Immune Checkpoint Inhibitor–Associated Acute Kidney Injury

医学 急性肾损伤 免疫抑制 肾脏疾病 肾癌 重症监护医学 不利影响 狼疮性肾炎 内科学 疾病 癌症 舒尼替尼 观察研究 肾病科 易普利姆玛 梅德林 肿瘤科 肾 活检 硫唑嘌呤 指南 免疫学 病理
作者
Shruti Gupta,Roberta Fenoglio,Naoka Murakami,Elad Sharon,Sandra M. Herrmann,Biruh Workeneh,Dario Roccatello,Jack A. Blau,Marlies Ostermann,Claudio Ronco,Amanda D. Renaghan,Mitchell Howard Rosner,David E. Leaf,on behalf of the ADQI Conference Participants
出处
期刊:Journal of The American Society of Nephrology [American Society of Nephrology]
卷期号:37 (10): 2329-2344 被引量:1
标识
DOI:10.1681/asn.0000001232
摘要

Immune checkpoint inhibitors (ICIs) have transformed cancer therapy but are associated with immune-related adverse events, including ICI-associated AKI (ICI-AKI). ICI-AKI presents diagnostic and management challenges and can influence decisions regarding immunosuppression and ICI rechallenge, with important implications for both kidney and cancer outcomes. An international, multidisciplinary panel convened at the 34th Acute Disease Quality Initiative (ADQI) consensus conference in September 2024. Systematic literature searches of PubMed were conducted to identify studies on the epidemiology, mechanisms, diagnosis, management, rechallenge, and outcomes of ICI-AKI. The meeting followed the established ADQI process and used a modified Delphi method to achieve consensus. Evidence was reviewed and appraised by workgroups, and consensus statements were developed through structured discussion and voting. Observational data suggest that AKI occurs in up to 20% of patients receiving ICIs, with ICI-AKI accounting for approximately 2%-5% of cases. Acute tubulointerstitial nephritis is the most common lesion, observed in 80%-90% of biopsies, although glomerular diseases are increasingly recognized. No clinical features reliably distinguish ICI-AKI from other causes of AKI, and kidney biopsy remains the diagnostic gold standard. Emerging urinary, circulating, and imaging biomarkers show promise but are not yet ready for routine clinical use. Early glucocorticoid initiation (within 3 days of ICI-AKI diagnosis versus >3 days after diagnosis) is associated with higher rates of kidney recovery, although optimal dosing and duration remain uncertain. Recurrent ICI-AKI occurs in fewer than 20% of patients undergoing ICI rechallenge. Management of high-risk populations, including kidney transplant recipients and patients with autoimmune disease or advanced CKD, requires individualized, multidisciplinary decision making. ICI-AKI is an important and potentially reversible complication of cancer immunotherapy; these consensus statements provide a framework for diagnosis and management, support cautious ICI rechallenge in selected patients, and identify priorities for future research.
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