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针对肝硬化患者的 HCV 靶向治疗。

HCV targeting of patients with cirrhosis.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

出版信息

J Hepatol. 2015 Oct;63(4):1015-22. doi: 10.1016/j.jhep.2015.06.003. Epub 2015 Jun 19.

Abstract

Interferon (IFN)-free treatments are now the treatment of choice for patients with chronic hepatitis C. Previously difficult to treat patients by IFN-containing treatments can now be treated safely by IFN-free therapies. More than 90% of hepatitis C genotype 1 and 4 patients with compensated cirrhosis or after orthotopic liver transplantation (OLT) can be cured by sofosbuvir combined with simeprevir, daclatasvir or ledipasvir, or by the paritaprevir/ritona-vir/ombitasvir/±dasabuvir (3D) combination. Addition of ribavirin confers to a minimal, if any, benefit to increase SVR. The need for ribavirin is controversial and remains to be studied. The optimal length of treatment is still unknown, and an individual approach may be needed. Most patients require only 12weeks of therapy. The safety of these drugs is not fully explored in patients with decompensated cirrhosis (Child-Pugh C), who should not be treated with protease inhibitors. In cirrhosis hepatitis C virus eradication does not necessarily mean a cure of the disease and patients regularly require follow-up. Drug-drug interactions with immunosuppressant in patients after OLT are easier to manage but still require attention. Better drugs are needed for genotype 3 patients.

摘要

无干扰素治疗方案现已成为慢性丙型肝炎患者的首选治疗方法。以前采用含干扰素治疗方案难以治疗的患者,现在可采用无干扰素疗法安全地进行治疗。对于丙型肝炎基因型 1 和 4 且代偿性肝硬化或肝移植(OLT)后的患者,可通过索非布韦联合simeprevir、达卡他韦或 ledipasvir,或通过 paritaprevir/ritonavir/ombitasvir/±dasabuvir(3D)联合方案治愈,治愈率超过 90%。添加利巴韦林对提高 SVR 几乎没有益处,即便有也极小。利巴韦林的使用仍存在争议,尚需进一步研究。最佳治疗时间尚不清楚,可能需要个体化治疗。大多数患者仅需 12 周的治疗。在失代偿性肝硬化(Child-Pugh C)患者中,这些药物的安全性尚未得到充分研究,不应使用蛋白酶抑制剂进行治疗。在肝硬化中,丙型肝炎病毒的清除并不一定意味着疾病的治愈,患者需要定期随访。OLT 后患者与免疫抑制剂的药物相互作用更容易管理,但仍需注意。对于基因型 3 患者,需要更好的药物。

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