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Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review
Nowadays, immune checkpoint inhibitor therapy has been used in more and more cancer patients. These agents were associated with immune-related adverse effects, and autoimmune diabetes mellitus is one of them. And it is not common but can be potentially fatal. Anti PD-1 monoclonal antibody is a human...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225154/ https://www.ncbi.nlm.nih.gov/pubmed/32420079 http://dx.doi.org/10.21037/tlcr.2020.03.05 |
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author | Li, Wei Wang, Hao Chen, Bin Zhao, Sha Zhang, Xiaoshen Jia, Keyi Deng, Juan He, Yayi Zhou, Caicun |
author_facet | Li, Wei Wang, Hao Chen, Bin Zhao, Sha Zhang, Xiaoshen Jia, Keyi Deng, Juan He, Yayi Zhou, Caicun |
author_sort | Li, Wei |
collection | PubMed |
description | Nowadays, immune checkpoint inhibitor therapy has been used in more and more cancer patients. These agents were associated with immune-related adverse effects, and autoimmune diabetes mellitus is one of them. And it is not common but can be potentially fatal. Anti PD-1 monoclonal antibody is a humanized IgG4 antibody against PD-1, which has been applied in advanced non-small cell lung cancer (NSCLC) treatment. In this paper, we reported the case of autoimmune diabetes mellitus induced by anti PD-1 monoclonal antibody in NSCLC treatment. Here is a 73-year-old male patient with no diabetes history who had anti PD-1 monoclonal antibody 200 mg every 3 weeks for NSCLC treatment. After 10 cycles of the therapy, his blood glucose level elevated and he suffered diabetic ketoacidosis (DKA). And his C-peptide was significantly decreased with negative relative auto-antibodies. Combined with his medical history and the laboratory examination, anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus was diagnosed. After recovering from DKA and controlling his blood glucose, his anti PD-1 therapy was continued and he still got some benefit. This report suggested that glycemic monitoring is imperative during this anti PD-1 monoclonal antibody treatment. Moreover, after controlling the blood glucose level, continuing the immune therapy could still be benefit and safe for the patient. |
format | Online Article Text |
id | pubmed-7225154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-72251542020-05-15 Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review Li, Wei Wang, Hao Chen, Bin Zhao, Sha Zhang, Xiaoshen Jia, Keyi Deng, Juan He, Yayi Zhou, Caicun Transl Lung Cancer Res Case Report Nowadays, immune checkpoint inhibitor therapy has been used in more and more cancer patients. These agents were associated with immune-related adverse effects, and autoimmune diabetes mellitus is one of them. And it is not common but can be potentially fatal. Anti PD-1 monoclonal antibody is a humanized IgG4 antibody against PD-1, which has been applied in advanced non-small cell lung cancer (NSCLC) treatment. In this paper, we reported the case of autoimmune diabetes mellitus induced by anti PD-1 monoclonal antibody in NSCLC treatment. Here is a 73-year-old male patient with no diabetes history who had anti PD-1 monoclonal antibody 200 mg every 3 weeks for NSCLC treatment. After 10 cycles of the therapy, his blood glucose level elevated and he suffered diabetic ketoacidosis (DKA). And his C-peptide was significantly decreased with negative relative auto-antibodies. Combined with his medical history and the laboratory examination, anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus was diagnosed. After recovering from DKA and controlling his blood glucose, his anti PD-1 therapy was continued and he still got some benefit. This report suggested that glycemic monitoring is imperative during this anti PD-1 monoclonal antibody treatment. Moreover, after controlling the blood glucose level, continuing the immune therapy could still be benefit and safe for the patient. AME Publishing Company 2020-04 /pmc/articles/PMC7225154/ /pubmed/32420079 http://dx.doi.org/10.21037/tlcr.2020.03.05 Text en 2020 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Li, Wei Wang, Hao Chen, Bin Zhao, Sha Zhang, Xiaoshen Jia, Keyi Deng, Juan He, Yayi Zhou, Caicun Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title | Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title_full | Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title_fullStr | Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title_full_unstemmed | Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title_short | Anti PD-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
title_sort | anti pd-1 monoclonal antibody induced autoimmune diabetes mellitus: a case report and brief review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225154/ https://www.ncbi.nlm.nih.gov/pubmed/32420079 http://dx.doi.org/10.21037/tlcr.2020.03.05 |
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