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Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin

Hodgkin’s lymphoma is commonly treated with a combination of chemotherapy drugs including doxorubicin, bleomycin, vinblastine, and dacarbazine. Antibody-drug conjugates such as brentuximab vedotin are now being used to treat Hodgkin’s lymphoma that has not responded to standard treatment. Brentuxima...

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Detalles Bibliográficos
Autores principales: Thakkar, Keval, Khurana, Sonali, Sun, Yujiao, Hembree, Timothy N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074015/
https://www.ncbi.nlm.nih.gov/pubmed/37025732
http://dx.doi.org/10.7759/cureus.35804
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author Thakkar, Keval
Khurana, Sonali
Sun, Yujiao
Hembree, Timothy N
author_facet Thakkar, Keval
Khurana, Sonali
Sun, Yujiao
Hembree, Timothy N
author_sort Thakkar, Keval
collection PubMed
description Hodgkin’s lymphoma is commonly treated with a combination of chemotherapy drugs including doxorubicin, bleomycin, vinblastine, and dacarbazine. Antibody-drug conjugates such as brentuximab vedotin are now being used to treat Hodgkin’s lymphoma that has not responded to standard treatment. Brentuximab vedotin is a monoclonal antibody that selectively delivers a cytotoxic agent, monomethyl auristatin E, which targets cells expressing surface CD30 markers, a protein that may be found in high amounts in some cancer cells including lymphoma cells. Common adverse effects of the drug include diarrhea, nausea, anemia, and fatigue. We present a case of a patient with diabetic ketoacidosis and profound insulin resistance secondary to brentuximab. Diabetic ketoacidosis is a rare but serious adverse reaction in this growing class of antibody-drug conjugates.
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spelling pubmed-100740152023-04-05 Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin Thakkar, Keval Khurana, Sonali Sun, Yujiao Hembree, Timothy N Cureus Internal Medicine Hodgkin’s lymphoma is commonly treated with a combination of chemotherapy drugs including doxorubicin, bleomycin, vinblastine, and dacarbazine. Antibody-drug conjugates such as brentuximab vedotin are now being used to treat Hodgkin’s lymphoma that has not responded to standard treatment. Brentuximab vedotin is a monoclonal antibody that selectively delivers a cytotoxic agent, monomethyl auristatin E, which targets cells expressing surface CD30 markers, a protein that may be found in high amounts in some cancer cells including lymphoma cells. Common adverse effects of the drug include diarrhea, nausea, anemia, and fatigue. We present a case of a patient with diabetic ketoacidosis and profound insulin resistance secondary to brentuximab. Diabetic ketoacidosis is a rare but serious adverse reaction in this growing class of antibody-drug conjugates. Cureus 2023-03-05 /pmc/articles/PMC10074015/ /pubmed/37025732 http://dx.doi.org/10.7759/cureus.35804 Text en Copyright © 2023, Thakkar et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Thakkar, Keval
Khurana, Sonali
Sun, Yujiao
Hembree, Timothy N
Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title_full Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title_fullStr Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title_full_unstemmed Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title_short Diabetic Ketoacidosis and Profound Insulin Resistance From Brentuximab Vedotin
title_sort diabetic ketoacidosis and profound insulin resistance from brentuximab vedotin
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074015/
https://www.ncbi.nlm.nih.gov/pubmed/37025732
http://dx.doi.org/10.7759/cureus.35804
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