OBJECTIVES: The two currently available types of pegylated interferon (peg-IFN) used to treat hepatitis C have different pharmacokinetic properties. It is unclear how these differences affect response to therapy. We compared the effectiveness and safety of peg-IFN-alpha2a and peg-IFN-alpha2b, both with ribavirin, against chronic hepatitis C virus (HCV) infection in HIV-infected patients. METHODS: From the GESIDA HIV/HCV cohort, we analysed patients treated with peg-IFN-alpha2a (n = 315) or peg-IFN-alpha2b (n = 242). The primary endpoint was a sustained virological response (SVR). RESULTS: Both groups were well matched in baseline characteristics except for a higher frequency of injection drug users in the peg-IFN-alpha2b group than in the peg-IFN-alpha2a group (85% versus 76%; P = 0.01) and a higher frequency of bridging fibrosis and cirrhosis (F3-F4) in the peg-IFN-alpha2b group than in the peg-IFN-alpha2a group (42% versus 33%; P = 0.04). End-of-treatment response was significantly lower among patients treated with peg-IFN-alpha2b [40% versus 52%; odds ratio (OR), 1.63; 95% confidence interval (95% CI), 1.16-2.29; P < 0.01]. However, no significant differences were found in SVR between patients treated with peg-IFN-alpha2b and those treated with peg-IFN-alpha2a (31% versus 33%; OR, 1.09; 95% CI, 0.75-1.59; P = 0.655). Therapy was interrupted due to adverse events in 33 (14%) patients treated with peg-IFN-alpha2b and 47 (15%) patients treated with peg-IFN-alpha2a. CONCLUSIONS: No differences in effectiveness and safety were found between peg-IFN-alpha2b and peg-IFN-alpha2a for the treatment of chronic HCV infection in HIV-infected patients.
OBJECTIVES: The two currently available types of pegylated interferon (peg-IFN) used to treat hepatitis C have different pharmacokinetic properties. It is unclear how these differences affect response to therapy. We compared the effectiveness and safety of peg-IFN-alpha2a and peg-IFN-alpha2b, both with ribavirin, against chronic hepatitis C virus (HCV) infection in HIV-infectedpatients. METHODS: From the GESIDA HIV/HCV cohort, we analysed patients treated with peg-IFN-alpha2a (n = 315) or peg-IFN-alpha2b (n = 242). The primary endpoint was a sustained virological response (SVR). RESULTS: Both groups were well matched in baseline characteristics except for a higher frequency of injection drug users in the peg-IFN-alpha2b group than in the peg-IFN-alpha2a group (85% versus 76%; P = 0.01) and a higher frequency of bridging fibrosis and cirrhosis (F3-F4) in the peg-IFN-alpha2b group than in the peg-IFN-alpha2a group (42% versus 33%; P = 0.04). End-of-treatment response was significantly lower among patients treated with peg-IFN-alpha2b [40% versus 52%; odds ratio (OR), 1.63; 95% confidence interval (95% CI), 1.16-2.29; P < 0.01]. However, no significant differences were found in SVR between patients treated with peg-IFN-alpha2b and those treated with peg-IFN-alpha2a (31% versus 33%; OR, 1.09; 95% CI, 0.75-1.59; P = 0.655). Therapy was interrupted due to adverse events in 33 (14%) patients treated with peg-IFN-alpha2b and 47 (15%) patients treated with peg-IFN-alpha2a. CONCLUSIONS: No differences in effectiveness and safety were found between peg-IFN-alpha2b and peg-IFN-alpha2a for the treatment of chronic HCV infection in HIV-infectedpatients.
Authors: Luis F López-Cortés; Rosa Ruiz-Valderas; Luis Jimenez-Jimenez; María F González-Escribano; Almudena Torres-Cornejo; Rosario Mata; Antonio Rivero; Juan A Pineda; Manuel Marquez-Solero; Pompeyo Viciana Journal: PLoS One Date: 2012-01-03 Impact factor: 3.240
Authors: M Vogel; G Ahlenstiel; B Hintsche; S Fenske; A Trein; T Lutz; D Schürmann; C Stephan; P Khaykin; M Bickel; C Mayr; A Baumgarten; P Buggisch; H Klinker; C John; J Gölz; S Staszewski; J K Rockstroh Journal: Eur J Med Res Date: 2010-03-30 Impact factor: 2.175
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Authors: Juan Berenguer; Ángela Gil-Martin; Inmaculada Jarrin; Ana Moreno; Lourdes Dominguez; Marisa Montes; Teresa Aldámiz-Echevarría; María J Téllez; Ignacio Santos; Laura Benitez; José Sanz; Pablo Ryan; Gabriel Gaspar; Beatriz Alvarez; Juan E Losa; Rafael Torres-Perea; Carlos Barros; Juan V San Martin; Sari Arponen; María T de Guzmán; Raquel Monsalvo; Ana Vegas; María T Garcia-Benayas; Regino Serrano; Luis Gotuzzo; María Antonia Menendez; Luis M Belda; Eduardo Malmierca; María J Calvo; Encarnación Cruz-Martos; Juan J González-García Journal: Hepatology Date: 2018-04-27 Impact factor: 17.425