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DOI 10.1002/hep.30046

Медицинская библиотека · Hepatology (Baltimore, Md.) · 2018

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

Клиническое исследование III фазыСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: 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. (ClinicalTrials.gov NCT02692703.) (Hepatology 2018; 00:000-000).

Для цитирования: 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.. Hepatology (Baltimore, Md.). 2018. DOI: 10.1002/hep.30046.

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