Ebinuma Hirotoshi, Saito Hidetsugu, Tada Shinichiro, Nakamoto Nobuhiro, Kurita Satoshi, Kitamaura Kumi, Horikawa Hitomi, Kumagai Naoki, Tsuchimoto Kanji, Ishii Hiromasa, Hibi Toshifumi
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Hepatogastroenterology. 2006 Jan-Feb;53(67):94-9.
BACKGROUND/AIMS: Two distinct natural interferon-alpha (BALL-1 and Namalwa) are available for patients with chronic hepatitis C in Japan, but the efficacy has not been well documented. We investigated two studies using a natural BALL-1 interferon-alpha treatment for chronic hepatitis C and assessed its efficacy.
In interferon-alpha monotherapy (Study I), 42 patients with chronic hepatitis C received 10 mega units of BALL-1 interferon-alpha intramuscularly consecutively for an initial 2 weeks followed by three times a week for 6 months totally. In a combination therapy of natural interferon-alpha and interferon-beta (Study II), 24 patients received intravenous 3 mega units of interferon-beta twice daily for the initial 2 weeks followed by 10 mega units of natural BALL-1 interferon-alpha consecutively for 2 weeks and three times a week for 6 months totally. Efficacy and predictive factors for sustained viral response was investigated.
Study II included significant younger patients than study I. Sustained virological response was obtained in 31.0% in Study I and 56.5% in Study II by intention-to-treat analysis. Sustained viral response in the group of genotype 1b and viral load more than 100 KIU/mL was 3/23 (13.0%) and 8/18 (44.4%) in Study I and II, respectively. The response rate in Study II was higher than that of Study I especially among the patients with high pretreatment viral load or genotype 1b (p<0.05). Multivariate analysis showed that pre-treatment HCV-RNA levels, HCV-genotype, and histological staging before the interferon treatment were significant predictive factors of sustained viral response.
These studies suggest that natural BALL-1 interferon-alpha is useful for inducing sustained viral response in patients with chronic hepatitis C, even in those possessing genotype 1b and high viral load. In addition, the combination therapy with a starting regimen with twice-daily interferon-beta administration for 2 weeks may be more effective than monotherapy.
背景/目的:在日本,两种不同的天然α干扰素(BALL-1和Namalwa)可用于慢性丙型肝炎患者,但疗效尚未得到充分记录。我们开展了两项使用天然BALL-1α干扰素治疗慢性丙型肝炎的研究,并评估了其疗效。
在α干扰素单药治疗(研究I)中,42例慢性丙型肝炎患者连续2周每周一次肌肉注射10百万单位BALL-1α干扰素,随后6个月每周三次。在天然α干扰素与β干扰素联合治疗(研究II)中,24例患者在最初2周每天两次静脉注射3百万单位β干扰素,随后连续2周每周一次注射10百万单位天然BALL-1α干扰素,然后6个月每周三次。研究了持续病毒学应答的疗效和预测因素。
研究II中的患者比研究I中的患者明显年轻。意向性分析显示,研究I中持续病毒学应答率为31.0%,研究II中为56.5%。在研究I和II中,基因型1b且病毒载量超过100 KIU/mL组的持续病毒学应答率分别为3/23(13.0%)和8/18(44.4%)。研究II中的应答率高于研究I,尤其是在治疗前病毒载量高或基因型1b的患者中(p<0.05)。多变量分析显示,治疗前HCV-RNA水平、HCV基因型和干扰素治疗前的组织学分期是持续病毒学应答的重要预测因素。
这些研究表明,天然BALL-1α干扰素可有效诱导慢性丙型肝炎患者产生持续病毒学应答,即使是那些基因型为1b且病毒载量高的患者。此外,起始方案为连续2周每天两次注射β干扰素的联合治疗可能比单药治疗更有效。