Acute Kidney Injury Induced by Immune Checkpoint Inhibitors

被引:11
作者
Tian, Ruixue [1 ]
Liang, Jin [1 ]
Li, Rongshan [2 ]
Zhou, Xiaoshuang [2 ]
机构
[1] Shanxi Med Univ, Clin Med Coll 5, Taiyuan, Peoples R China
[2] Shanxi Med Univ, Shanxi Prov Peoples Hosp, Shanxi Kidney Dis Inst, Clin Med Coll 5,Dept Nephrol, Taiyuan, Peoples R China
关键词
Acute kidney injury; Immune checkpoint inhibitors; Acute interstitial nephritis; Immune-related adverse events; ACUTE INTERSTITIAL NEPHRITIS; URINARY SOLUBLE CD163; NIVOLUMAB; THERAPY; ASSOCIATION; FEATURES; PROTEIN; PD-L1; CELLS; RISK;
D O I
10.1159/000520798
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Recent advances in immune therapy have focused on several agents that target tumor suppression; specifically, use of immune checkpoint inhibitors (ICIs), such as ipilimumab, pembrolizumab, and nivolumab, has become an important strategy in cancer therapy as they improve outcomes in malignant disease. However, the incidence of renal complications arising from the widespread use of ICIs may be underestimated. Summary: The most frequently reported renal condition caused by ICI use is acute interstitial nephritis, and for clinicians, the crucial question is how to effectively manage patients who develop renal side effects due to cancer treatment. Currently, treatment of kidney injury associated with ICIs adheres to clinical guidelines described in Kidney Disease Improving Global Outcomes, which entails drug withdrawal and glucocorticoids or combined immunosuppressant use based on disease stage; however, there is no consensus on renal biopsy. Key Messages: Despite significant progress in prevention and treatment, the incidence and mortality of ICI-induced acute kidney injury (AKI) remain very high. This article will discuss the general clinical manifestations, mechanisms of toxicity, renal complications of ICI therapy, and related biomarkers of renal damage. It is envisaged that this information would help clinicians effectively manage AKI due to ICI therapy.
引用
收藏
页码:190 / 201
页数:12
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