首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Duration of first-line antiretroviral therapy with tenofovir and emtricitabine combined with atazanavir/ritonavir, efavirenz or lopinavir/ritonavir in the Italian ARCA cohort
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Duration of first-line antiretroviral therapy with tenofovir and emtricitabine combined with atazanavir/ritonavir, efavirenz or lopinavir/ritonavir in the Italian ARCA cohort

机译:替诺福韦和恩曲他滨联合阿扎那韦/利托那韦,依法韦仑或洛匹那韦/利托那韦联合一线抗逆转录病毒治疗的持续时间

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Objectives: To explore the durability of three first-line tenofovir/emtricitabine-based regimens in combination with atazanavir/ritonavir, efavirenz or lopinavir/ritonavir in HIV-1-infected patients. Patients and methods: A retrospective, longitudinal, multicentre analysis of adult patients enrolled in the Antiretroviral Resistance Cohort Analysis (ARCA), a national prospective observational cohort of HIV-1-infected patients followed up at more than 100 clinical and laboratory units in Italy. Patients eligible were those starting first-line antiretroviral therapy between 1 June 2004 and 15 April 2011 and who were followed up for at least 6 months. The primary endpoint was durability, defined as the time from antiretroviral therapy initiation to first treatment modification. Time-dependent events were analysed by the Kaplan-Meier approach and the Cox proportional hazard model. Results: There are 26 000 HIV-infected patients in the ARCA database, of whom 1654 met study inclusion criteria. Six hundred and thirty-nine (38.6%) received efavirenz, 321 (19.4%) received atazanavir/ritonavir and 694 (41.9%) received lopinavir/ritonavir as a first-line regimen. Over a total observation period of 88 months, equivalent to more than 2805 person-years of follow-up, 618 patients underwent treatment modification. Lopinavir/ritonavir, given twice daily, was associated with a higher discontinuation rate than efavirenz- and atazanavir-based regimens [hazard ratio (HR) 1.83, 95% confidence interval (CI) 1.56-2.15, P = 0.001]. Comparing the once-daily regimens, the rate of discontinuation of efavirenz was higher than that of atazanavir/ritonavir (HR 1.39, 95% CI 1.06-1.83, P = 0.016). Conclusions: Significant differences in treatment duration were observed among the three studied regimens. Once-daily regimens exhibited greater durability than the twice-daily regimen. Among the specific regimens examined, tenofovir/emtricitabine plus atazanavir/ritonavir showed the greatest durability.
机译:目的:探讨三种基于替诺福韦/恩曲他滨的一线治疗方案联合阿扎那韦/利托那韦,依非韦伦或洛匹那韦/利托那韦在HIV-1感染患者中的持久性。患者和方法:对参与抗逆转录病毒耐药性队列分析(ARCA)的成年患者进行回顾性,纵向,多中心分析,这是一个全国性的HIV-1感染患者前瞻性观察队列,在意大利的100多个临床和实验室部门进行了随访。符合条件的患者是在2004年6月1日至2011年4月15日之间开始一线抗逆转录病毒治疗的患者,并进行了至少6个月的随访。主要终点是持久性,定义为从抗逆转录病毒治疗开始到第一次治疗改变的时间。时间相关事件通过Kaplan-Meier方法和Cox比例风险模型进行了分析。结果:ARCA数据库中有26 000例HIV感染患者,其中1654符合研究纳入标准。一线方案有639例(38.6%)接受依非韦伦,321例(19.4%)接受阿扎那韦/利托那韦和694例(41.9%)接受洛匹那韦/利托那韦。在88个月的总观察期(相当于2805人-年的随访)中,对618例患者进行了治疗修改。每天服用两次洛匹那韦/利托那韦,与基于依非韦伦和阿扎那韦的方案相比,停用率更高[​​危险比(HR)1.83,95%置信区间(CI)1.56-2.15,P = 0.001]。比较每天一次的方案,依非韦伦的终止率高于阿扎那韦/利托那韦(HR 1.39,95%CI 1.06-1.83,P = 0.016)。结论:三种研究方案之间观察到治疗持续时间的显着差异。每天一次的方案比每天两次的方案显示出更大的持久性。在所检查的特定方案中,替诺福韦/恩曲他滨加阿扎那韦/利托那韦显示出最大的持久性。

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