A review of cancer immunotherapy toxicity

被引:1352
作者
Kennedy, Lucy Boyce [1 ]
Salama, April K. S. [2 ]
机构
[1] Duke Univ, Hematol Oncol, Durham, NC 27710 USA
[2] Duke Univ, Div Med Oncol, Durham, NC 27710 USA
关键词
checkpoint inhibitor; chimeric antigen receptor (CAR) T cells; cytokine release syndrome; cytotoxic T-lymphocyte antigen 4 (CTLA-4); immune effector cell-associated neurotoxicity syndrome (ICANS); immune-related adverse events (irAEs); programmed cell death protein 1 (PD-1); IMMUNE CHECKPOINT INHIBITORS; T-CELL THERAPY; NIVOLUMAB PLUS IPILIMUMAB; ADVERSE EVENTS; ADVANCED MELANOMA; STAGE-III; DEATH; B-CELL; METASTATIC MELANOMA; TREATMENT FAILURE;
D O I
10.3322/caac.21596
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cancer immunotherapies, including checkpoint inhibitors and adoptive cell therapy, manipulate the immune system to recognize and attack cancer cells. These therapies have the potential to induce durable responses in multiple solid and hematologic malignancies and thus have transformed treatment algorithms for numerous tumor types. Cancer immunotherapies lead to unique toxicity profiles distinct from the toxicities of other cancer therapies, depending on their mechanism of action. These toxicities often require specific management, which can include steroids and immune-modulating therapy and for which consensus guidelines have been published. This review will focus on the toxicities of checkpoint inhibitors and chimeric antigen receptor T cells, including pathophysiology, diagnosis, and management.
引用
收藏
页码:86 / 104
页数:19
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