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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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). |
format | Online Article Text |
id | pubmed-6220874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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