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Olaparib-Induced Immune-Mediated Liver Injury

Immune-mediated drug-induced liver injury can be triggered by multiple classes of medications including immunotherapies. Olaparib is a first-in-class oral inhibitor of poly (adenosine diphosphate-ribose) polymerase (an enzyme involved in DNA replication and repair) that is approved as maintenance tr...

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Autores principales: Alshelleh, Mohammad, Park, Jennifer, John, Veena, Rishi, Arvind, Bernstein, David, Roth, Nitzan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751767/
https://www.ncbi.nlm.nih.gov/pubmed/35028326
http://dx.doi.org/10.14309/crj.0000000000000735
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author Alshelleh, Mohammad
Park, Jennifer
John, Veena
Rishi, Arvind
Bernstein, David
Roth, Nitzan
author_facet Alshelleh, Mohammad
Park, Jennifer
John, Veena
Rishi, Arvind
Bernstein, David
Roth, Nitzan
author_sort Alshelleh, Mohammad
collection PubMed
description Immune-mediated drug-induced liver injury can be triggered by multiple classes of medications including immunotherapies. Olaparib is a first-in-class oral inhibitor of poly (adenosine diphosphate-ribose) polymerase (an enzyme involved in DNA replication and repair) that is approved as maintenance treatment in platinum-sensitive, epithelial ovarian, tubal, or primary peritoneal cancers with breast cancer 1/2 mutation. We report the first case in the United States of an acute and severe liver injury with associated jaundice and liver synthetic dysfunction secondary to olaparib. The liver injury was resolved with drug cessation and treatment with prednisone taper.
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spelling pubmed-87517672022-01-12 Olaparib-Induced Immune-Mediated Liver Injury Alshelleh, Mohammad Park, Jennifer John, Veena Rishi, Arvind Bernstein, David Roth, Nitzan ACG Case Rep J Case Report Immune-mediated drug-induced liver injury can be triggered by multiple classes of medications including immunotherapies. Olaparib is a first-in-class oral inhibitor of poly (adenosine diphosphate-ribose) polymerase (an enzyme involved in DNA replication and repair) that is approved as maintenance treatment in platinum-sensitive, epithelial ovarian, tubal, or primary peritoneal cancers with breast cancer 1/2 mutation. We report the first case in the United States of an acute and severe liver injury with associated jaundice and liver synthetic dysfunction secondary to olaparib. The liver injury was resolved with drug cessation and treatment with prednisone taper. Wolters Kluwer 2022-01-10 /pmc/articles/PMC8751767/ /pubmed/35028326 http://dx.doi.org/10.14309/crj.0000000000000735 Text en © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Alshelleh, Mohammad
Park, Jennifer
John, Veena
Rishi, Arvind
Bernstein, David
Roth, Nitzan
Olaparib-Induced Immune-Mediated Liver Injury
title Olaparib-Induced Immune-Mediated Liver Injury
title_full Olaparib-Induced Immune-Mediated Liver Injury
title_fullStr Olaparib-Induced Immune-Mediated Liver Injury
title_full_unstemmed Olaparib-Induced Immune-Mediated Liver Injury
title_short Olaparib-Induced Immune-Mediated Liver Injury
title_sort olaparib-induced immune-mediated liver injury
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751767/
https://www.ncbi.nlm.nih.gov/pubmed/35028326
http://dx.doi.org/10.14309/crj.0000000000000735
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