BMJ Case Reports · 2017 · 26 citations · 5 references
MedicineImmunologyOncologyCancer ImmunologyImmunotherapyTumor ImmunologyAutoantibodiesDiabetes ManagementDiabetes MellitusDiabetic KetoacidosisGenitourinary Cancer PharmacotherapyImmune Checkpoint InhibitorsAtezolizumab TherapyDurvalumab TherapyMetastatic Squamous Cell CarcinomaPapillary Urothelial NeoplasmsPd-l1 BlockadeProgrammed Cell Death Ligand 1 InhibitionProgrammed Cell Death Ligand 1 SignalingProgrammed Death-ligand 1 Inhibitors
An 84-year-old woman with metastatic squamous cell carcinoma of the nasopharynx and no history of diabetes was started on the antiprogrammed cell death ligand-1 (anti-PD-L1) antibody durvalumab. Four months later, she presented in diabetic ketoacidosis with glucose 488 mg/dL, anion gap 16, positive serum ketones and A 1C 9.1%. Antiglutamic acid decarboxylase 65 (GAD) antibody was 13 U/mL (normal, <0.5 U/mL), c-peptide 0.4 ng/dL (normal, 1.1–4.3 ng/mL) and glucose 142 mg/dL. A man with metastatic papillary urothelial carcinoma was treated with the PD-L1 inhibitor atezolizumab. He had no history of diabetes. Nine weeks after initiation, he developed fatigue and polyuria with blood glucose 336 mg/dL, c-peptide 0.6 ng/mL, A 1C 8.2% and GAD antibodies 28.4 U/mL (normal, <1 U/mL). Due to the diagnosis of autoimmune diabetes, both patients were treated with insulin. Autoimmune diabetes is a rare immune-related adverse effect of PD-L1 inhibitors. We present the first two cases with documented positive pancreatic autoantibodies.
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Mechanisms of PDL1-mediated regulation of autoimmune diabetes
Indira Guleria, Melanie Gubbels Bupp, Shirine Dada et al. · Clinical Immunology · 2007 · 127 citations