4.7 Article

Randomized trial of low-dose peginterferon-2b plus low and escalating doses of ribavirin in older patients with chronic hepatitis C with high viral load genotype 1

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JOURNAL OF MEDICAL VIROLOGY
卷 87, 期 12, 页码 2082-2089

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WILEY
DOI: 10.1002/jmv.24276

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adverse event; dose modification; sustained virological response; treatment discontinuation

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Elderly patients with chronic hepatitis C cannot tolerate standard combination therapy of peginterferon and ribavirin, which remains the backbone of therapy in many countries, including Japan. The efficacy and safety of low-dose peginterferon -2b in combination with low and escalating doses of ribavirin in older patients with high viral load genotype 1 were investigated in this randomized controlled trial. Thirty-two patients (age 60 years) were randomized into standard (group 1) or low (group 2) doses of peginterferon -2b in combination with low and escalating doses of ribavirin. Patients were evaluated for safety and efficacy of treatment. There was a higher virological response rate in group 1 than in group 2. However, the response in men was higher than in women in the early treatment phase and 24 weeks after treatment (P=0.008). There was no significant difference between the two groups in the virological response rate in men and women. Completion of therapy was higher in group 2 than in group 1 (31% vs. 13%, P=0.200). Dose modification of ribavirin was less frequent in group 2 than in group 1 (69% vs. 88%, P=0.200). These data suggest that combination therapy with low-dose peginterferon plus low and escalating doses of ribavirin may be safer in older patients than that with standard dose peginterferon, without impairing the treatment response. J. Med. Virol. 87:2082-2089, 2015. (c) 2015 Wiley Periodicals, Inc.

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