Literature DB >> 28189751

Effectiveness, safety and clinical outcomes of direct-acting antiviral therapy in HCV genotype 1 infection: Results from a Spanish real-world cohort.

Jose Luis Calleja1, Javier Crespo2, Diego Rincón3, Belén Ruiz-Antorán4, Inmaculada Fernandez5, Christie Perelló4, Francisco Gea6, Sabela Lens7, Javier García-Samaniego8, Begoña Sacristán9, María García-Eliz10, Susana Llerena11, Juan Manuel Pascasio12, Juan Turnes13, Xavier Torras14, Rosa Maria Morillas15, Jordi Llaneras16, Miguel A Serra17, Moises Diago18, Conrado Fernández Rodriguez19, Javier Ampuero20, Francisco Jorquera21, Miguel A Simon22, Juan Arenas23, Carmen Alvarez Navascues24, Rafael Bañares3, Raquel Muñoz5, Agustin Albillos6, Zoe Mariño7.   

Abstract

BACKGROUND & AIMS: Clinical trials evaluating second-generation direct-acting antiviral agents (DAAs) have shown excellent rates of sustained virologic response (SVR) and good safety profiles in patients with chronic hepatitis C virus (HCV) genotype 1 infection. We aimed to investigate the effectiveness and safety of two oral DAA combination regimens, ombitasvir/paritaprevir/ritonavir plus dasabuvir (OMV/PTV/r+DSV) and ledipasvir/sofosbuvir (LDV/SOF), in a real-world clinical practice.
METHODS: Data from HCV genotype 1 patients treated with either OMV/PTV/r+DSV±ribavirin (RBV) (n=1567) or LDV/SOF±RBV (n=1758) in 35 centers across Spain between April 1, 2015 and February 28, 2016 were recorded in a large national database. Demographic, clinical and virological data were analyzed. Details of serious adverse events (SAEs) were recorded.
RESULTS: The two cohorts were not matched with respect to baseline characteristics and could not be compared directly. The SVR12 rate was 96.8% with OMV/PTVr/DSV±RBV and 95.8% with LDV/SOF±RBV. No significant differences were observed in SVR according to HCV subgenotype (p=0.321 [OMV/PTV/r+DSV±RBV] and p=0.174 [LDV/SOF]) or degree of fibrosis (c0.548 [OMV/PTV/r/DSV±RBV] and p=0.085 [LDV/SOF]). Only baseline albumin level was significantly associated with failure to achieve SVR (p<0.05) on multivariate analysis. Rates of SAEs and SAE-associated treatment discontinuation were 5.4% and 1.7%, in the OMV/PTV/r+DSV subcohort and 5.5% and 1.5% in the LDV/SOF subcohort, respectively. Hepatocellular carcinoma (HCC) recurred in 30% of patients with a complete response to therapy for previous HCC. Incident HCC was reported in 0.93%.
CONCLUSIONS: In this large cohort of patients managed in the real-world setting in Spain, OMV/PTV/r+DSV and LDV/SOF achieved high rates of SVR12, comparable to those observed in randomized controlled trials, with similarly good safety profiles. LAY
SUMMARY: In clinical trials, second-generation direct-acting antiviral agents (DAAs) have been shown to cure over 90% of patients chronically infected with the genotype 1 hepatitis C virus and have been better tolerated than previous treatment regimens. However, patients enrolled in clinical trials do not reflect the real patient population encountered in routine practice. The current study, which includes almost 4,000 patients, demonstrates comparable rates of cure with two increasingly used DAA combinations as those observed in the clinical trial environment, confirming that clinical trial findings with DAAs translate into the real-world setting, where patient populations are more diverse and complex.
Copyright © 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antiviral agents; Dasabuvir; Genotype 1; Hepatitis C, Chronic; Ledipasvir; Ombitasvir; Paritaprevir; Randomized controlled trials; Real-world; Ritonavir; Sofosbuvir; Sustained virologic response

Mesh:

Substances:

Year:  2017        PMID: 28189751     DOI: 10.1016/j.jhep.2017.01.028

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  55 in total

1.  Safety and Effectiveness of Ledipasvir and Sofosbuvir, With or Without Ribavirin, in Treatment-Experienced Patients With Genotype 1 Hepatitis C Virus Infection and Cirrhosis.

Authors:  Joseph K Lim; Ann Marie Liapakis; Mitchell L Shiffman; Anna S Lok; Stefan Zeuzem; Norah A Terrault; James S Park; Charles S Landis; Mohamed Hassan; Joel Gallant; Alexander Kuo; Paul J Pockros; Monika Vainorius; Lucy Akushevich; Larry Michael; Michael W Fried; David R Nelson; Ziv Ben-Ari
Journal:  Clin Gastroenterol Hepatol       Date:  2018-01-03       Impact factor: 11.382

Review 2.  Adjuvant treatment strategy after curative resection for hepatocellular carcinoma.

Authors:  Wei Zhang; Bixiang Zhang; Xiao-Ping Chen
Journal:  Front Med       Date:  2021-03-23       Impact factor: 4.592

3.  Risk of hepatocellular carcinoma for patients treated with direct-acting antivirals: steps after hepatitis C virus eradication to achieve elimination.

Authors:  Mei-Hsuan Lee
Journal:  Transl Gastroenterol Hepatol       Date:  2018-03-05

4.  Adjuvant ribavirin and longer direct-acting antiviral treatment duration improve sustained virological response among hepatitis C patients at risk of treatment failure.

Authors:  Mei Lu; Kuan-Han Wu; Jia Li; Anne C Moorman; Philip R Spradling; Eyasu H Teshale; Joseph A Boscarino; Yihe G Daida; Mark A Schmidt; Loralee B Rupp; Talan Zhang; Sheri Trudeau; Stuart C Gordon
Journal:  J Viral Hepat       Date:  2019-07-04       Impact factor: 3.728

5.  Impact of DAA-Based Regimens on HCV-Related Extra-Hepatic Damage: A Narrative Review.

Authors:  Evangelista Sagnelli; Caterina Sagnelli; Antonio Russo; Mariantonietta Pisaturo; Clarissa Camaioni; Roberta Astorri; Nicola Coppola
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

6.  Risk of De Novo Hepatocellular Carcinoma Following Use of Direct Acting Antiviral Medications for Treatment of Chronic Hepatitis C.

Authors:  Samuel O Antwi; Holly K Van Houten; Lindsey R Sangaralingham; Tushar Patel
Journal:  Cancer Prev Res (Phila)       Date:  2019-08-26

7.  Evolution of Hepatitis C Virus Treatment During the Era of Sofosbuvir-Based Therapies: A Real-World Experience in France.

Authors:  Denis Ouzan; Dominique Larrey; Dominique Guyader; André-Jean Remy; Ghassan Riachi; Fréderic Heluwaert; Régine Truchi; Jean-Marc Combis; François Bailly; Isabelle Rosa; Christophe Hézode; Denise Glorian-Petraud; Olivier Libert; Heribert Ramroth; Tarik Asselah; Gérard Thiefin; Dominique Roulot; Bruno Roche; Vincent Leroy; Jérôme Dumortier; Dominique Thabut; Stanislas Pol
Journal:  Dig Dis Sci       Date:  2020-04-18       Impact factor: 3.199

Review 8.  The oncologic burden of hepatitis C virus infection: A clinical perspective.

Authors:  Harrys A Torres; Terri Lynn Shigle; Nassim Hammoudi; James T Link; Felipe Samaniego; Ahmed Kaseb; Vincent Mallet
Journal:  CA Cancer J Clin       Date:  2017-07-06       Impact factor: 508.702

Review 9.  AGA Clinical Practice Update on Interaction Between Oral Direct-Acting Antivirals for Chronic Hepatitis C Infection and Hepatocellular Carcinoma: Expert Review.

Authors:  Amit G Singal; Joseph K Lim; Fasiha Kanwal
Journal:  Gastroenterology       Date:  2019-03-13       Impact factor: 22.682

10.  Occurrence and Recurrence of Hepatocellular Carcinoma After Successful Direct-Acting Antiviral Therapy for Patients With Chronic Hepatitis C Virus Infection.

Authors:  Sirisha Grandhe; Catherine T Frenette
Journal:  Gastroenterol Hepatol (N Y)       Date:  2017-07
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