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A Pragmatic, Randomized Controlled Trial of Oral Antivirals for the Treatment of Chronic Hepatitis C: The PRIORITIZE Study.
Sulkowski, Mark S; Moon, Juhi S; Sherman, Kenneth E; Morelli, Giuseppe; Darling, Jama M; Muir, Andrew J; Khalili, Mandana; Fishbein, Dawn A; Hinestrosa, Federico; Shiffman, Mitchell L; Di Bisceglie, Adrian; Rajender Reddy, K; Pearlman, Brian; Lok, Anna S; Fried, Michael W; Stewart, Paul W; Peter, Joy; Wadsworth, Summer; Kixmiller, Scott; Sloan, Anquenette; Vainorius, Monika; Horne, Patrick M; Michael, Larry; Dong, Meichen; Evon, Donna M; Segal, Jodi B; Nelson, David R.
Afiliação
  • Sulkowski MS; Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Moon JS; Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Sherman KE; Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
  • Morelli G; Department of Gastroenterology, Hepatology & Nutrition, University of Florida, Gainesville, FL.
  • Darling JM; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Muir AJ; Division of Gastroenterology, Duke University, Durham, NC.
  • Khalili M; Department of Medicine, University of California San Francisco, Zuckerberg San Francisco General, Hospital and Trauma Center, San Francisco, CA.
  • Fishbein DA; Infectious Disease, Medstar Health Research Institute, Washington, DC.
  • Hinestrosa F; Infectious Disease, Orlando Immunology Center, Orlando, FL.
  • Shiffman ML; Department of Gastroenterology, Liver Institute of Virginia, Richmond, VA.
  • Di Bisceglie A; Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO.
  • Rajender Reddy K; Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Pearlman B; Department of Internal Medicine, Wellstar Health System, Atlanta, GA.
  • Lok AS; Department of Internal Medicine, University of Michigan, Ann Arbor, MI.
  • Fried MW; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Stewart PW; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Peter J; Department of Gastroenterology, Hepatology & Nutrition, University of Florida, Gainesville, FL.
  • Wadsworth S; PRIORITIZE Patient Engagement Group consultant, Garner, NC.
  • Kixmiller S; PRIORITIZE Patient Engagement Group consultant, Greensboro, NC.
  • Sloan A; PRIORITIZE Patient Engagement Group consultant, Pittsboro, NC.
  • Vainorius M; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Horne PM; Department of Gastroenterology, Hepatology & Nutrition, University of Florida, Gainesville, FL.
  • Michael L; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Dong M; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Evon DM; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Segal JB; Division of Internal Medicne, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Nelson DR; Department of Gastroenterology, Hepatology & Nutrition, University of Florida, Gainesville, FL.
Hepatology ; 74(6): 2952-2964, 2021 12.
Article em En | MEDLINE | ID: mdl-34255381
BACKGROUND AND AIMS: Multiple direct-acting antiviral (DAA) regimens are available to treat HCV genotype 1 infection. However, comparative effectiveness from randomized controlled trials of DAA regimens is unavailable. APPROACH AND RESULTS: We conducted a pragmatic randomized controlled trial (NCT02786537) to compare the effectiveness of DAAs for HCV genotype 1a or 1b on viral response, safety, tolerability, and medication nonadherence. Adults with compensated liver disease, HCV genotype 1, not pregnant or breastfeeding, and with health insurance likely to cover ledipasvir/sofosbuvir (LDV/SOF) were recruited from 34 US viral hepatitis clinics. Participants were randomized (± ribavirin) to LDV/SOF, elbasvir/grazoprevir (EBR/GZR), and paritaprevir/ritonavir/ombitasvir+dasabuvir (PrOD; treatment arm stopped early). Primary outcomes included sustained viral response at 12 weeks (SVR12), clinician-recorded adverse events, patient-reported symptoms, and medication nonadherence. Between June 2016 and March 2018, 1,609 participants were randomized. Among 1,128 participants who received ≥1 dose of EBR/GZR or LDV/SOF (± ribavirin), SVR12 was 95.2% (95% CI, 92.8%-97.6%) and 97.4% (95% CI, 95.5%-99.2%), respectively, with a difference estimate of 2.2% (-0.5% to 4.7%), falling within the "equivalence" interval (-5% to 5%). While most (56%) participants experienced adverse events, few were serious (4.2%) or severe (1.8%). In the absence of ribavirin, discontinuations due to adverse events were rare. Patient-reported symptoms and medication nonadherence were similar. Study limitations were dropout due to insurance denial and loss to follow-up after treatment, limiting the ability to measure SVR12. CONCLUSIONS: This pragmatic trial demonstrated high SVR12 for participants treated with EBR/GZR and LDV/SOF with few adverse effects. Overall, the two regimens were equivalent in effectiveness. The results support current HCV guidelines that do not distinguish between ribavirin-free EBR/GZR and LDV/SOF.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Hepacivirus / Hepatite C Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged80 Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Hepacivirus / Hepatite C Crônica Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged80 Idioma: En Ano de publicação: 2021 Tipo de documento: Article