Collateral Damage: Insulin-Dependent Diabetes Induced With Checkpoint Inhibitors

被引:431
作者
Stamatouli, Angeliki [1 ]
Quandt, Zoe [2 ]
Perdigoto, Ana Luisa [1 ]
Clark, Pamela L. [3 ]
Kluger, Harriet [4 ]
Weiss, Sarah A. [4 ]
Gettinger, Scott [4 ]
Sznol, Mario [4 ]
Young, Arabella [2 ]
Rushakoff, Robert [2 ]
Lee, James [5 ]
Bluestone, Jeffrey A. [2 ,6 ]
Anderson, Mark [2 ]
Herold, Kevan C. [1 ,3 ]
机构
[1] Yale Univ, Sect Endocrinol & Metab, Dept Internal Med, New Haven, CT 06520 USA
[2] Univ Calif San Francisco, Dept Med, Div Endocrinol & Metab, San Francisco, CA USA
[3] Yale Univ, Dept Immunobiol, New Haven, CT 06520 USA
[4] Yale Univ, Sect Med Oncol, Dept Internal Med, New Haven, CT USA
[5] Univ Calif San Francisco, Div Hematol & Oncol, San Francisco, CA 94143 USA
[6] Parker Inst Canc Immunotherapy, San Francisco, CA USA
关键词
ADVERSE EVENTS; AUTOIMMUNE; ENDOCRINE; THERAPY; CTLA-4; IMMUNOTHERAPY; ANTIBODIES; ANTI-PD-1; KETOACIDOSIS; DISORDERS;
D O I
10.2337/dbi18-0002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin-dependent diabetes may occur in patients with cancers who are treated with checkpoint inhibitors (CPIs). Wereviewed cases occurring over a 6-year period at two academic institutions and identified 27 patients in whom this developed, or an incidence of 0.9%. The patients had a variety of solid-organ cancers, but all had received either anti-PD-1 or anti-PD-L1 antibodies. Diabetes presented with ketoacidosis in 59%, and 42% had evidence of pancreatitis in the peridiagnosis period. Forty percent had at least one positive autoantibody and 21% had two or more. There was a predominance of HLA-DR4, which was present in 76% of patients. Other immune adverse events were seen in 70%, and endocrine adverse events in 44%. We conclude that autoimmune, insulin-dependent diabetes occurs in close to 1% of patients treated with anti-PD-1 or -PD-L1 CPIs. This syndrome has similarities and differences compared with classic type 1 diabetes. The dominance of HLA-DR4 suggests an opportunity to identify those at highest risk of these complications and to discover insights into the mechanisms of this adverse event.
引用
收藏
页码:1471 / 1480
页数:10
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