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Screening and prevention of hepatitis C virus reactivation during chemotherapy

Hepatitis C virus (HCV) reactivation occurs in 23% of HCV-infected cancer patients receiving chemotherapy. Forty-three percent of the patients with reactivation of HCV during chemotherapy develop a hepatitis flare. Most of the cancer patients with HCV reactivation have an unremarkable clinical cours...

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Autores principales: Li, Yuan-Rung, Hu, Tsung-Hui, Chen, Wen-Chi, Hsu, Ping-I, Chen, Hui-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384748/
https://www.ncbi.nlm.nih.gov/pubmed/34497443
http://dx.doi.org/10.3748/wjg.v27.i31.5181
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author Li, Yuan-Rung
Hu, Tsung-Hui
Chen, Wen-Chi
Hsu, Ping-I
Chen, Hui-Chun
author_facet Li, Yuan-Rung
Hu, Tsung-Hui
Chen, Wen-Chi
Hsu, Ping-I
Chen, Hui-Chun
author_sort Li, Yuan-Rung
collection PubMed
description Hepatitis C virus (HCV) reactivation occurs in 23% of HCV-infected cancer patients receiving chemotherapy. Forty-three percent of the patients with reactivation of HCV during chemotherapy develop a hepatitis flare. Most of the cancer patients with HCV reactivation have an unremarkable clinical course following an HCV-related hepatitis flare during chemotherapy. However, 26%–57% of the cancer patients developing an acute flare of chronic hepatitis C during chemotherapy require unanticipated discontinuation or dose reduction of chemotherapy, which results in deleterious changes in the cancer treatment plan. Although an optimal strategy for HCV screening in cancer patients receiving chemotherapy has not been established, universal pre-chemotherapy HCV testing for patients with hematological malignancies is recommended by current guidelines. All the currently approved direct-acting antivirals (DAAs) can be used in cancer patients, but the use of DAAs during chemotherapy should avoid drug–drug interactions between chemotherapy and antiviral agents. If there are no contraindications or anticipated drug–drug interactions, DAAs treatment can be administered before, during, or after chemotherapy. In conclusion, HCV reactivation occurs in approximately one-fourth of HCV-infected cancer patients receiving chemotherapy. An HCV-related hepatitis flare during chemotherapy may lead to the discontinuation of potentially life-saving chemotherapy. Currently, universal HCV screening is recommended in hematological malignancy patients before chemotherapy, but there is no evidence-based guideline for other cancer patients. DAAs treatment can cure HCV infection and prevent HCV reactivation during chemotherapy.
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spelling pubmed-83847482021-09-07 Screening and prevention of hepatitis C virus reactivation during chemotherapy Li, Yuan-Rung Hu, Tsung-Hui Chen, Wen-Chi Hsu, Ping-I Chen, Hui-Chun World J Gastroenterol Minireviews Hepatitis C virus (HCV) reactivation occurs in 23% of HCV-infected cancer patients receiving chemotherapy. Forty-three percent of the patients with reactivation of HCV during chemotherapy develop a hepatitis flare. Most of the cancer patients with HCV reactivation have an unremarkable clinical course following an HCV-related hepatitis flare during chemotherapy. However, 26%–57% of the cancer patients developing an acute flare of chronic hepatitis C during chemotherapy require unanticipated discontinuation or dose reduction of chemotherapy, which results in deleterious changes in the cancer treatment plan. Although an optimal strategy for HCV screening in cancer patients receiving chemotherapy has not been established, universal pre-chemotherapy HCV testing for patients with hematological malignancies is recommended by current guidelines. All the currently approved direct-acting antivirals (DAAs) can be used in cancer patients, but the use of DAAs during chemotherapy should avoid drug–drug interactions between chemotherapy and antiviral agents. If there are no contraindications or anticipated drug–drug interactions, DAAs treatment can be administered before, during, or after chemotherapy. In conclusion, HCV reactivation occurs in approximately one-fourth of HCV-infected cancer patients receiving chemotherapy. An HCV-related hepatitis flare during chemotherapy may lead to the discontinuation of potentially life-saving chemotherapy. Currently, universal HCV screening is recommended in hematological malignancy patients before chemotherapy, but there is no evidence-based guideline for other cancer patients. DAAs treatment can cure HCV infection and prevent HCV reactivation during chemotherapy. Baishideng Publishing Group Inc 2021-08-21 2021-08-21 /pmc/articles/PMC8384748/ /pubmed/34497443 http://dx.doi.org/10.3748/wjg.v27.i31.5181 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Minireviews
Li, Yuan-Rung
Hu, Tsung-Hui
Chen, Wen-Chi
Hsu, Ping-I
Chen, Hui-Chun
Screening and prevention of hepatitis C virus reactivation during chemotherapy
title Screening and prevention of hepatitis C virus reactivation during chemotherapy
title_full Screening and prevention of hepatitis C virus reactivation during chemotherapy
title_fullStr Screening and prevention of hepatitis C virus reactivation during chemotherapy
title_full_unstemmed Screening and prevention of hepatitis C virus reactivation during chemotherapy
title_short Screening and prevention of hepatitis C virus reactivation during chemotherapy
title_sort screening and prevention of hepatitis c virus reactivation during chemotherapy
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384748/
https://www.ncbi.nlm.nih.gov/pubmed/34497443
http://dx.doi.org/10.3748/wjg.v27.i31.5181
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