Interferon-α plus indomethacin combined therapy in HBeAg positive chronic hepatitis B non-responder to a previous IFNα course: results of a pilot study

Pietro Andreone , Carmela Cursaro , Annagiulia Gramenzi , Rita Miniero , Mauro Bernardi , Giovanni Gasbarrini
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引用次数: 7

Abstract

Background: interferon-α is able to induce a sustained inhibition of hepatitis B virus replication in about 30–40% of patients with chronic hepatitis B. There is evidence that non-steroidal antiinflammatory drugs can enhance the synthesis of antiviral proteins induced by interferon-α, Aim: to evaluate the efficacy and tolerability of combined therapy with interferon-α plus indomethacin in HBeAg and HBV-DNA positive patients affected by chronic active hepatitis non-responders to a previous interferon-α treatment. Methods: after six months of retreatment with interferon-α (6 MU thrice weekly) six patients were enrolled, without stopping the therapy, to receive interferon-α (with the same schedule) plus indomethacin (25 mg orally twice daily) for an additional six month course. Results: at the end of treatment and after six months of follow-up alanine transaminase normalization was seen in three (50%) and four (66.7%) patients, HBV-DNA loss in one (17%) and three (50%), HBeAgHBeAb serum conversion in one (17%) and two (33%), respectively. The combined therapy was well tolerated and no indomethacin side-effects were observed. The treatment was stopped in one patient after 4 months because of a remarkable increase of alanine transaminase levels, and in another after five months because of hyperthyroidism occurrence. Conclusions: the results of this study, even if obtained in a small number of patients, are encouraging and suggest a randomized controlled trial to be confirmed.

干扰素α +吲哚美辛联合治疗对先前IFNα疗程无反应的HBeAg阳性慢性乙型肝炎:一项初步研究的结果
背景:干扰素-α能够在约30-40%的慢性乙型肝炎患者中诱导持续抑制乙型肝炎病毒的复制。有证据表明,非甾体类抗炎药物可以增强干扰素-α诱导的抗病毒蛋白的合成。评估干扰素-α联合吲哚美辛治疗HBeAg和HBV-DNA阳性慢性活动性肝炎患者对先前干扰素-α治疗无反应的疗效和耐受性。方法:6例患者接受干扰素-α (6 μ,每周3次)再治疗6个月后,在不停止治疗的情况下,接受干扰素-α(相同的治疗方案)加吲哚美辛(25 mg,口服,每日2次),再治疗6个月。结果:治疗结束和随访6个月后,丙氨酸转氨酶正常化3例(50%)和4例(66.7%),HBV-DNA丢失1例(17%)和3例(50%),HBeAgHBeAb血清转化1例(17%)和2例(33%)。联合用药耐受性良好,无吲哚美辛副作用。1例患者在治疗4个月后因丙氨酸转氨酶水平显著升高而停止治疗,另1例患者在治疗5个月后因甲状腺功能亢进而停止治疗。结论:这项研究的结果,即使是在少数患者中获得的,也是令人鼓舞的,并且表明一项随机对照试验有待证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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