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替诺福韦艾拉酚胺治疗慢性乙型肝炎的长期真实世界结局:初治和经治患者的详细分析

Long-Term Real-World Outcomes of Tenofovir Alafenamide in Chronic Hepatitis B: Detailed Analysis of Treatment-Naive and Experienced Patients.

作者信息

Song Yu-Xuan, Song Guang-Jun, Ma Hui, Feng Bo, Xie Yan-Di

机构信息

Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Beijing International Cooperation Base for Science and Technology on NAFLD Diagnosis, Beijing, China.

出版信息

Korean J Gastroenterol. 2025 Jan 25;85(1):64-72. doi: 10.4166/kjg.2024.140.

Abstract

BACKGROUND/AIMS: This study assessed the long-term efficacy and safety of tenofovir alafenamide (TAF) in real-world settings.

METHODS

Patients who were candidates for TAF treatment and were followed up at 12-week intervals over 192 weeks were enrolled in this study.

RESULTS

One hundred and forty-four patients (50 treatment-naive and 94 treatment-experienced) were included in this study. The cumulative incidence rates of cirrhosis and hepatocellular carcinoma at 192 weeks were 3.9% and 0.7%, respectively. In treatment- naive patients, the rates of a virological response, HBeAg conversion, and HBsAg loss at 192 weeks were 100%, 33.3%, and 2%, respectively. The treatment-naive patients exhibited higher baseline HBsAg levels than the treatment-experienced patients (4.31 logIU/mL vs. 3.97 logIU/mL). A significant decrease in the HBsAg levels from the baseline was observed at 144 and 192 weeks in the treatment-naive patients (p=0.01). The baseline body mass index (BMI) <25 kg/m (p=0.02) and HBsAg <3.3 logIU/mL (p=0.04) were identified as predictive factors for a decrease in HBsAg ≥0.5 logIU/mL at 48 weeks. The eGFR levels were consistently lower in the treatment-experienced patients throughout the study. Although the treatment-naive patients showed no abnormal increases in urinary URBP, the treatment-experienced patients showed elevated urinary 2MG and NAG levels at the baseline, which decreased over the treatment course. The total cholesterol, triglyceride, and low-density lipoprotein levels were similar in both groups.

CONCLUSIONS

Prolonging the TAF treatment duration enhances the virological response rate. The decline in HBsAg levels was more significant in the treatment-naive patients than in the treatment-experienced patients. The baseline BMI <25 kg/m and HBsAg <3.3 logIU/mL were predictive factors for a significant decline in HBsAg at 48 weeks. TAF has high renal safety and no significant impact on lipid levels.

摘要

背景/目的:本研究评估了替诺福韦艾拉酚胺(TAF)在实际临床环境中的长期疗效和安全性。

方法

本研究纳入了符合TAF治疗条件且在192周内每隔12周进行随访的患者。

结果

本研究共纳入144例患者(50例初治患者和94例经治患者)。192周时肝硬化和肝细胞癌的累积发生率分别为3.9%和0.7%。在初治患者中,192周时病毒学应答率、HBeAg血清学转换率和HBsAg消失率分别为100%、33.3%和2%。初治患者的基线HBsAg水平高于经治患者(4.31 logIU/mL对3.97 logIU/mL)。在初治患者中,144周和192周时观察到HBsAg水平较基线有显著下降(p=0.01)。基线体重指数(BMI)<25 kg/m²(p=0.02)和HBsAg<3.3 logIU/mL(p=0.04)被确定为48周时HBsAg下降≥0.5 logIU/mL的预测因素。在整个研究过程中,经治患者的估算肾小球滤过率(eGFR)水平持续较低。虽然初治患者的尿视黄醇结合蛋白(URBP)没有异常升高,但经治患者在基线时尿β2微球蛋白(2MG)和N-乙酰-β-D-氨基葡萄糖苷酶(NAG)水平升高,在治疗过程中下降。两组的总胆固醇、甘油三酯和低密度脂蛋白水平相似。

结论

延长TAF治疗时间可提高病毒学应答率。初治患者的HBsAg水平下降比经治患者更显著。基线BMI<25 kg/m²和HBsAg<3.3 logIU/mL是48周时HBsAg显著下降的预测因素。TAF具有较高的肾脏安全性,对血脂水平无显著影响。

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