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Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma

BACKGROUND: There has been a significant improvement in survival of advanced malignancies with the advent of checkpoint inhibitors. These newer treatment modalities come with a wide spectrum of unique side effects, termed immune related adverse events (irAE), ranging from mild skin rash to severe co...

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Autores principales: Changizzadeh, Pouyan N., Mukkamalla, Shiva Kumar R., Armenio, Vincent A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735540/
https://www.ncbi.nlm.nih.gov/pubmed/29254501
http://dx.doi.org/10.1186/s40425-017-0303-9
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author Changizzadeh, Pouyan N.
Mukkamalla, Shiva Kumar R.
Armenio, Vincent A.
author_facet Changizzadeh, Pouyan N.
Mukkamalla, Shiva Kumar R.
Armenio, Vincent A.
author_sort Changizzadeh, Pouyan N.
collection PubMed
description BACKGROUND: There has been a significant improvement in survival of advanced malignancies with the advent of checkpoint inhibitors. These newer treatment modalities come with a wide spectrum of unique side effects, termed immune related adverse events (irAE), ranging from mild skin rash to severe colitis. Included in that spectrum is the rare side effect of autoimmune diabetes mellitus. Despite a few case reports illustrating the incidence of autoimmune diabetes associated with immunotherapy, there has not been much mentioned about exacerbation or acceleration of hyperglycemia in non-autoimmune settings leading to de novo diagnosis of type 2 diabetes mellitus. CASE PRESENTATION: We report the case of a 42 year old man with metastatic melanoma and no prior history of diabetes mellitus, who presented with diabetic ketoacidosis (DKA) after 3 cycles of combination checkpoint inhibitor therapy using nivolumab and ipilimumab. New onset diabetes mellitus was diagnosed on the basis of elevated hemoglobin A1c, in the absence of prior personal or family history. Autoimmune or type 1 diabetes mellitus was ruled out with normal levels of anti-glutamic acid decarboxylase 65 (GAD65) antibody, zinc transporter 8 (ZnT8) antibody, and islet antigen-2 (IA-2) antibody. CONCLUSIONS: This case report highlights the importance of recognizing rare but serious adverse events related to immunotherapy and incorporation of appropriate tools for early identification and management in national cancer treatment guidelines.
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spelling pubmed-57355402017-12-21 Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma Changizzadeh, Pouyan N. Mukkamalla, Shiva Kumar R. Armenio, Vincent A. J Immunother Cancer Case Report BACKGROUND: There has been a significant improvement in survival of advanced malignancies with the advent of checkpoint inhibitors. These newer treatment modalities come with a wide spectrum of unique side effects, termed immune related adverse events (irAE), ranging from mild skin rash to severe colitis. Included in that spectrum is the rare side effect of autoimmune diabetes mellitus. Despite a few case reports illustrating the incidence of autoimmune diabetes associated with immunotherapy, there has not been much mentioned about exacerbation or acceleration of hyperglycemia in non-autoimmune settings leading to de novo diagnosis of type 2 diabetes mellitus. CASE PRESENTATION: We report the case of a 42 year old man with metastatic melanoma and no prior history of diabetes mellitus, who presented with diabetic ketoacidosis (DKA) after 3 cycles of combination checkpoint inhibitor therapy using nivolumab and ipilimumab. New onset diabetes mellitus was diagnosed on the basis of elevated hemoglobin A1c, in the absence of prior personal or family history. Autoimmune or type 1 diabetes mellitus was ruled out with normal levels of anti-glutamic acid decarboxylase 65 (GAD65) antibody, zinc transporter 8 (ZnT8) antibody, and islet antigen-2 (IA-2) antibody. CONCLUSIONS: This case report highlights the importance of recognizing rare but serious adverse events related to immunotherapy and incorporation of appropriate tools for early identification and management in national cancer treatment guidelines. BioMed Central 2017-12-19 /pmc/articles/PMC5735540/ /pubmed/29254501 http://dx.doi.org/10.1186/s40425-017-0303-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Changizzadeh, Pouyan N.
Mukkamalla, Shiva Kumar R.
Armenio, Vincent A.
Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title_full Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title_fullStr Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title_full_unstemmed Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title_short Combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
title_sort combined checkpoint inhibitor therapy causing diabetic ketoacidosis in metastatic melanoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735540/
https://www.ncbi.nlm.nih.gov/pubmed/29254501
http://dx.doi.org/10.1186/s40425-017-0303-9
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