Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer

Context: Immune checkpoint inhibitors (ICIs), now FDA-approved, are increasingly used as an effective treatment of various cancers. Autoimmune diabetes is a rare but life-threatening endocrine adverse event, which has been reported in patients treated with anti-programmed-cell death-1 (anti-PD-1) an...

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Main Authors: Jin Sothornwit, Anakapong Phunmanee, Chatlert Pongchaiyakul
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2019.00352/full
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author Jin Sothornwit
Anakapong Phunmanee
Chatlert Pongchaiyakul
author_facet Jin Sothornwit
Anakapong Phunmanee
Chatlert Pongchaiyakul
author_sort Jin Sothornwit
collection DOAJ
description Context: Immune checkpoint inhibitors (ICIs), now FDA-approved, are increasingly used as an effective treatment of various cancers. Autoimmune diabetes is a rare but life-threatening endocrine adverse event, which has been reported in patients treated with anti-programmed-cell death-1 (anti-PD-1) and anti-programmed-cell death-1 ligand (anti-PD-L1) therapies.Case description: We report a 52-year-old woman with advanced-stage non-small cell lung cancer who presented with diabetic ketoacidosis (DKA) at 24 weeks after atezolizumab initiation. She initially received oral antidiabetic medication from primary care hospital and experienced recurrent DKA 3 days later. Her plasma glucose on the day that she had recurrent DKA was 332 mg/dL (18.4 mmol/L), A1c was 7.9% (63 mmol/mol), fasting C-peptide was <0.03 nmol/L (0.1 ng/ml), fasting insulin level was <1 μIU/ml, anti-glutamic acid decarboxylase 65 (GADA) was 7.2 U/ml (normal, >5 U/ml), and human leukocyte antigen (HLA) class II typing was DR3-DQ2/DR14-DQ5. A diagnosis of autoimmune diabetes was made. After treatment for DKA, she recovered and received basal-bolus insulin treatment. Atezolizumab had been discontinued after the fifth cycle, prior to the development of DKA, due to progression of lung cancer.Conclusion: To date, there has been neither an effective way to detect if a patient is at high risk for autoimmune diabetes nor to prevent the complications associated with it. Regular glucose monitoring is the best method of early diabetes detection. In patients with new onset diabetes following treatment with ICIs, C-peptide levels and GADA should be screened, and insulin therapy should be prescribed to prevent hyperglycemic emergency while waiting for definite diagnosis.
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spelling doaj.art-9615dae89aab42a682f4abdd269a85742022-12-22T01:40:59ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922019-06-011010.3389/fendo.2019.00352461260Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung CancerJin Sothornwit0Anakapong Phunmanee1Chatlert Pongchaiyakul2Division of Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, ThailandDivision of Critical Care, Department of Internal Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, ThailandDivision of Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, ThailandContext: Immune checkpoint inhibitors (ICIs), now FDA-approved, are increasingly used as an effective treatment of various cancers. Autoimmune diabetes is a rare but life-threatening endocrine adverse event, which has been reported in patients treated with anti-programmed-cell death-1 (anti-PD-1) and anti-programmed-cell death-1 ligand (anti-PD-L1) therapies.Case description: We report a 52-year-old woman with advanced-stage non-small cell lung cancer who presented with diabetic ketoacidosis (DKA) at 24 weeks after atezolizumab initiation. She initially received oral antidiabetic medication from primary care hospital and experienced recurrent DKA 3 days later. Her plasma glucose on the day that she had recurrent DKA was 332 mg/dL (18.4 mmol/L), A1c was 7.9% (63 mmol/mol), fasting C-peptide was <0.03 nmol/L (0.1 ng/ml), fasting insulin level was <1 μIU/ml, anti-glutamic acid decarboxylase 65 (GADA) was 7.2 U/ml (normal, >5 U/ml), and human leukocyte antigen (HLA) class II typing was DR3-DQ2/DR14-DQ5. A diagnosis of autoimmune diabetes was made. After treatment for DKA, she recovered and received basal-bolus insulin treatment. Atezolizumab had been discontinued after the fifth cycle, prior to the development of DKA, due to progression of lung cancer.Conclusion: To date, there has been neither an effective way to detect if a patient is at high risk for autoimmune diabetes nor to prevent the complications associated with it. Regular glucose monitoring is the best method of early diabetes detection. In patients with new onset diabetes following treatment with ICIs, C-peptide levels and GADA should be screened, and insulin therapy should be prescribed to prevent hyperglycemic emergency while waiting for definite diagnosis.https://www.frontiersin.org/article/10.3389/fendo.2019.00352/fullatezolizumabautoimmunitycheckpoint inhibitordiabetes mellitusimmunotherapy
spellingShingle Jin Sothornwit
Anakapong Phunmanee
Chatlert Pongchaiyakul
Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
Frontiers in Endocrinology
atezolizumab
autoimmunity
checkpoint inhibitor
diabetes mellitus
immunotherapy
title Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
title_full Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
title_fullStr Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
title_full_unstemmed Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
title_short Atezolizumab-Induced Autoimmune Diabetes in a Patient With Metastatic Lung Cancer
title_sort atezolizumab induced autoimmune diabetes in a patient with metastatic lung cancer
topic atezolizumab
autoimmunity
checkpoint inhibitor
diabetes mellitus
immunotherapy
url https://www.frontiersin.org/article/10.3389/fendo.2019.00352/full
work_keys_str_mv AT jinsothornwit atezolizumabinducedautoimmunediabetesinapatientwithmetastaticlungcancer
AT anakapongphunmanee atezolizumabinducedautoimmunediabetesinapatientwithmetastaticlungcancer
AT chatlertpongchaiyakul atezolizumabinducedautoimmunediabetesinapatientwithmetastaticlungcancer