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8 周达卡他韦-索磷布韦方案治疗慢性丙型肝炎的疗效:系统评价和荟萃分析。

Efficacy of 8-week daclatasvir-sofosbuvir regimen in chronic hepatitis C: a systematic review and meta-analysis.

机构信息

Clinical Pharmacy Department, College of Pharmacy, Cairo University, Cairo, 11562, Egypt.

出版信息

Virol J. 2024 Nov 4;21(1):275. doi: 10.1186/s12985-024-02544-2.

Abstract

BACKGROUND

The high rates of the sustained virologic response 12 weeks after treatment (SVR12) in real world settings provoked the adoption of shortened courses of the costly direct-acting antivirals (DAAs) regimens. This study provides, to our knowledge, the first systematic review and meta-analysis for the efficacy of the shortened 8-week course of sofosbuvir (SOF) plus daclatasvir (DCV), the most accessible DAAs in the low-middle income countries (LMICs).

METHODS

We performed a proportion meta-analysis to determine a reliable rate of SVR12 by pooling all studies that evaluated the results of the 8-week regimen of DCV + SOF. In addition, we applied sensitivity analyses using two imputation paradigms: a conservative approach, and a pragmatic approach to avoid overestimating the efficacy of the 8-week regimen in studies that followed a response-guided treatment (RGT) approach.

RESULTS

Six studies with a total of 159 patients were included. The pooled SVR12 rate ranged from 91 to 97% in the included scenarios. The pragmatic scenario showed that the pooled SVR12 was 97% (95% confidence interval (CI) 91%; 100%) with lower variability as assessed by the prediction interval. The conservative approach revealed an SVR12 of 93% (95% CI 84%; 95%).

CONCLUSION

The 8-week course of 60 mg DCV with SOF provided a comparable SVR12 to the standard 12-week regimen in treatment-naïve, non-HIV co-infected patients with a minimum estimated efficacy of 90%.

摘要

背景

在真实世界环境中,治疗后 12 周持续病毒学应答率(SVR12)较高,这促使人们采用更短疗程的昂贵直接作用抗病毒药物(DAA)方案。据我们所知,本研究首次对缩短疗程(8 周)的索磷布韦(SOF)联合达卡他韦(DCV)的疗效进行了系统评价和荟萃分析,这是中低收入国家(LMICs)最容易获得的 DAA。

方法

我们进行了比例荟萃分析,通过汇总所有评估 DCV+SOF 8 周方案结果的研究,确定 SVR12 的可靠率。此外,我们还应用了两种插补范式的敏感性分析:一种是保守方法,另一种是实用方法,以避免高估遵循应答指导治疗(RGT)方法的研究中 8 周方案的疗效。

结果

共有 6 项研究,总计 159 例患者纳入分析。在纳入的场景中,SVR12 的汇总率范围为 91%至 97%。实用情景表明,SVR12 的汇总率为 97%(95%置信区间 91%;100%),预测区间显示其变异性较低。保守方法显示 SVR12 为 93%(95%置信区间 84%;95%)。

结论

在未感染 HIV 的初治患者中,与标准的 12 周疗程相比,SOF 60mg DCV 的 8 周疗程提供了相当的 SVR12,其最低估计疗效为 90%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b7/11533316/4831fa04f6c8/12985_2024_2544_Fig1_HTML.jpg

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