PMID- 23396736 OWN - NLM STAT- MEDLINE DCOM- 20131017 LR - 20190919 IS - 1665-2681 (Print) IS - 1665-2681 (Linking) VI - 12 IP - 2 DP - 2013 Mar-Apr TI - Addition of pentoxifylline to pegylated interferon-alpha-2a and ribavirin improves sustained virological response to chronic hepatitis C virus: a randomized clinical trial. PG - 248-55 AB - BACKGROUND AND AIM: The commonly accepted treatment for hepatitis C virus (HCV) infection, pegylated interferon alpha (PEG INF-alpha) and ribavirin, leads to 50-60% of sustained virological response (SVR). On the other hand, pentoxifylline (PTX) possesses antiviral and hepatoprotector properties. AIM: To investigate whether the addition of PTX to conventional hepatitis C treatment increases SVR. MATERIAL AND METHODS: Seventy two patients of both genders were studied in a randomized fashion; the diagnosis of chronic HCV infection was made according to clinical and laboratory criteria and histopathologically classified according to METAVIR scoring system criteria. HCV viral load was tested by PCR, baseline, and after 6 months of treatment, as well as anti-HCV, anti-hepatitis B virus , and anti-human immunodeficiency virus antibodies by enzyme-linked immunosorbent assay. During 48 weeks, control group patients were treated with PEG INF-alpha- 2a plus ribavirin. PTX was administered to Experimental Group patients prior to the treatment. RESULTS: Demographic data were similar in both groups. Experimental- and control-group subjects were at F2 and F3 states according to the METAVIR classification. The most common HCV genotypes were 1a and 1b (39% in the control group in each case, and 42% in the experimental group in each case). At the end of the study, hepatic enzymes and viral load decreased in both groups to similar values. SVR in the experimental group increased significantly (p < 0.05) when compared with standard therapy alone. CONCLUSION: Addition of PTX to conventional chronic hepatitis C treatment may increase the percentage of patients with SVR. FAU - Jimenez-Luevano, Miguel Angel AU - Jimenez-Luevano MA AD - Servicio de Gastroenterologia, Hospital Valentin Gomez Farias, Instituto de Seguridad y Seguro Social de los Trabajadores del Estado (ISSSTE), Zapopan, Jalisco, Mexico. FAU - Lerma-Diaz, Jose Manuel AU - Lerma-Diaz JM FAU - Hernandez-Flores, Georgina AU - Hernandez-Flores G FAU - Jimenez-Partida, Miguel Angel AU - Jimenez-Partida MA FAU - Bravo-Cuellar, Alejandro AU - Bravo-Cuellar A LA - eng PT - Journal Article PT - Randomized Controlled Trial PL - Mexico TA - Ann Hepatol JT - Annals of hepatology JID - 101155885 RN - 0 (Antiviral Agents) RN - 0 (Biomarkers) RN - 0 (Hepatitis C Antibodies) RN - 0 (Interferon-alpha) RN - 0 (Recombinant Proteins) RN - 3WJQ0SDW1A (Polyethylene Glycols) RN - 49717AWG6K (Ribavirin) RN - Q46947FE7K (peginterferon alfa-2a) RN - SD6QCT3TSU (Pentoxifylline) SB - IM MH - Adult MH - Aged MH - Antiviral Agents/adverse effects/*therapeutic use MH - Biomarkers/blood MH - Chi-Square Distribution MH - Drug Therapy, Combination MH - Enzyme-Linked Immunosorbent Assay MH - Female MH - Hepacivirus/genetics/immunology MH - Hepatitis C Antibodies/blood MH - Hepatitis C, Chronic/blood/diagnosis/*drug therapy MH - Humans MH - Interferon-alpha/adverse effects/*therapeutic use MH - Male MH - Mexico MH - Middle Aged MH - Pentoxifylline/adverse effects/*therapeutic use MH - Pilot Projects MH - Polyethylene Glycols/adverse effects/*therapeutic use MH - Polymerase Chain Reaction MH - Predictive Value of Tests MH - Prospective Studies MH - Recombinant Proteins/adverse effects/therapeutic use MH - Ribavirin/adverse effects/*therapeutic use MH - Time Factors MH - Treatment Outcome MH - Viral Load EDAT- 2013/02/12 06:00 MHDA- 2013/10/18 06:00 CRDT- 2013/02/12 06:00 PHST- 2013/02/12 06:00 [entrez] PHST- 2013/02/12 06:00 [pubmed] PHST- 2013/10/18 06:00 [medline] AID - S1665-2681(19)31363-8 [pii] PST - ppublish SO - Ann Hepatol. 2013 Mar-Apr;12(2):248-55.