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.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] Immune checkpoint inhibitor-associated acute kidney injury in patients with cancer: a systematic review and meta-analysis of risk factors
    Yan, Haoyu
    Tang, Meimei
    Zhu, Wei
    Yang, Yiqun
    CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2023, 27 (07) : 603 - 612
  • [32] Immune checkpoint inhibitor-associated acute kidney injury in patients with cancer: a systematic review and meta-analysis of risk factors
    Haoyu Yan
    Meimei Tang
    Wei Zhu
    Yiqun Yang
    Clinical and Experimental Nephrology, 2023, 27 : 603 - 612
  • [33] Clinical characteristics, time course, treatment and outcomes of patients with immune checkpoint inhibitor-associated myocarditis
    Puzanov, Igor
    Subramanian, Poornima
    Yatsynovich, Yan, V
    Jacobs, David M.
    Chilbert, Maya R.
    Sharma, Umesh C.
    Ito, Fumito
    Feuerstein, Steven G.
    Stefanovic, Filip
    Switzer, Benjamin
    Hicar, Mark D.
    Curtis, Anne B.
    Spangenthal, Edward J.
    Dy, Grace K.
    Ernstoff, Marc S.
    Vachhani, Pankit
    Page, Brian J.
    Agrawal, Nikhil
    Khunger, Arjun
    Kapoor, Ankita
    Hattoum, Alexander
    Jerome, Schentag J.
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 (06)
  • [34] Recent advances in the study of immune checkpoint inhibitor-associated pneumonia
    Feng, Xiaoan
    Li, Guohui
    Li, Chunyu
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2025, 206
  • [35] IMMUNE CHECKPOINT INHIBITOR-ASSOCIATED CELIAC DISEASE
    Badran, Yousef R.
    Shih, Angela
    Leet, Donna
    Coromilas, Alexandra
    Chen, Jonathan
    Kem, Marina
    Borowsky, Jennifer
    Misdraji, Joseph
    Mino-Kenudson, Mari
    Dougan, Michael
    GASTROENTEROLOGY, 2020, 158 (06) : S156 - S156
  • [36] Immune Checkpoint Inhibitor-Associated Autoimmune Encephalitis
    Yordduangjun, Nichakarn
    Dishion, Evan
    McKnight, Curtis A.
    Caplan, Jason P.
    JOURNAL OF THE ACADEMY OF CONSULTATION-LIAISON PSYCHIATRY, 2021, 62 (01): : 115 - 118
  • [37] Update on Immune Checkpoint Inhibitor-Associated Uveitis
    Christian Kim
    Samantha Paul
    Jose Echegaray
    Current Ophthalmology Reports, 2023, 11 : 57 - 67
  • [38] Reconceptualization of immune checkpoint inhibitor-associated gastritis
    Deng, Ying-Fang
    Cui, Xian-Shu
    Wang, Liang
    WORLD JOURNAL OF GASTROENTEROLOGY, 2024, 30 (36)
  • [39] Immune checkpoint inhibitor-associated celiac disease
    Badran, Yousef
    Shih, Angela
    Leet, Donna
    Mooradian, Meghan J.
    Coromilas, Alexandra
    Chen, Jonathan
    Kem, Marina
    Zheng, Hui
    Borowsky, Jennifer
    Misdraji, Joseph
    Mino-Kenudson, Mari
    Dougan, Michael
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2020, 8 (01)
  • [40] A Case of Immune Checkpoint Inhibitor-Associated Gastritis
    Mansour, Mahmoud
    Abudalou, Mohammad
    Nale, Hanna
    Rao, Deepthi
    Hammoud, Ghassan
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2024, 119 (10S): : S3136 - S3136