1.浙江大学医学院附属第一医院临床药学部,杭州 310003
2.杭州市临平区中西医结合医院药学部,杭州 311199
Received:14 October 2025,
Revised:2026-03-12,
Accepted:12 March 2026,
Published:15 April 2026
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钦佳怡,马葵芬,单文雅,等.4种治疗慢性乙型肝炎核苷(酸)类似物的临床综合评价 [J].中国药房,2026,37(07):859-863.
QIN Jiayi,MA Kuifen,SHAN Wenya,et al.Clinical comprehensive evaluation of four nucleoside (acid) analogues in the treatment of chronic hepatitis B[J].ZHONGGUO YAOFANG,2026,37(07):859-863.
钦佳怡,马葵芬,单文雅,等.4种治疗慢性乙型肝炎核苷(酸)类似物的临床综合评价 [J].中国药房,2026,37(07):859-863. DOI: 10.6039/j.issn.1001-0408.2026.07.06.
QIN Jiayi,MA Kuifen,SHAN Wenya,et al.Clinical comprehensive evaluation of four nucleoside (acid) analogues in the treatment of chronic hepatitis B[J].ZHONGGUO YAOFANG,2026,37(07):859-863. DOI: 10.6039/j.issn.1001-0408.2026.07.06.
目的
2
对恩替卡韦、富马酸替诺福韦二吡呋酯、富马酸丙酚替诺福韦、艾米替诺福韦4种已在我国上市的核苷(酸)类似物进行临床综合评价。
方法
2
基于《药品临床综合评价管理指南(2021年版 试行)》,检索中国知网、万方数据、维普网、PubMed、the Cochrane Library、Embase数据库及相关官网,收集4种药物的相关指南、共识及研究文献,结合药品说明书,从安全性、有效性、经济性、创新性、适宜性和可及性6个维度进行综合评价。
结果与结论
2
恩替卡韦的安全性、有效性、经济性、创新性、适宜性和可及性评分及综合评分分别为13、14、13、10、18、6、74分,富马酸替诺福韦二吡呋酯分别为13、17、18、8、18、7、81分,富马酸丙酚替诺福韦分别为14、20、12、8、18、5、77分,艾米替诺福韦分别为10.5、17、10、6、15、4、62.5分。富马酸替诺福韦二吡呋酯的综合评分最高,可作为优先推荐,适用于成人、儿童及妊娠期妇女,但需警惕肾功能损伤;富马酸丙酚替诺福韦为次选,适用于骨及肾脏高风险人群;恩替卡韦的综合评分与富马酸丙酚替诺福韦相近,需空腹用药并需根据患者肾功能调整剂量;艾米替诺福韦的评分最低,为弱推荐。临床需根据患者年龄、生理状态及风险因素等进行个体化用药。
OBJECTIVE
2
To conduct a comprehensive clinical evaluation of four nucleoside (acid) analogues that have been approved and marketed in China, such as entecavir, tenofovir disoproxil fumarate, tenofovir alafenamide fumarate, and tenofovir amibufenamide.
METHODS
2
According to
the Guideline for the Administration of Clinical Comprehensive Evaluation of Drugs
(2021 edition, trial implementation), a comprehensive search was conducted across databases including CNKI, Wanfang Data, VIP, PubMed, the Cochrane Library, Embase, as well as relevant official websites. Drug package inserts, guidelines, consensus statements, and relevant literature for the four drugs were collected and subjected to a comprehensive evaluation across six dimensions: safety, efficacy, cost-effectiveness, innovativeness, suitability, and accessibility.
RESULTS
2
The scores for entecavir in terms of safety, efficacy, cost-effectiveness, innovativeness, suitability, and accessibility-along with its comprehensive score-were 13, 14, 13, 10, 18, and 6, totaling 74 points. For tenofovir disoproxil fumarate, the respective scores were 13, 17, 18, 8, 18, and 7, totaling 81 points. For tenofovir alafenamide fumarate, the scores were 14, 20, 12, 8, 18, and 5, totaling 77 points. Finally, for tenofovir amibufenamide, the scores were 10.5, 17, 10, 6, 15, and 4, totaling 62.5 points.
CONCLUSIONS
2
Tenofovir disoproxil fumarate, with the highest score, is recommended as the first-line option, suitable for adults, children, and pregnant women. However, caution is warranted for potential renal impairment. Tenofovir alafenamide fumarate is recommended as a second-line alternative, particularly for individuals at high risk for bone and renal damage. Entecavir has a score similar to tenofovir alafenamide fumarate but requires dosing on an empty stomach and dose adjustment based on renal function of patients. Tenofovir amibufenamide received the lowest score and is considered a weak recommendation. The clinical application of these nucleoside (acid) analogues should be individualized based on the patient’s age, physiological status, and risk factors.
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