Anti-PD-L1 atezolizumab-Induced Autoimmune Diabetes: a Case Report and Review of the Literature

被引:42
作者
Hickmott, Laura [1 ]
De La Pena, Hugo [1 ]
Turner, Helen [2 ]
Ahmed, Fathelrahman [2 ]
Protheroe, Andrew [1 ]
Grossman, Ashley [2 ]
Gupta, Avinash [3 ]
机构
[1] Oxford Univ Hosp NHS Fdn Trust, Churchill Hosp, Dept Oncol, Oxford OX3 7LE, England
[2] Oxford Univ Hosp NHS Fdn Trust, Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LE, England
[3] Christie NHS Fdn Trust, Dept Med Oncol, Manchester M20 4BX, Lancs, England
关键词
CELL DEATH-1 THERAPY; ADVANCED MELANOMA; ADVERSE EVENTS; NOD MICE; CANCER; IMMUNOTHERAPY; NIVOLUMAB; FULMINANT; ANTIBODY; EXPRESSION;
D O I
10.1007/s11523-017-0480-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Programmed cell death-1 and programmed death ligand 1 (PD-1/PD-L1) inhibitors trigger an immune-mediated anti-tumour response by promoting the activation of cytotoxic T lymphocytes. Although proven to be highly effective in the treatment of several malignancies they can induce significant immune-related adverse events (irAEs) including endocrinopathies, most commonly hypophysitis and thyroid dysfunction, and rarely autoimmune diabetes. Here we present the first case report of a patient with a primary diagnosis of urothelial cancer developing PD-L1 inhibitor-induced autoimmune diabetes. A euglycemic 57 year old male presented to clinic with dehydration after the fifth cycle of treatment with the novel PD-L1 inhibitor atezolizumab. Blood tests demonstrated rapid onset hyperglycaemia (BM 24 mmol/L), ketosis and a low C-peptide level (0.65 ng/mL) confirming the diagnosis of type 1 diabetes. He responded well to insulin therapy and was discharged with stable blood glucose levels. Due to the widening use of PD-1/PD-L1 inhibitors in cancer treatment clinicians need to be aware of this rare yet treatable irAE. Given the morbidity and mortality associated with undiagnosed autoimmune diabetes we recommend routine HbA1c and plasma glucose testing in all patients prior to and during treatment with PD-1/PD-L1 inhibitors until more evidence has accumulated on identifying those patients with a pre-treatment risk of such irAEs.
引用
收藏
页码:235 / 241
页数:7
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