Kidney Complications of Immune Checkpoint Inhibitors: A Review

被引:49
作者
Shingarev, Roman [1 ,2 ]
Glezerman, Ilya G. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10065 USA
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
ACUTE INTERSTITIAL NEPHRITIS; LONG-TERM SURVIVAL; ADVERSE EVENTS; ADVANCED MELANOMA; POOLED ANALYSIS; CELL CARCINOMA; T-CELLS; IPILIMUMAB; NIVOLUMAB; CANCER;
D O I
10.1053/j.ajkd.2019.03.433
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
Immunologic control of malignancy has long been recognized as an important determinant of disease progression. Recent advances in immunology have led to the focus on several mechanisms that can be targeted to achieve tumor suppression. In particular, checkpoint inhibition has evolved in less than a decade to become one of the most important strategies in cancer therapy, with a meaningful improvement in patient survival. Six agents have been approved for clinical use to date and many more are in the industry pipeline. The spectrum of malignancies responsive to immunotherapy ranges from advanced melanoma, for which the first immune checkpoint inhibitor ipilimumab was approved, to Hodgkin lymphoma, non-small cell lung cancer, renal cell carcinoma, and others. Notwithstanding its clinical benefits, checkpoint inhibition carries a risk for significant off-target toxicity stemming from the immune system activation. In this review, we discuss general principles of checkpoint inhibition, mechanisms of toxicity, and kidney complications of the treatment and propose diagnostic and treatment strategies when kidney injury occurs.
引用
收藏
页码:529 / 537
页数:9
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