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Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response

OBJECTIVE: The study objective was to assess the safety and efficacy of a preemptive direct-acting antiviral therapy in lung transplants from hepatitis C virus donors to uninfected recipients. METHODS: This study is a prospective, open-label, nonrandomized, pilot trial. Recipients of hepatitis C vir...

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Autores principales: Villavicencio, Mauricio A., Li, Selena S., Leifer, Ann Marie, Gustafson, Jenna L., Osho, Asishana, Wolfe, Stanley, Raz, Yuval, Griffith, Jason, Neuringer, Isabel, Bethea, Emily, Gift, Thais, Waldman, Georgina, Astor, Todd, Langer, Nathaniel B., Chung, Raymond T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328796/
https://www.ncbi.nlm.nih.gov/pubmed/37425441
http://dx.doi.org/10.1016/j.xjon.2023.02.014
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author Villavicencio, Mauricio A.
Li, Selena S.
Leifer, Ann Marie
Gustafson, Jenna L.
Osho, Asishana
Wolfe, Stanley
Raz, Yuval
Griffith, Jason
Neuringer, Isabel
Bethea, Emily
Gift, Thais
Waldman, Georgina
Astor, Todd
Langer, Nathaniel B.
Chung, Raymond T.
author_facet Villavicencio, Mauricio A.
Li, Selena S.
Leifer, Ann Marie
Gustafson, Jenna L.
Osho, Asishana
Wolfe, Stanley
Raz, Yuval
Griffith, Jason
Neuringer, Isabel
Bethea, Emily
Gift, Thais
Waldman, Georgina
Astor, Todd
Langer, Nathaniel B.
Chung, Raymond T.
author_sort Villavicencio, Mauricio A.
collection PubMed
description OBJECTIVE: The study objective was to assess the safety and efficacy of a preemptive direct-acting antiviral therapy in lung transplants from hepatitis C virus donors to uninfected recipients. METHODS: This study is a prospective, open-label, nonrandomized, pilot trial. Recipients of hepatitis C virus nucleic acid test positive donor lungs underwent preemptive direct-acting antiviral therapy with glecaprevir 300 mg/pibrentasvir 120 mg for 8 weeks from January 1, 2019, to December 31, 2020. Recipients of nucleic acid test positive lungs were compared with recipients of lungs from nucleic acid test negative donors. Primary end points were Kaplan–Meier survival and sustained virologic response. Secondary outcomes included primary graft dysfunction, rejection, and infection. RESULTS: Fifty-nine lung transplantations were included: 16 nucleic acid test positive and 43 nucleic acid test negative. Twelve nucleic acid test positive recipients (75%) developed hepatitis C virus viremia. Median time to clearance was 7 days. All nucleic acid test positive patients had undetectable hepatitis C virus RNA by week 3, and all alive patients (n = 15) remained negative during follow-up with 100% sustained virologic response at 12 months. One nucleic acid test positive patient died of primary graft dysfunction and multiorgan failure. Three of 43 nucleic acid test negative patients (7%) had hepatitis C virus antibody positive donors. None of them developed hepatitis C virus viremia. One-year survival was 94% for nucleic acid test positive recipients and 91% for nucleic acid test negative recipients. There was no difference in primary graft dysfunction, rejection, or infection. One-year survival for nucleic acid test positive recipients was similar to a historical cohort of the Scientific Registry of Transplant Recipients (89%). CONCLUSIONS: Recipients of hepatitis C virus nucleic acid test positive lungs have similar survival as recipients of nucleic acid test negative lungs. Preemptive direct-acting antiviral therapy results in rapid viral clearance and sustained virologic response at 12 months. Preemptive direct-acting antiviral may partially prevent hepatitis C virus transmission.
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spelling pubmed-103287962023-07-09 Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response Villavicencio, Mauricio A. Li, Selena S. Leifer, Ann Marie Gustafson, Jenna L. Osho, Asishana Wolfe, Stanley Raz, Yuval Griffith, Jason Neuringer, Isabel Bethea, Emily Gift, Thais Waldman, Georgina Astor, Todd Langer, Nathaniel B. Chung, Raymond T. JTCVS Open Thoracic: Lung Transplantation: Clinical Trial OBJECTIVE: The study objective was to assess the safety and efficacy of a preemptive direct-acting antiviral therapy in lung transplants from hepatitis C virus donors to uninfected recipients. METHODS: This study is a prospective, open-label, nonrandomized, pilot trial. Recipients of hepatitis C virus nucleic acid test positive donor lungs underwent preemptive direct-acting antiviral therapy with glecaprevir 300 mg/pibrentasvir 120 mg for 8 weeks from January 1, 2019, to December 31, 2020. Recipients of nucleic acid test positive lungs were compared with recipients of lungs from nucleic acid test negative donors. Primary end points were Kaplan–Meier survival and sustained virologic response. Secondary outcomes included primary graft dysfunction, rejection, and infection. RESULTS: Fifty-nine lung transplantations were included: 16 nucleic acid test positive and 43 nucleic acid test negative. Twelve nucleic acid test positive recipients (75%) developed hepatitis C virus viremia. Median time to clearance was 7 days. All nucleic acid test positive patients had undetectable hepatitis C virus RNA by week 3, and all alive patients (n = 15) remained negative during follow-up with 100% sustained virologic response at 12 months. One nucleic acid test positive patient died of primary graft dysfunction and multiorgan failure. Three of 43 nucleic acid test negative patients (7%) had hepatitis C virus antibody positive donors. None of them developed hepatitis C virus viremia. One-year survival was 94% for nucleic acid test positive recipients and 91% for nucleic acid test negative recipients. There was no difference in primary graft dysfunction, rejection, or infection. One-year survival for nucleic acid test positive recipients was similar to a historical cohort of the Scientific Registry of Transplant Recipients (89%). CONCLUSIONS: Recipients of hepatitis C virus nucleic acid test positive lungs have similar survival as recipients of nucleic acid test negative lungs. Preemptive direct-acting antiviral therapy results in rapid viral clearance and sustained virologic response at 12 months. Preemptive direct-acting antiviral may partially prevent hepatitis C virus transmission. Elsevier 2023-03-10 /pmc/articles/PMC10328796/ /pubmed/37425441 http://dx.doi.org/10.1016/j.xjon.2023.02.014 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Thoracic: Lung Transplantation: Clinical Trial
Villavicencio, Mauricio A.
Li, Selena S.
Leifer, Ann Marie
Gustafson, Jenna L.
Osho, Asishana
Wolfe, Stanley
Raz, Yuval
Griffith, Jason
Neuringer, Isabel
Bethea, Emily
Gift, Thais
Waldman, Georgina
Astor, Todd
Langer, Nathaniel B.
Chung, Raymond T.
Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title_full Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title_fullStr Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title_full_unstemmed Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title_short Preemptive antiviral therapy in lung transplantation from hepatitis C donors results in a rapid and sustained virologic response
title_sort preemptive antiviral therapy in lung transplantation from hepatitis c donors results in a rapid and sustained virologic response
topic Thoracic: Lung Transplantation: Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328796/
https://www.ncbi.nlm.nih.gov/pubmed/37425441
http://dx.doi.org/10.1016/j.xjon.2023.02.014
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