Abstract
Insulin-dependent diabetes may occur in patients with cancers who are treated with checkpoint inhibitors (CPIs). We reviewed 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.
© 2018 by the American Diabetes Association.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Antineoplastic Agents, Immunological / adverse effects*
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Antineoplastic Agents, Immunological / therapeutic use
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Autoimmune Diseases / chemically induced*
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Autoimmune Diseases / immunology
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Autoimmune Diseases / metabolism
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Autoimmune Diseases / physiopathology
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B7-H1 Antigen / antagonists & inhibitors*
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B7-H1 Antigen / metabolism
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Diabetes Mellitus, Type 1 / blood
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Diabetes Mellitus, Type 1 / drug therapy
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Diabetes Mellitus, Type 1 / etiology*
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Diabetes Mellitus, Type 1 / genetics
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Genetic Predisposition to Disease
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Genotype
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HLA-DR4 Antigen / blood
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HLA-DR4 Antigen / genetics
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HLA-DR4 Antigen / metabolism
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Humans
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Hypoglycemic Agents / therapeutic use
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Insulin / metabolism
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Insulin / therapeutic use
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Insulin Secretion
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Isoantibodies / analysis
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Ketosis / etiology
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Ketosis / prevention & control
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Models, Immunological*
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Neoplasms / drug therapy
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Neoplasms / metabolism
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Pancreas / drug effects
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Pancreas / immunology
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Pancreas / metabolism
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Pancreatitis / chemically induced*
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Pancreatitis / immunology
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Pancreatitis / metabolism
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Pancreatitis / physiopathology
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Programmed Cell Death 1 Receptor / antagonists & inhibitors*
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Programmed Cell Death 1 Receptor / metabolism
Substances
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Antineoplastic Agents, Immunological
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B7-H1 Antigen
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CD274 protein, human
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HLA-DR4 Antigen
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Hypoglycemic Agents
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Insulin
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Isoantibodies
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PDCD1 protein, human
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Programmed Cell Death 1 Receptor