Liver Disease Prevention Center, Division of Gastroenterology and Hepatology, Jefferson Medical College, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA.
Expert Opin Pharmacother. 2010 Sep;11(13):2243-9. doi: 10.1517/14656566.2010.512437.
Hepatitis B virus (HBV) is a significant hepatocarcinogen. HBV replication is a major cause for the development of hepatocellular carcinoma (HCC). Past studies have documented that lamivudine (LAM) therapy deterred progression to cirrhosis and HCC. This risk reduction is attributed to effective viral suppression. There is a need for as many effective anti-HBV drugs as possible.
Telbivudine, the fourth FDA-approved oral antiviral drug, is highly potent for viral suppression for HBV. It is more potent than LAM and adefovir; its therapeutic response is superior to that of LAM in both HBeAg-positive and -negative patients, and it produces higher HBeAg seroconversion in patients with baseline ALT > or = 2 times normal. Telbivudine has a resistance rate lower than that of LAM and higher than that of entecavir or tenofovir.
There is a specific group of patients who are likely to achieve good therapeutic response with telbivudine.
Patients with low baseline HBV DNA combined with negative HBV DNA at week 24 obtain good therapeutic results with telbivudine. Therefore, selecting patients who meet the above conditions is important.
乙型肝炎病毒(HBV)是一种重要的肝癌致癌物。HBV 的复制是肝细胞癌(HCC)发展的主要原因。过去的研究已经证明,拉米夫定(LAM)治疗可以阻止肝硬化和 HCC 的进展。这种风险降低归因于有效的病毒抑制。需要尽可能多的有效抗 HBV 药物。
替比夫定,第四种获得 FDA 批准的口服抗病毒药物,对 HBV 的病毒抑制作用非常强。它比 LAM 和阿德福韦酯更有效;其治疗反应在 HBeAg 阳性和阴性患者中均优于 LAM,并且在基线 ALT >或= 2 倍正常值的患者中产生更高的 HBeAg 血清转换。替比夫定的耐药率低于 LAM,高于恩替卡韦或替诺福韦。
有一类特定的患者可能会从替比夫定治疗中获得良好的疗效。
基线 HBV DNA 低且第 24 周 HBV DNA 阴性的患者使用替比夫定可获得良好的治疗效果。因此,选择符合上述条件的患者非常重要。