Literature DB >> 26167694

Real-life experience with first generation HCV protease inhibitor therapy in Germany: The prospective, non-interventional PAN cohort.

S Mauss1, K Böker2, P Buggisch3, S Christensen4, W P Hofmann5, E Schott6, H Pfeiffer-Vornkahl7, U Alshuth8, D Hüppe9.   

Abstract

BACKGROUND AND AIMS: The efficacy and safety of peginterferon alfa-2a (PEG-IFN) plus ribavirin (RBV) and either boceprevir (BOC) or telaprevir (TVR), and physician adherence to treatment algorithms were evaluated in patients included in an ongoing non-interventional study (PAN) enrolling adults with chronic hepatitis C virus (HCV) infection managed in German office-based practices.
METHODS: The analysis included HCV genotype 1-infected, treatment-naïve and treatment-experienced patients treated with BOC or TVR. Demographic, treatment history, virological response, safety, and patient management data were collected.
RESULTS: Of a total 1087 patients, 58.1 % achieved sustained virological responses (SVR). Response rates were higher in treatment-naïve (BOC 55 %; TVR 63.4 %) and prior relapse patients (BOC 63.2 %; TVR 74.5 %) versus previous null-responders (BOC 14.3 %; TVR 25 %). The most commonly reported adverse event overall was fatigue (60.6 %); 45.8 % patients experienced hemoglobin < 10 g/dL. Patients with cirrhosis had lower rates of SVR versus those without (42.9 % vs. 60.7 %, respectively), and had a higher incidence of serious adverse events (SAEs) (16.7 % vs. 8.6 %, respectively) and treatment discontinuation (44.6 % vs. 25.2 %, respectively). According to recommended response-guided treatment algorithms, about 70 % of patients were managed appropriately, 11/10 % (BOC/TVR) received unnecessarily extended therapy, and 19/7 % (BOC/TVR) received inappropriately shortened therapy.
CONCLUSIONS: The efficacy and safety of BOC- and TVR-based triple therapy in this large, "real-world" cohort were largely comparable to that reported in pivotal clinical trials, although SVR rates were lower overall. Recommended futility or treatment extension rules were violated in a substantial proportion of patients with potential implications for response, adverse events and costs. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2015        PMID: 26167694     DOI: 10.1055/s-0034-1399383

Source DB:  PubMed          Journal:  Z Gastroenterol        ISSN: 0044-2771            Impact factor:   2.000


  6 in total

1.  Efficacy and safety profile of boceprevir- or telaprevir-based triple therapy or dual peginterferon alfa-2a or alfa-2b plus ribavirin therapy in chronic hepatitis C: the real-world PegBase observational study.

Authors:  Alessandra Mangia; Graham R Foster; Christoph P Berg; Manuela Curescu; Victor De Ledinghen; François Habersetzer; Spilios Manolakopoulos; Elisa Negri; George Papatheodoridis; Silke Ahlers; Marco Castillo; Georgios Bakalos; Stefan Mauss
Journal:  Ann Gastroenterol       Date:  2017-03-23

2.  Effectiveness and safety of first-generation protease inhibitors in real-world patients with hepatitis C virus genotype 1 infection in Brazil: a multicenter study.

Authors:  Luciana Azevedo Callefi; Cristiane Alves Villela-Nogueira; Simone de Barros Tenore; Dimas Carnaúba-Júnior; Henrique Sérgio Moraes Coelho; Paulo de Tarso A Pinto; Letícia Cancella Nabuco; Mário Guimarães Pessoa; Maria Lucia Cardoso Gomes Ferraz; Paulo Roberto Abrão Ferreira; Ana de Lourdes Candolo Martinelli; Silvana Gama Florencio Chachá; Adalgisa de Souza Paiva Ferreira; Alessandra Porto de Macedo Bisio; Carlos Eduardo Brandão-Mello; Mário Reis Álvares-Da-Silva; Tânia Reuter; Claudia Alexandra Pontes Ivantes; Renata de Mello Perez; Maria Cássia Jacintho Mendes-Correa
Journal:  Clinics (Sao Paulo)       Date:  2017-06       Impact factor: 2.365

3.  Effectiveness of triple therapy with direct-acting antivirals for hepatitis C genotype 1 infection: application of propensity score matching in a national HCV treatment registry.

Authors:  Emma Gray; David J Pasta; Suzanne Norris; Aisling O'Leary
Journal:  BMC Health Serv Res       Date:  2017-04-19       Impact factor: 2.655

4.  Economic study of the value of expanding HCV treatment capacity in Germany.

Authors:  Urbano Sbarigia; Daniel Wirth; Karen Van Nuys; Caroline Huber; Ron Brookmeyer; Jona Stahmeyer; Christian Krauth
Journal:  BMJ Open Gastroenterol       Date:  2017-04-04

5.  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

6.  Outcomes and Costs of Treating Hepatitis C Patients in the Era of First Generation Protease Inhibitors - Results from the PAN Study.

Authors:  Jona T Stahmeyer; Siegbert Rossol; Florian Bert; Klaus H W Böker; Harald-Robert Bruch; Christoph Eisenbach; Ralph Link; Christine John; Stefan Mauss; Renate Heyne; Eckart Schott; Heike Pfeiffer-Vornkahl; Dietrich Hüppe; Christian Krauth
Journal:  PLoS One       Date:  2016-07-28       Impact factor: 3.240

  6 in total

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