PMID- 27095760 OWN - NLM STAT- MEDLINE DCOM- 20170926 LR - 20181202 IS - 1007-3418 (Print) IS - 1007-3418 (Linking) VI - 24 IP - 3 DP - 2016 Mar 20 TI - [Clinical efficacy of pegylated interferon in patients co-infected with HIV and HCV who failed standard interferon therapy]. PG - 181-5 LID - 10.3760/cma.j.issn.1007-3418.2016.03.005 [doi] AB - OBJECTIVE: To investigate the efficacy and safety of pegylated interferon-alpha (PEG-INF-alpha) combined with ribavirin in patients co-infected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) who failed prior standard interferon therapy. METHODS: A prospective study was performed to analyze HCV RNA load, liver function, and CD4+ count at weeks 0 (baseline), 12, 24, and 48 of treatment and at 24 weeks after drug discontinuation in 20 patients co-infected with HIV and HCV who failed standard interferon therapy and were then treated with PEG-INF-alphaand ribavirin. RESULTS: Among the 20 patients, 14 were infected with HCV genotype 1b, 3 with HCV genotype 2a, and 3 failed sequencing. At baseline, the mean CD4(+)count, mean CD8(+)count, and mean CD4(+)/CD8(+)ratio were 406.45 +/- 210.83 cells/ml, 1 076.45 +/- 716.18 cells /ml, and 0.43 +/- 0.17, respectively; the mean HCV RNA load was 6.01 +/- 1.13 log10IU/ml; 12 patients (60%) had abnormal liver function. A total of 14 patients (70%) achieved complete early virologic response, 15 (75%) achieved end-of-treatment virologic response, 7 (35%) achieved sustained virologic response (SVR), and 8 (40%) experienced recurrence. The incidence rate of drug-related adverse events during the treatment was 50% (10/20); no serious adverse events occurred, and no patient withdrew from the treatment due to adverse events. At week 48, both CD4(+)and CD8(+)counts of all patients declined significantly compared with the baseline values (P= 0.001 and 0.001), but the CD4(+)/CD8(+)ratio increased significantly (P= 0.032). The SVR group had a significantly lower mean baseline HCV RNA load than the non-SVR group (4.95 +/- 1.18 log10IU/ml vs 6.59 +/- 0.53 log10IU/ml,t= 3.49,P= 0.009). CONCLUSION: In the patients co-infected with HIV and HCV who failed standard interferon therapy, PEG-INF-alphacombined with ribavirin has good efficacy and safety, and the patients with a low baseline HCV RNA load are more likely to achieve SVR. FAU - Ke, Y C AU - Ke YC AD - Department of Infectious Diseases, Guangzhou No.8 People's Hospital Affiliated to Guangzhou Medical University, Guangzhou 510060, China. FAU - Li, L H AU - Li LH FAU - Hu, F Y AU - Hu FY FAU - He, Y AU - He Y FAU - Lan, Y AU - Lan Y FAU - Chen, X J AU - Chen XJ FAU - Tang, X P AU - Tang XP FAU - Cai, W P AU - Cai WP LA - chi PT - Journal Article PL - China TA - Zhonghua Gan Zang Bing Za Zhi JT - Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology JID - 9710009 RN - 0 (Anti-Retroviral Agents) RN - 0 (Antiviral Agents) RN - 0 (Interferon-alpha) RN - 0 (RNA, Viral) RN - 49717AWG6K (Ribavirin) SB - IM MH - Anti-Retroviral Agents/therapeutic use MH - Antiviral Agents/*therapeutic use MH - CD4 Lymphocyte Count MH - Coinfection MH - Drug Therapy, Combination MH - Female MH - HIV Infections/*complications/drug therapy/virology MH - Hepacivirus/classification/drug effects/isolation & purification MH - Hepatitis C, Chronic/complications/*drug therapy/virology MH - Humans MH - Immunotherapy MH - Interferon-alpha/adverse effects/*therapeutic use MH - Male MH - Prospective Studies MH - RNA, Viral/blood MH - Recurrence MH - Ribavirin/adverse effects/*therapeutic use MH - Standard of Care MH - Sustained Virologic Response MH - Treatment Outcome MH - Viral Load EDAT- 2016/04/21 06:00 MHDA- 2017/09/28 06:00 CRDT- 2016/04/21 06:00 PHST- 2016/04/21 06:00 [entrez] PHST- 2016/04/21 06:00 [pubmed] PHST- 2017/09/28 06:00 [medline] AID - 10.3760/cma.j.issn.1007-3418.2016.03.005 [doi] PST - ppublish SO - Zhonghua Gan Zang Bing Za Zhi. 2016 Mar 20;24(3):181-5. doi: 10.3760/cma.j.issn.1007-3418.2016.03.005.