Rheumatic diseases associated with immune checkpoint inhibitors in cancer immunotherapy

被引:10
|
作者
Ohnuma, Kei [1 ]
Hatano, Ryo [1 ]
Dang, Nam H. [2 ]
Morimoto, Chikao [1 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Therapy Dev & Innovat Immune Disorders & Can, Tokyo, Japan
[2] Univ Florida, Div Hematol Oncol, Gainesville, FL USA
关键词
Immune checkpoint inhibitor; immune-related adverse events; inflammatory arthritis; rheumatic disease; ADVERSE EVENTS; INFLAMMATORY ARTHRITIS; ADVANCED MELANOMA; MOLECULAR-MECHANISMS; IPILIMUMAB THERAPY; T-CELLS; PD-1; CTLA-4; DYSFUNCTION; NIVOLUMAB;
D O I
10.1080/14397595.2018.1532559
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immune checkpoint inhibitors (ICIs) have drastically altered cancer treatment paradigms, with increasing numbers of novel ICIs being currently evaluated in numerous clinical trials for various cancers. ICIs release 'brakes' against tumor immunity to control cancer growth through T cell-dependent anti-tumor activity. Meanwhile, side effects associated with ICIs are directly related to their mechanism of action, as nonspecific immune activation targeting non-tumor organs results in undesirable off-target inflammation and autoimmunity. Accumulating data reveal that immune-related adverse events (irAEs) of ICIs in cancer patients can resemble various rheumatic diseases. Moreover, while patients with preexisting rheumatic diseases can theoretically experience irAEs and disease flares, observational studies have shown that ICIs can be used successfully in these patients. As ICIs continue to provide long-lasting disease control in cancer patients and their usage correspondingly increases, the rheumatologist will be managing new ICI-associated clinical entities mimicking common autoimmune diseases and will need to be prepared to rapidly diagnose and treat these irAEs. Early recognition and treatment of these rheumatic adverse events will allow for improved outcomes and quality of life for cancer patients faced with previously rapidly fatal disease.
引用
收藏
页码:721 / 732
页数:12
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