Literature DB >> 26853230

Retreatment with sofosbuvir and simeprevir of patients with hepatitis C virus genotype 1 or 4 who previously failed a daclatasvir-containing regimen.

Christophe Hézode1,2, Stéphane Chevaliez2,3, Giovanna Scoazec1, Alexandre Soulier2,3, Anne Varaut1,2, Magali Bouvier-Alias2,3, Isaac Ruiz2,3, Françoise Roudot-Thoraval1,2, Ariane Mallat1,2, Cyrille Féray1,2, Jean-Michel Pawlotsky2,3.   

Abstract

UNLABELLED: Failure to achieve sustained virological response (SVR) with hepatitis C virus (HCV) direct-acting antiviral-based regimens is commonly associated with emergence of resistance-associated variants (RAVs). To avoid cross-resistance, recent guidelines recommend that patients who have failed on nonstructural protein 5A (NS5A) inhibitors should be retreated with sofosbuvir (SOF; NS5B inhibitor) combined with simeprevir (SIM; protease inhibitor [PI]); however, supporting evidence is lacking. This "real-world" study comprised patients who had failed to achieve SVR on previous NS5A-based therapy with daclatasvir (DCV) plus pegylated interferon (Peg-IFN) and ribavirin (RBV), with (n = 3) or without (n = 13) asunaprevir (ASV; PI). All 16 patients were retreated for 12 weeks with SOF plus SIM, without RBV. Antiviral efficacy was evaluated using the primary endpoint of SVR12 (SVR 12 weeks post-treatment); on-treatment response was also assessed. Patients (N = 16; 13 male; mean age: 54 years [range, 43-73]) were chronically infected with HCV genotype (GT) 1 (1a, n = 11; 1b, n = 3) or 4 (n = 2); they had advanced fibrosis or compensated cirrhosis (FibroScan, 9.6-70 kPa; cirrhosis, n = 9); median baseline HCV-RNA level was 1.38 × 10(6) IU/mL. No patient discontinued treatment because of adverse events or virological failure. All patients achieved HCV RNA below lower limit of quantification (<12 IU/mL) by end of treatment (EOT) and 10 of 16 had a rapid response (week 4). SVR12 was achieved by 14 of 16 patients; the remaining 2 relapsed by 4 weeks post-EOT (both were GT 1a infected with cirrhosis; 1 had previously failed DCV-ASV plus Peg-IFN and RBV). Presence of SIM RAVs/polymorphisms (R155K and Q80K) at study baseline did not predict retreatment failure.
CONCLUSION: Our findings support the concept of retreating NS5A inhibitor failures with SOF combined with SIM. However, the most difficult-to-cure patients may need more than 12 weeks of treatment and/or the addition of RBV. (Hepatology 2016;63:1809-1816).
© 2016 by the American Association for the Study of Liver Diseases.

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Year:  2016        PMID: 26853230     DOI: 10.1002/hep.28491

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  14 in total

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Authors:  Justin Taylor; Paula Cox-North; Charles S Landis
Journal:  Drugs       Date:  2016-12       Impact factor: 9.546

2.  Understanding Hepatitis C Virus Drug Resistance: Clinical Implications for Current and Future Regimens.

Authors:  David L Wyles; Anne F Luetkemeyer
Journal:  Top Antivir Med       Date:  2017 Jul/Aug

3.  Quadruple Therapy Offers High SVR Rates in Patients with HCV Genotype 4 with Previous Treatment Failure.

Authors:  Yousry Esam-Eldin Abo-Amer; Rehab Badawi; Mohamed El-Abgeegy; Heba Fadl Elsergany; Ahmed Abdelhaleem Mohamed; Sahar Mohamed Mostafa; Hatem Samir Alegaily; Shaimaa Soliman; Sally Elnawasany; Sherief Abd-Elsalam
Journal:  Adv Virol       Date:  2020-07-24

Review 4.  Resistance detection and re-treatment options in hepatitis C virus-related chronic liver diseases after DAA-treatment failure.

Authors:  Evangelista Sagnelli; Mario Starace; Carmine Minichini; Mariantonietta Pisaturo; Margherita Macera; Caterina Sagnelli; Nicola Coppola
Journal:  Infection       Date:  2018-08-06       Impact factor: 3.553

5.  Retreatment with sofosbuvir, ledipasvir, and add-on ribavirin for patients who failed daclatasvir and asunaprevir combination therapy.

Authors:  Goki Suda; Koji Ogawa; Yoshiya Yamamoto; Masaki Katagiri; Ken Furuya; Kenichi Kumagai; Jun Konno; Megumi Kimura; Naoki Kawagishi; Masatsugu Ohara; Machiko Umemura; Jun Ito; Takaaki Izumi; Masato Nakai; Takuya Sho; Mitsuteru Natsuizaka; Kenichi Morikawa; Akihito Tsubota; Noritomo Shimada; Etsuko Iio; Yasuhito Tanaka; Naoya Sakamoto
Journal:  J Gastroenterol       Date:  2017-03-18       Impact factor: 6.772

6.  Laparoscopic versus open liver resection for hepatocellular carcinoma: initial experience in Greece.

Authors:  Georgios C Sotiropoulos; Nikolaos Machairas; Paraskevas Stamopoulos; Ioannis D Kostakis; Dimitrios Dimitroulis; Dimitrios Mantas; Gregory Kouraklis
Journal:  Ann Gastroenterol       Date:  2016-06-24

Review 7.  Concise review: Interferon-free treatment of hepatitis C virus-associated cirrhosis and liver graft infection.

Authors:  Nina Weiler; Stefan Zeuzem; Martin-Walter Welker
Journal:  World J Gastroenterol       Date:  2016-11-07       Impact factor: 5.742

Review 8.  Management of direct antiviral agent failures.

Authors:  María Buti; Rafael Esteban
Journal:  Clin Mol Hepatol       Date:  2016-12-25

9.  Real-world cure rates for hepatitis C virus treatments that include simeprevir and/or sofosbuvir are comparable to clinical trial results.

Authors:  Kian Bichoupan; Neeta Tandon; James F Crismale; Joshua Hartman; David Del Bello; Neal Patel; Sweta Chekuri; Alyson Harty; Michel Ng; Keith M Sigel; Meena B Bansal; Priya Grewal; Charissa Y Chang; Jennifer Leong; Gene Y Im; Lawrence U Liu; Joseph A Odin; Nancy Bach; Scott L Friedman; Thomas D Schiano; Ponni V Perumalswami; Douglas T Dieterich; Andrea D Branch
Journal:  World J Virol       Date:  2017-11-12

10.  A 3-year follow-up study after treatment with simeprevir in combination with pegylated interferon-α and ribavirin for chronic hepatitis C virus infection.

Authors:  Fabien Zoulim; Christophe Moreno; Samuel S Lee; Peter Buggisch; Andrzej Horban; Eric Lawitz; Chris Corbett; Oliver Lenz; Bart Fevery; Thierry Verbinnen; Umesh Shukla; Wolfgang Jessner
Journal:  Virol J       Date:  2018-01-30       Impact factor: 4.099

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