Flandre P, Pugliese P, Allavena C, Katlama C, Cotte L, Cheret A, Cabié A, Rey D, Chirouze C, Bani-Sadr F, Cuzin L
INSERM, UMR-S 1136, Paris, France.
Pierre Louis Institute of Epidemiology and Public Health, Sorbonne Universities, UPMC Université de Paris 06, Paris, France.
HIV Med. 2016 May;17(5):380-4. doi: 10.1111/hiv.12306. Epub 2015 Aug 26.
To compare the efficacy, in current clinical practice, of first regimens containing abacavir with lamivudine (ABC/3TC) or tenofovir with emtricitabine (TDF/FTC) in patients with baseline viral load ≥100,000 HIV-1 RNA copies/mL.
Using a prospective cohort, we selected all patients starting a first HIV regimen based either on ABC/3TC or on TDF/FTC. The propensity score (PS) method was used to limit the indication bias due to the observational nature of the data. Adjusting and weighting methods via PS were used to compare the effectiveness of a first regimen containing ABC/3TC or TDF/FTC. The primary outcome was treatment failure by month 12 (M12).
Overall, 2781 patients started an antiretroviral (ARV) regimen with ABC/3TC or TDF/FTC each in combination with efavirenz, boosted atazanavir or boosted darunavir. Among the 2472 uncensored patients before M12, 962 (39%) had a baseline viral load ≥100,000 copies/mL of whom 294 were in treatment failure at or before M12. Our analyses showed no difference between ABC/3TC and TDF/FTC in the risk of treatment failure at M12 in patients starting an ARV regimen with a high viral load (≥100,000 copies/mL).
Using a large prospectively collected cohort of patients seeking care in France, we found no evidence that ABC/3TC based regimens led to more failures than TDF/FTC based ones in patients with high baseline viral loads.
在当前临床实践中,比较含阿巴卡韦与拉米夫定(ABC/3TC)的初始方案或替诺福韦与恩曲他滨(TDF/FTC)的初始方案对基线病毒载量≥100,000 HIV-1 RNA拷贝/mL患者的疗效。
采用前瞻性队列研究,我们选择了所有开始基于ABC/3TC或TDF/FTC的首个HIV治疗方案的患者。倾向评分(PS)方法用于限制因数据的观察性而导致的指征偏倚。通过PS的调整和加权方法用于比较含ABC/3TC或TDF/FTC的首个方案的有效性。主要结局是第12个月(M12)时的治疗失败。
总体而言,2781例患者开始使用ABC/3TC或TDF/FTC与依非韦伦、增强型阿扎那韦或增强型达芦那韦联合的抗逆转录病毒(ARV)方案。在M12之前的2472例未删失患者中,962例(39%)基线病毒载量≥100,000拷贝/mL,其中294例在M12或之前出现治疗失败。我们的分析显示,对于开始使用高病毒载量(≥100,000拷贝/mL)ARV方案的患者,ABC/3TC和TDF/FTC在M12时的治疗失败风险上没有差异。
通过对在法国接受治疗的大量前瞻性收集的患者队列进行研究,我们发现没有证据表明,对于基线病毒载量高的患者,基于ABC/3TC的方案比基于TDF/FTC的方案导致更多治疗失败。