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Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events

Background and aims: Current guidelines state that infliximab is contraindicated for the treatment of immune checkpoint inhibitor-related hepatitis (ir-hepatitis) due to the risk of inducing further liver damage. As this recommendation is largely based on the use of infliximab for rheumatologic dise...

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Autores principales: Araujo, Daniel V., Muniz, Thiago Pimentel, Yang, Anjie, Keshavarzi, Sareh, Sorotsky, Hadas, Butler, Marcus O., Saibil, Samuel, Spreafico, Anna, Hogg, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293058/
https://www.ncbi.nlm.nih.gov/pubmed/34208089
http://dx.doi.org/10.3390/curroncol28030201
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author Araujo, Daniel V.
Muniz, Thiago Pimentel
Yang, Anjie
Keshavarzi, Sareh
Sorotsky, Hadas
Butler, Marcus O.
Saibil, Samuel
Spreafico, Anna
Hogg, David
author_facet Araujo, Daniel V.
Muniz, Thiago Pimentel
Yang, Anjie
Keshavarzi, Sareh
Sorotsky, Hadas
Butler, Marcus O.
Saibil, Samuel
Spreafico, Anna
Hogg, David
author_sort Araujo, Daniel V.
collection PubMed
description Background and aims: Current guidelines state that infliximab is contraindicated for the treatment of immune checkpoint inhibitor-related hepatitis (ir-hepatitis) due to the risk of inducing further liver damage. As this recommendation is largely based on the use of infliximab for rheumatologic diseases, we evaluated the efficacy and hepatotoxicity of infliximab in patients with steroid-refractory immune-related adverse events (irAEs). Methods: We retrospectively reviewed consecutive patients treated with infliximab for irAEs at Princess Margaret Cancer Centre. To assess hepatotoxicity, we compared the mean value of ALT, AST, and total bilirubin (BT) before and after infliximab treatment. We used logistic regression to assess factors associated with infliximab efficacy. Results: Between January 2010 and February 2019, 56 patients were identified. The median age of the patients was 63 (27–84) years. Colitis was the most frequent toxicity (66%), followed by pneumonitis (11%). Infliximab was used to treat ir-hepatitis in one patient. The median number of infliximab doses was 1 (1–3) and led to toxicity resolution in 43 (76%) patients. The mean ALT, AST, and BT levels before and after infliximab treatment were not statistically different. The patient treated for ir-hepatitis had a complete recovery, with no incremental liver toxicity. Conclusions: In this dose-limited setting, infliximab was effective in resolving irAEs and did not induce hepatotoxicity.
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spelling pubmed-82930582021-07-22 Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events Araujo, Daniel V. Muniz, Thiago Pimentel Yang, Anjie Keshavarzi, Sareh Sorotsky, Hadas Butler, Marcus O. Saibil, Samuel Spreafico, Anna Hogg, David Curr Oncol Communication Background and aims: Current guidelines state that infliximab is contraindicated for the treatment of immune checkpoint inhibitor-related hepatitis (ir-hepatitis) due to the risk of inducing further liver damage. As this recommendation is largely based on the use of infliximab for rheumatologic diseases, we evaluated the efficacy and hepatotoxicity of infliximab in patients with steroid-refractory immune-related adverse events (irAEs). Methods: We retrospectively reviewed consecutive patients treated with infliximab for irAEs at Princess Margaret Cancer Centre. To assess hepatotoxicity, we compared the mean value of ALT, AST, and total bilirubin (BT) before and after infliximab treatment. We used logistic regression to assess factors associated with infliximab efficacy. Results: Between January 2010 and February 2019, 56 patients were identified. The median age of the patients was 63 (27–84) years. Colitis was the most frequent toxicity (66%), followed by pneumonitis (11%). Infliximab was used to treat ir-hepatitis in one patient. The median number of infliximab doses was 1 (1–3) and led to toxicity resolution in 43 (76%) patients. The mean ALT, AST, and BT levels before and after infliximab treatment were not statistically different. The patient treated for ir-hepatitis had a complete recovery, with no incremental liver toxicity. Conclusions: In this dose-limited setting, infliximab was effective in resolving irAEs and did not induce hepatotoxicity. MDPI 2021-06-11 /pmc/articles/PMC8293058/ /pubmed/34208089 http://dx.doi.org/10.3390/curroncol28030201 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Araujo, Daniel V.
Muniz, Thiago Pimentel
Yang, Anjie
Keshavarzi, Sareh
Sorotsky, Hadas
Butler, Marcus O.
Saibil, Samuel
Spreafico, Anna
Hogg, David
Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title_full Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title_fullStr Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title_full_unstemmed Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title_short Real World Outcomes and Hepatotoxicity of Infliximab in the Treatment of Steroid-Refractory Immune-Related Adverse Events
title_sort real world outcomes and hepatotoxicity of infliximab in the treatment of steroid-refractory immune-related adverse events
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293058/
https://www.ncbi.nlm.nih.gov/pubmed/34208089
http://dx.doi.org/10.3390/curroncol28030201
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