Renal effects of immune checkpoint inhibitors

被引:74
作者
Izzedine, Hassan [1 ]
Mateus, Christine [2 ]
Boutros, Celine [2 ]
Robert, Caroline [2 ]
Rouvier, Philippe [3 ]
Amoura, Zahir [4 ]
Mathian, Alexis
机构
[1] Monceau Pk Int Clin Paris, Dept Nephrol, Paris, France
[2] Gustave Roussy Inst, Dept Oncol, Villejuif, France
[3] Hop La Pitie Salpetriere, Dept Pathol, Paris, France
[4] Hop La Pitie Salpetriere, Dept Internal Med 2, Paris, France
关键词
checkpoint blockade; immunotherapy; ipilimumab; nivolumab; pembrolizumab; OVERCOMING IMMUNOLOGICAL-TOLERANCE; ACUTE INTERSTITIAL NEPHRITIS; MELANOMA TARGETING CTLA-4; ANTI-PD-1; ANTIBODY; PHASE-II; IPILIMUMAB; NIVOLUMAB; SAFETY; BLOCKADE; PEMBROLIZUMAB;
D O I
10.1093/ndt/gfw382
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Recent advances in immune checkpoint inhibitor (ICPI) development have led to major improvements in oncology patient outcomes. Cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed cell death protein 1 (PD-1) are two essential immune checkpoint receptors. Ipilimumab and tremelimumab (anti-CTLA-4-blocking antibodies) and pembrolizumab and nivolumab (antibodies targeting PD-1 receptors) have already been approved by US Food and Drug Administration in several malignancies. Two different forms of ICPI-induced renal damage have been identified, including acute (granulomatous) tubulointerstitial nephritis and immune complex glomerulonephritis. The observed acute renal damage can be reversed upon ICPI drug discontinuation and renal function can recover back to normal following the introduction of systemic corticosteroid treatment. Any delay in treating this complication could result in definitive and irreversible renal injury.
引用
收藏
页码:936 / 942
页数:7
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