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HBV治疗逆转肝硬化 [复制链接]

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发表于 2013-2-6 13:23 |只看该作者 |倒序浏览 |打印
HBV Treatment Reverses CirrhosisNearly three quarters of hepatitis B virus–infected patients with cirrhosis at baseline were no longer cirrhotic after 5 years of tenofovir therapy.
Hepatitis B virus (HBV) is a common cause of cirrhosis, end-stage liver disease, and hepatocellular carcinoma, particularly in areas of the world where infection rates are high. Although short-term studies have shown that tenofovir and other antiviral drugs lead to improvement in liver histology, the effect of extended treatment on severe hepatic fibrosis or cirrhosis is less certain. Now, investigators have evaluated the effect of long-term tenofovir use on liver histology in a large number of HBV-infected patients.
Of 641 patients participating in double-blind, phase III trials comparing tenofovir with adefovir therapy for 48 weeks, 585 entered a manufacturer-sponsored, open-label study in which they were to receive 7 additional years of tenofovir therapy; 348 of these patients had liver biopsies performed at baseline and again after 240 weeks of treatment. Liver histology was improved in 87% of these patients at year 5; individuals with the most pretherapy liver injury showed the greatest improvement. Strikingly, of 96 patients with cirrhosis prior to treatment, 74% were no longer cirrhotic at year 5 of therapy. Patients with lower body-mass indexes were more likely to have fibrosis regression. Only 12 patients developed hepatocellular carcinoma, and only 2 developed decompensated liver disease. Virologic breakthrough was uncommon, and no resistance to tenofovir was detected.
Comment: This large trial demonstrates that long-term suppression of HBV replication results in improved liver histology, even in patients who have previously developed cirrhosis. The low rates of hepatocellular carcinoma and end-stage liver disease in patients receiving tenofovir suggest that effective antiviral therapy will lead to improved survival — as has recently been demonstrated in patients treated successfully for hepatitis C virus infection (JAMA 2012; 308:2584).
Rajesh T. Gandhi, MD
Published in Journal Watch Infectious Diseases January 9, 2013
Citation(s):

Marcellin P et al. Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: A 5-year open-label follow-up study. Lancet  2012 Dec 10;  [e-pub ahead of print]. (http://dx.doi.org/10.1016/S0140-6736(12)61425-1)

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发表于 2013-2-6 13:28 |只看该作者
HBV治疗逆转肝硬化

近四分之三的B型肝炎病毒感染在基线的肝硬化患者,替诺福韦治疗5年后不再是肝硬化。

乙型肝炎病毒(HBV)是肝硬化,终末期肝病,肝癌,特别是在地区感染率较高的世界里,一个常见的​​原因。虽然短期研究表明,替诺福韦和其他抗病毒药物导致肝组织学改善,严重的肝纤维化或肝硬化,延长治疗的效果不太确定。现在,调查人员已经评估了肝脏组织学上的长期替诺福韦使用了大量的HBV感染者。

的641例患者参加的双盲III期临床试验比较替诺福韦与阿德福韦治疗48周,585进入了一个制造商赞助的,开放标签研究中,他们分别额外获得7年的替诺福韦治疗,其中348例有肝活检在基线和240周的治疗后再次。肝组织学改善,87%的患者在5年;个人与治疗前肝损伤表现出最大的改善。引人注目的是,肝硬化治疗前的96例患者中,有74%已不再在5年的治疗肝硬化。身体质量指数较低的患者是可能有纤维化回归。只有12名患者发展为肝癌,只有2开发的失代偿性肝病。病毒学突破是罕见的,毫无抵抗能力和替诺福韦检测。

评论:这个大型试验表明,长期抑制HBV复制的结果,肝组织学改善,即使是在以前开发的肝硬化患者。肝癌和终末期肝病患者接受替诺福韦低利率的建议,有效的抗病毒治疗,会导致改善生存 - 已被证明在治疗的患者成功地为丙型肝炎病毒感染(JAMA 2012; 308:2584)。

- 拉杰什T.甘地,MD

2013年1月9日出版的杂志手表传染病
参考文献(S):

marcellin P等人。富马酸替诺福韦酯治疗慢性乙型肝炎肝硬化患者在治疗过程中的回归:一个5年的开放标签的随访研究。柳叶刀“杂志2012年12月10日[电子酒馆的提前打印]。 (http://dx.doi.org/10.1016/S0140-6736(12)61425-1)

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发表于 2013-2-6 15:36 |只看该作者
现时的抗病毒治疗对于肝硬化效果是肯定的,但对于肝癌还是没办法啊。

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发表于 2013-2-6 15:42 |只看该作者
回复 疯一点好 的帖子

如果能阻止肝纤维化的进展,应该大大降低肝癌的风险.不要等到肝硬化,可能为时已晚.

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神仙眷侣 如鱼得水 翡翠丝带 健康之翼

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发表于 2013-2-7 10:51 |只看该作者
回复 StephenW 的帖子

Stephen,ETV如何?
温故中知新

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发表于 2013-2-7 11:15 |只看该作者
回复 走遍四方 的帖子

同样有效.

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发表于 2013-2-7 12:43 |只看该作者
感谢分享
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