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Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection

Well‐tolerated, ribavirin‐free, pangenotypic hepatitis C virus (HCV) treatments for transplant recipients remain a high priority. Once‐daily glecaprevir/pibrentasvir demonstrates high rates of sustained virologic response at 12 weeks posttreatment (SVR12) across all major HCV genotypes (GTs). This t...

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Autores principales: Reau, Nancy, Kwo, Paul Y., Rhee, Susan, Brown, Robert S., Agarwal, Kosh, Angus, Peter, Gane, Edward, Kao, Jia‐Horng, Mantry, Parvez S., Mutimer, David, Reddy, K. Rajender, Tran, Tram T., Hu, Yiran B., Gulati, Abhishek, Krishnan, Preethi, Dumas, Emily O., Porcalla, Ariel, Shulman, Nancy S., Liu, Wei, Samanta, Suvajit, Trinh, Roger, Forns, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220874/
https://www.ncbi.nlm.nih.gov/pubmed/29672891
http://dx.doi.org/10.1002/hep.30046
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author Reau, Nancy
Kwo, Paul Y.
Rhee, Susan
Brown, Robert S.
Agarwal, Kosh
Angus, Peter
Gane, Edward
Kao, Jia‐Horng
Mantry, Parvez S.
Mutimer, David
Reddy, K. Rajender
Tran, Tram T.
Hu, Yiran B.
Gulati, Abhishek
Krishnan, Preethi
Dumas, Emily O.
Porcalla, Ariel
Shulman, Nancy S.
Liu, Wei
Samanta, Suvajit
Trinh, Roger
Forns, Xavier
author_facet Reau, Nancy
Kwo, Paul Y.
Rhee, Susan
Brown, Robert S.
Agarwal, Kosh
Angus, Peter
Gane, Edward
Kao, Jia‐Horng
Mantry, Parvez S.
Mutimer, David
Reddy, K. Rajender
Tran, Tram T.
Hu, Yiran B.
Gulati, Abhishek
Krishnan, Preethi
Dumas, Emily O.
Porcalla, Ariel
Shulman, Nancy S.
Liu, Wei
Samanta, Suvajit
Trinh, Roger
Forns, Xavier
author_sort Reau, Nancy
collection PubMed
description Well‐tolerated, ribavirin‐free, pangenotypic hepatitis C virus (HCV) treatments for transplant recipients remain a high priority. Once‐daily glecaprevir/pibrentasvir demonstrates high rates of sustained virologic response at 12 weeks posttreatment (SVR12) across all major HCV genotypes (GTs). This trial evaluated the safety and efficacy of glecaprevir/pibrentasvir for patients with chronic HCV GT1‐6 infection who had received a liver or kidney transplant. MAGELLAN‐2 was a phase 3, open‐label trial conducted in patients who were ≥3 months posttransplant. Patients without cirrhosis who were HCV treatment‐naive (GT1‐6) or treatment‐experienced (GT1, 2, 4‐6; with interferon‐based therapy with or without sofosbuvir, or sofosbuvir plus ribavirin) received glecaprevir/pibrentasvir (300/120 mg) once daily for 12 weeks. The primary endpoint compared the percentage of patients receiving glecaprevir/pibrentasvir with SVR12 to a historic SVR12 rate based on the standard of care. Safety of glecaprevir/pibrentasvir was assessed. In total, 80 liver transplant and 20 kidney transplant patients participated in the trial. Most patients had no or minimal fibrosis (80% had fibrosis scores F0‐F1) and were infected with HCV GT1 (57%) or GT3 (24%). The overall SVR12 was 98% (n/N = 98/100; 95% confidence interval, 95.3%–100%), which exceeded the prespecified historic standard‐of‐care SVR12 threshold of 94%. One patient experienced virologic failure. One patient discontinued because of an adverse event considered to be unrelated to treatment; this patient achieved SVR12. Adverse events were mostly mild in severity, and laboratory abnormalities were infrequent. Conclusion: Once‐daily glecaprevir/pibrentasvir for 12 weeks is a well‐tolerated and efficacious, ribavirin‐free treatment for patients with chronic HCV GT1‐6 infection who have received a liver or kidney transplant. (http://ClinicalTrials.gov NCT02692703.) (Hepatology 2018; 00:000‐000).
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spelling pubmed-62208742018-11-13 Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection Reau, Nancy Kwo, Paul Y. Rhee, Susan Brown, Robert S. Agarwal, Kosh Angus, Peter Gane, Edward Kao, Jia‐Horng Mantry, Parvez S. Mutimer, David Reddy, K. Rajender Tran, Tram T. Hu, Yiran B. Gulati, Abhishek Krishnan, Preethi Dumas, Emily O. Porcalla, Ariel Shulman, Nancy S. Liu, Wei Samanta, Suvajit Trinh, Roger Forns, Xavier Hepatology Original Articles Well‐tolerated, ribavirin‐free, pangenotypic hepatitis C virus (HCV) treatments for transplant recipients remain a high priority. Once‐daily glecaprevir/pibrentasvir demonstrates high rates of sustained virologic response at 12 weeks posttreatment (SVR12) across all major HCV genotypes (GTs). This trial evaluated the safety and efficacy of glecaprevir/pibrentasvir for patients with chronic HCV GT1‐6 infection who had received a liver or kidney transplant. MAGELLAN‐2 was a phase 3, open‐label trial conducted in patients who were ≥3 months posttransplant. Patients without cirrhosis who were HCV treatment‐naive (GT1‐6) or treatment‐experienced (GT1, 2, 4‐6; with interferon‐based therapy with or without sofosbuvir, or sofosbuvir plus ribavirin) received glecaprevir/pibrentasvir (300/120 mg) once daily for 12 weeks. The primary endpoint compared the percentage of patients receiving glecaprevir/pibrentasvir with SVR12 to a historic SVR12 rate based on the standard of care. Safety of glecaprevir/pibrentasvir was assessed. In total, 80 liver transplant and 20 kidney transplant patients participated in the trial. Most patients had no or minimal fibrosis (80% had fibrosis scores F0‐F1) and were infected with HCV GT1 (57%) or GT3 (24%). The overall SVR12 was 98% (n/N = 98/100; 95% confidence interval, 95.3%–100%), which exceeded the prespecified historic standard‐of‐care SVR12 threshold of 94%. One patient experienced virologic failure. One patient discontinued because of an adverse event considered to be unrelated to treatment; this patient achieved SVR12. Adverse events were mostly mild in severity, and laboratory abnormalities were infrequent. Conclusion: Once‐daily glecaprevir/pibrentasvir for 12 weeks is a well‐tolerated and efficacious, ribavirin‐free treatment for patients with chronic HCV GT1‐6 infection who have received a liver or kidney transplant. (http://ClinicalTrials.gov NCT02692703.) (Hepatology 2018; 00:000‐000). John Wiley and Sons Inc. 2018-07-25 2018-10 /pmc/articles/PMC6220874/ /pubmed/29672891 http://dx.doi.org/10.1002/hep.30046 Text en © 2018 The Authors. Hepatology published by Wiley Periodicals, Inc. on behalf of American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Reau, Nancy
Kwo, Paul Y.
Rhee, Susan
Brown, Robert S.
Agarwal, Kosh
Angus, Peter
Gane, Edward
Kao, Jia‐Horng
Mantry, Parvez S.
Mutimer, David
Reddy, K. Rajender
Tran, Tram T.
Hu, Yiran B.
Gulati, Abhishek
Krishnan, Preethi
Dumas, Emily O.
Porcalla, Ariel
Shulman, Nancy S.
Liu, Wei
Samanta, Suvajit
Trinh, Roger
Forns, Xavier
Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title_full Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title_fullStr Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title_full_unstemmed Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title_short Glecaprevir/Pibrentasvir Treatment in Liver or Kidney Transplant Patients With Hepatitis C Virus Infection
title_sort glecaprevir/pibrentasvir treatment in liver or kidney transplant patients with hepatitis c virus infection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220874/
https://www.ncbi.nlm.nih.gov/pubmed/29672891
http://dx.doi.org/10.1002/hep.30046
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