Pegylated interferon α2a plus ribavirin versus pegylated interferon α2b plus ribavirin for the treatment of chronic hepatitis C in HIV-infected patients

被引:28
|
作者
Berenguer, J. [1 ]
Gonzalez-Garcia, J. [2 ]
Lopez-Aldeguer, J. [3 ]
Von-Wichmann, M. A. [4 ]
Quereda, C. [5 ]
Hernando, A. [6 ]
Sanz, J. [7 ]
Tural, C. [8 ]
Ortega, E. [9 ]
Mallolas, J. [10 ]
Santos, I. [11 ]
Miralles, P.
Montes, M. L. [2 ]
Bellon, J. M.
Esteban, H. [12 ]
机构
[1] Hosp Gen Gregorio Maranon, Unidad Enfermedades Infecciosas VIH 4100, Madrid 28007, Spain
[2] Hosp La Paz, Madrid, Spain
[3] Hosp La Fe, E-46009 Valencia, Spain
[4] Hosp Donostia, San Sebastian, Spain
[5] Hosp Ramon & Cajal, E-28034 Madrid, Spain
[6] Hosp 12 Octubre, E-28041 Madrid, Spain
[7] Hosp Principe Asturias, Alcala De Henares, Spain
[8] Hosp Badalona Germans Trias & Pujol, Badalona, Spain
[9] Hosp Gen Univ, Valencia, Spain
[10] Hosp Clin Barcelona, Barcelona, Spain
[11] Hosp La Princesa, Madrid, Spain
[12] Agencia Ensayos Clin Gesida, Madrid, Spain
关键词
comparative study; IFN; HCV; effectiveness; safety; infections; IMMUNODEFICIENCY-VIRUS-INFECTION; NATURAL-HISTORY; LIVER-DISEASE; PROGRESSION; COINFECTION; CIRRHOSIS; MORTALITY;
D O I
10.1093/jac/dkp106
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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-alpha 2a and peg-IFN-alpha 2b, both with ribavirin, against chronic hepatitis C virus (HCV) infection in HIV-infected patients. From the GESIDA HIV/HCV cohort, we analysed patients treated with peg-IFN-alpha 2a (n = 315) or peg-IFN-alpha 2b (n = 242). The primary endpoint was a sustained virological response (SVR). Both groups were well matched in baseline characteristics except for a higher frequency of injection drug users in the peg-IFN-alpha 2b group than in the peg-IFN-alpha 2a group (85% versus 76%; P = 0.01) and a higher frequency of bridging fibrosis and cirrhosis (F3-F4) in the peg-IFN-alpha 2b group than in the peg-IFN-alpha 2a group (42% versus 33%; P = 0.04). End-of-treatment response was significantly lower among patients treated with peg-IFN-alpha 2b [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-alpha 2b and those treated with peg-IFN-alpha 2a (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-alpha 2b and 47 (15%) patients treated with peg-IFN-alpha 2a. No differences in effectiveness and safety were found between peg-IFN-alpha 2b and peg-IFN-alpha 2a for the treatment of chronic HCV infection in HIV-infected patients.
引用
收藏
页码:1256 / 1263
页数:8
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