PD-1 inhibitor-associated type 1 diabetes: A case report and systematic review

ObjectiveThis study aimed to summarize the clinical characteristics of programmed death receptor 1 (PD-1) inhibitor-associated type 1 diabetes so as to improve the ability of clinicians to correctly diagnose and treat it.MethodsWe reported a case of a 70-year-old woman with gastric cancer who develo...

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Main Authors: Cuiping Lin (Author), Xuan Li (Author), Yu Qiu (Author), Zheng Chen (Author), Jianping Liu (Author)
Format: Book
Published: Frontiers Media S.A., 2022-08-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Cuiping Lin  |e author 
700 1 0 |a Xuan Li  |e author 
700 1 0 |a Yu Qiu  |e author 
700 1 0 |a Zheng Chen  |e author 
700 1 0 |a Jianping Liu  |e author 
245 0 0 |a PD-1 inhibitor-associated type 1 diabetes: A case report and systematic review 
260 |b Frontiers Media S.A.,   |c 2022-08-01T00:00:00Z. 
500 |a 2296-2565 
500 |a 10.3389/fpubh.2022.885001 
520 |a ObjectiveThis study aimed to summarize the clinical characteristics of programmed death receptor 1 (PD-1) inhibitor-associated type 1 diabetes so as to improve the ability of clinicians to correctly diagnose and treat it.MethodsWe reported a case of a 70-year-old woman with gastric cancer who developed hyperosmolar hyperglycemic coma during camrelizumab (a PD-1 inhibitor) treatment and was diagnosed with PD-1 inhibitor-associated type 1 diabetes. We conducted a systematic review of 74 case reports of type 1 diabetes associated with PD-1 inhibitor therapy published before June 2022.ResultsThe patient developed type 1 diabetes with hyperosmolar hyperglycemic coma after receiving camrelizumab chemotherapy for 6 months (9 cycles). We searched 69 English articles comprising 75 patients, all of whom had been treated with a PD-1 inhibitor (nivolumab or pembrolizumab) and progressed to diabetes after an average of 6.11 (1-28) cycles. Nivolumab combined with ipilimumab (a cytotoxic T lymphocyte-associated protein 4 inhibitor) had the shortest onset (4.47 cycles on average). A total of 76% (57/75) of patients developed diabetic ketoacidosis (DKA) at onset, and 50.67% (38/75) of patients had C-peptide <0.1 ng/mL. Most of the patients were tested for insulin autoantibodies, with a positive rate of 33.33% (23/69); of these, 86.96% (20/23) were tested for glutamate decarboxylase antibody and 46.67% (35/75) were tested for human leukocyte antigen (HLA). HLA-DR4 was the most common type.ConclusionsThe progression of type 1 diabetes induced by PD-1 inhibitors is relatively rapid. Islet failure often occurs when detected, seriously endangering patients' lives. Patients treated with PD-1 inhibitors should closely monitor their plasma glucose level during treatment to detect, diagnose, and treat diabetes on time. 
546 |a EN 
690 |a PD-1 inhibitors 
690 |a diabetes 
690 |a immune checkpoint inhibitor 
690 |a camrelizumab 
690 |a insulin 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Frontiers in Public Health, Vol 10 (2022) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fpubh.2022.885001/full 
787 0 |n https://doaj.org/toc/2296-2565 
856 4 1 |u https://doaj.org/article/a3f5cf9b15f245d5bb17bc6daa7a1f45  |z Connect to this object online.