Update on the nephrotoxicity of novel anticancer agents

被引:9
|
作者
Nussbaum, Eliezer Zachary [1 ]
Perazella, Mark A. [2 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Med, Nephrol Sect, New Haven, CT 06520 USA
[3] VA Med Ctr, West Haven, CT USA
关键词
immunotherapy; nephrotoxicity; acute kidney injury; immune checkpoint inhibitors; interferon; angiogenesis inhibitors; CAR T-cells; RENAL-CELL CARCINOMA; ACUTE KIDNEY INJURY; ACUTE INTERSTITIAL NEPHRITIS; HIGH-DOSE INTERLEUKIN-2; GROWTH-FACTOR VEGF; RECEPTOR T-CELLS; THROMBOTIC MICROANGIOPATHY; TARGETED THERAPIES; INHIBITOR THERAPY; BRAF INHIBITORS;
D O I
10.5414/CN109371
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
Anticancer drug-induced kidney disease is a problem commonly encountered by nephrologists. The number of medications employed by oncologists causing acute and chronic kidney injury as well as electrolyte and acid-base disturbances has increased significantly over the past several decades. While conventional chemotherapeutic drugs induce a number of kidney lesions, emergence of very effective and well-tolerated targeted therapies and novel immunotherapies has increased the occurrence of drug-induced acute and chronic kidney injury in cancer patients. This article will review the various kidney lesions observed with these new classes of anticancer drugs.
引用
收藏
页码:149 / 165
页数:17
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