肝脏 ›› 2026, Vol. 31 ›› Issue (5): 635-638.

• 病毒性肝炎 • 上一篇    下一篇

恩替卡韦与替诺福韦酯治疗ALT正常慢性乙型肝炎患者的疗效与安全性比较

胡艳蓉, 陆佳赟, 孙舒, 尤虹, 钱先中   

  1. 214000 无锡 联勤保障部队第九〇四医院药剂科
  • 收稿日期:2025-11-19 发布日期:2026-07-10
  • 通讯作者: 钱先中,Email:qxzxi2004cosa@163.com

A comparison of the efficacy and safety of entecavir and tenofovir disoproxil fumarate treatment for chronic hepatitis B patients with normal ALT levels

HU Yan-rong, LU Jia-yun, SUN Shu, YOU Hong, QIAN Xian-zhong   

  1. Department of Pharmacy, No. 904 Hospital of the Joint Logistics Support Force, Wuxi 214000, China
  • Received:2025-11-19 Published:2026-07-10
  • Contact: QIAN Xian-zhong, Email: qxzxi2004cosa@163.com

摘要: 目的 比较恩替卡韦(ETV)与替诺福韦酯(TDF)治疗丙氨酸氨基转移酶(ALT)持续正常的慢性乙型肝炎(CHB)患者疗效及安全性。方法 回顾性分析2020年1月至2024年12个月联勤保障部队第九〇四医院收治的94例CHB患者临床资料,根据初始治疗方案分为ETV组(n=50)和TDF组(n=44)。比较两组病毒学应答指标、无创肝纤维化指标、免疫学应答及治疗12个月安全性指标。结果 TDF组达到完全病毒学应答(CVR)的时间短于ETV组,为6.0(5.0,10.0)个月比7.5(5.0,11.0)个月(P<0.05)。治疗12个月时,两组HBV DNA转阴率分别为84.1%比76.0%,CVR率分别为79.5%比72.0%,差异均无统计学意义(P>0.05);低病毒血症发生率分别为13.6%比14.0%,差异亦无统计学意义。免疫学应答方面,TDF组HBsAg下降≥0.3、≥0.5及≥1.0 lg IU/mL的比例均高于ETV组,为61.4%比40.0%、50.0%比28.0%、22.7%比8.0%,且HBsAg平均下降幅度更大,为(0.27±0.12)lg IU/mL比(0.18±0.09)lg IU/mL(P<0.05)。两组HBeAg阴转率差异无统计学意义。ETV组肾功能及骨代谢相关指标总体稳定;TDF组eGFR<90 mL/(min·1.73 m2)、蛋白尿及低磷血症发生率较高(均P<0.05),但未观察到严重不良事件。结论 TDF在早期病毒学应答及HBsAg下降方面具有一定优势,而ETV在长期安全性方面表现更为稳定。对于ALT正常的CHB患者,抗病毒治疗的启动及药物选择应结合病毒学获益与安全性进行个体化评估。

关键词: ALT正常慢性乙型肝炎, 恩替卡韦, 替诺福韦酯, 完全病毒学应答

Abstract: Objective To compare the efficacy and safety of entecavir (ETV) and tenofovir disoproxil fumarate (TDF) treatment for chronic hepatitis B (CHB) patients who have persistently normal serum alanine aminotransferase (ALT) levels, and to provide evidence for antiviral treatment strategies in this population. Methods The clinical data of 94 patients with CHB treated in No.904 Hospital of the Joint Logistics Support Force between January 2020 and December 2024 were retrospectively analyzed. According to the initial antiviral regimen, patients were divided into an ETV group (n=50) and a TDF group (n=44). Virological response parameters, noninvasive liver fibrosis indices, immunological responses, and safety outcomes at 12 months of treatment were compared between the two groups. Results The median time to achieve complete virological response (CVR) was shorter in the TDF group than that in the ETV group [6.0 (5.0, 10.0) months vs. 7.5 (5.0, 11.0) months, P<0.05]. At 12 months of treatment, there were no significant differences between the two groups in the rate of HBV DNA negativity (84.1% vs. 76.0%, P>0.05) or the CVR rate (79.5% vs. 72.0%, P>0.05). Similarly, no significant differences were observed in the incidence of low-level viremia (LLV) (13.6% vs. 14.0%, P>0.05) or the duration of LLV between the two groups. Regarding immunological response, the proportions of patients achieving HBsAg declines of ≥0.3, ≥0.5, and ≥1.0 lg IU/mL were significantly higher in the TDF group than those in the ETV group (61.4% vs. 40.0%, 50.0% vs. 28.0%, and 22.7% vs. 8.0%, respectively; all P<0.05), and the mean magnitude of HBsAg reduction was also greater in the TDF group [(0.27±0.12) lg IU/mL vs. (0.18±0.09) lg IU/mL, P<0.05]. No significant difference was observed in the HBeAg seroconversion rate between the two groups. The safety analysis showed that renal function and bone metabolism-related parameters remained generally stable in the ETV group, whereas the incidences of eGFR<90 mL/min/1.73 m2, proteinuria, and hypophosphatemia were higher those in the TDF group (all P<0.05); however, no serious adverse events were observed this group of patients. Conclusion Chronic hepatitis B patients with persistently normal ALT levels can effectively achieve virological suppression and hepatic benefits from antiviral therapy. TDF demonstrates certain advantages in early virological response and HBsAg decline, whereas ETV shows a more stable long-term safety profile. Initiation of antiviral therapy and selection of agents for CHB patients with normal ALT levels should be individualized by balancing virological benefits and safety considerations.

Key words: Chronic hepatitis B with normal ALT, Entecavir, Tenofovir disoproxil fumarate, Complete virological response