
[6] Shu Zen Jr Coll Med & Management, Dept Early Childhood Care & Educ, Kaohsiung, Taiwan
[7] Chia Nan Univ Pharm & Sci, Dept Hlth & Nutr, Tainan, Taiwan
来源
BMJ OPEN | 2025年 / 15卷 / 02期
关键词
ONCOLOGY; IMMUNOLOGY; NEPHROLOGY; Acute renal failure; ADVERSE EVENTS;
D O I
10.1136/bmjopen-2024-092752
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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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页数:9
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