首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Effectiveness and safety of didanosine, lamivudine and efavirenz versus zidovudine, lamivudine and efavirenz for the initial treatment of HIV-infected patients from the Spanish VACH cohort.
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Effectiveness and safety of didanosine, lamivudine and efavirenz versus zidovudine, lamivudine and efavirenz for the initial treatment of HIV-infected patients from the Spanish VACH cohort.

机译:地那洛辛,拉米夫定和依非韦伦与齐多夫定,拉米夫定和依非韦伦在西班牙VACH队列中的HIV感染患者的初始治疗中的有效性和安全性。

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BACKGROUND: Preliminary data suggest that a once-daily combination of lamivudine, didanosine and efavirenz is an effective alternative regimen for antiretroviral-naive HIV-1-infected patients. However, data from randomized trials comparing this combination versus standard first-line regimens are not available yet. In an observational study, we analyse the efficacy and tolerability of didanosine plus lamivudine and efavirenz versus zidovudine plus lamivudine and efavirenz in a cohort of therapy naive patients. METHODS: We performed an observational study on prospectively collected data from patients participating in a multicentre Spanish treatment-naive cohort (VACH cohort). Efficacy was assessed comparing time to therapeutic failure and CD4 cell recovery. Safety was analysed comparing the proportion of patients who discontinued therapy for toxicity or any other reason. RESULTS: Overall, 219 patients treated with once-daily didanosine/lamivudine/efavirenz and 409 patients receiving twice-daily zidovudine/lamivudine (Combivir) plus efavirenz were evaluated. By intent-to treat analysis (non-completers and therapeutic change=failure), time to treatment failure was similar in both groups of treatment: 40.0 months (95% CI 23.3-56.8 months) among patients on didanosine/lamivudine/efavirenz and 33.3 months (95% CI 25.6-41.1 months) in patients treated with zidovudine/lamivudine/efavirenz (P=0.253). The risk of failure due to treatment change was almost double among patients treated with zidovudine/lamivudine/efavirenz compared with those who received didanosine/lamivudine/efavirenz. CONCLUSIONS: Our data suggest that didanosine/lamivudine/efavirenz is a combination with an efficacy comparable to zidovudine/lamivudine/efavirenz as first-line therapy for HIV infection. The risk of treatment change was significantly higher among patients treated with zidovudine/lamivudine/efavirenz than in those starting therapy with didanosine/lamivudine/efavirenz.
机译:背景:初步数据表明,对于未经抗逆转录病毒治疗的HIV-1感染患者,拉米夫定,去羟肌苷和依非韦伦每天一次的组合是一种有效的替代方案。但是,尚无来自将这种组合与标准一线方案进行比较的随机试验数据。在一项观察性研究中,我们分析了在未接受过治疗的一组患者中,去羟肌苷加拉米夫定和依非韦伦与齐多夫定加拉米夫定和依非韦伦的疗效和耐受性。方法:我们进行了一项观察性研究,对来自多中心西班牙无治疗队列(VACH队列)的患者的前瞻性收集数据进行了观察。通过比较治疗失败的时间和CD4细胞的恢复来评估疗效。分析安全性,比较因毒性或任何其他原因而终止治疗的患者比例。结果:总体上,评估了每天使用一次地那松/拉米夫定/依非韦伦治疗的219例患者和每天两次使用齐多夫定/拉米夫定(Combivir)加依非韦伦的409例患者。通过意向治疗分析(未完成且治疗改变=失败),两组治疗失败的时间相似:使用去羟肌苷/拉米夫定/依非韦伦治疗的患者为40.0个月(95%CI为23.3-56.8个月),治疗率为33.3齐多夫定/拉米夫定/依非韦伦治疗的患者接受抗凝治疗的有效时间(95%CI 25.6-41.1个月)(P = 0.253)。与接受去羟肌苷/拉米夫定/依非韦伦治疗的患者相比,接受齐多夫定/拉米夫定/依非韦伦治疗的患者因治疗改变而失败的风险几乎翻倍。结论:我们的数据表明,去氧肌苷/拉米夫定/依非韦伦是一种组合物,其疗效可与齐多夫定/拉米夫定/依非韦伦相媲美,是治疗艾滋病毒的一线疗法。在接受齐多夫定/拉米夫定/依非韦伦治疗的患者中,治疗改变的风险显着高于开始用去羟肌苷/拉米夫定/依非韦伦治疗的患者。

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