Kim Hong Joo, Park Soo Kyung, Yang Hyo Joon, Jung Yoon Suk, Park Jung Ho, Park Dong Il, Cho Yong Kyun, Sohn Chong Il, Jeon Woo Kyu, Kim Byung Ik, Choi Kyu Yong
Division of Gastroenterology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Clin Mol Hepatol. 2016 Sep;22(3):350-358. doi: 10.3350/cmh.2016.0019. Epub 2016 Sep 25.
BACKGROUND/AIMS: To analyze the effects of preexisting lamivudine (LAM) resistance and applying antiviral treatment (adefovir [ADV] add-on LAM combination treatment) on long-term treatment outcomes, and comparing the clinical outcomes of antiviral-naïve chronic hepatitis B patients receiving entecavir (ETV) monotherapy.
This study enrolled 73 antiviral-naïve patients who received 0.5-mg ETV as an initial therapy and 54 patients who received ADV add-on LAM combination treatment as a rescue therapy from July 2006 to July 2010.
During 24-month treatments, the decreases in serum log10HBV-DNA values (copies/mL) were significantly greater in the antiviral-naïve patients treated with ETV than the patients receiving ADV add-on LAM combination treatment. The biochemical response rates for alanine aminotransferase normalization at 6 months (ETV) and 12 months (ADV add-on LAM) were 90.4% (66/73) and 77.8% (42/54), respectively (=0.048). A Kaplan-Meier analysis indicated that the rates of serologic response, viral breakthrough, and emergence of genotypic resistance did not differ significantly between the two patient groups. There were also no significant intergroup differences in the rates of disease progression (PD) and new development of hepatocellular carcinoma (HCC).
The long-term clinical outcomes of antiviral-naïve patients treated with ETV and LAM-resistant patients receiving ADV add-on LAM combination treatment were comparable in terms of the emergence of HCC and disease progression.
背景/目的:分析既往存在拉米夫定(LAM)耐药以及应用抗病毒治疗(阿德福韦酯[ADV]联合LAM治疗)对长期治疗结果的影响,并比较初治慢性乙型肝炎患者接受恩替卡韦(ETV)单药治疗的临床结局。
本研究纳入了2006年7月至2010年7月期间73例接受0.5mg ETV初始治疗的初治患者以及54例接受ADV联合LAM治疗作为挽救治疗的患者。
在24个月的治疗期间,接受ETV治疗的初治患者血清log10HBV-DNA值(拷贝/mL)的下降幅度显著大于接受ADV联合LAM治疗的患者。6个月时(ETV组)和12个月时(ADV联合LAM组)谷丙转氨酶正常化的生化应答率分别为90.4%(66/73)和77.8%(42/54)(=0.048)。Kaplan-Meier分析表明,两组患者的血清学应答率、病毒突破率和基因型耐药发生率无显著差异。两组间疾病进展(PD)率和肝细胞癌(HCC)新发病率也无显著差异。
在HCC发生和疾病进展方面,接受ETV治疗的初治患者与接受ADV联合LAM治疗的LAM耐药患者的长期临床结局相当。