Andreatta Kristen, Sax Paul E, Wohl David, D'Antoni Michelle L, Liu Hui, Hindman Jason T, Callebaut Christian
Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
Division of Infectious Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
J Antimicrob Chemother. 2025 Jan 3;80(1):281-291. doi: 10.1093/jac/dkae407.
Five Phase 3 bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) clinical studies demonstrated that the efficacy of B/F/TAF was non-inferior to dolutegravir (DTG) + 2 NRTIs. We retrospectively assessed drug adherence and effect on virologic outcomes.
Studies (NCT02607930, NCT02607956, NCT03547908, NCT02603120 and NCT03110380) were double-blind, placebo-controlled and enrolled treatment-naïve or virologically suppressed adults. Adherence was calculated by pill count from returned pill bottles; virologic outcome was assessed by last on-treatment HIV-1 RNA.
Altogether, 2622 participants (B/F/TAF: n = 1306; DTG + 2 NRTIs: n = 1316) were categorized as having high (≥95%), intermediate (≥85% to <95%) or low (<85%) adherence. Through Week 48, low adherence was observed in 46 (3.5%) participants in the B/F/TAF group (78% median adherence) and 69 (5.2%) in the DTG + 2 NRTI group (80% median adherence). Overall, 1287 (98.5%) participants in the B/F/TAF group and 1292 (98.2%) in the DTG + 2 NRTI group had virologic suppression (VS; HIV-1 RNA < 50 copies/mL) through Week 48. VS in participants with low adherence versus high or intermediate adherence was similar in the B/F/TAF group, but lower in the DTG + 2 NRTI group (P ≤ 0.002). Similar results were observed at Weeks 96 and 144. Two participants (<95% adherence) in the DTG + 2 NRTI group receiving DTG and abacavir/lamivudine developed M184V; there was no treatment-emergent resistance to B/F/TAF.
Participants with suboptimal (<85%) adherence to B/F/TAF maintained high levels of VS, whereas suboptimal DTG + 2 NRTI adherence was associated with lower VS.
五项3期比克替拉韦/恩曲他滨/替诺福韦艾拉酚胺(B/F/TAF)临床研究表明,B/F/TAF的疗效不劣于度鲁特韦(DTG)+两种核苷类逆转录酶抑制剂(NRTIs)。我们进行了回顾性评估,以分析药物依从性及其对病毒学结果的影响。
研究(NCT02607930、NCT02607956、NCT03547908、NCT02603120和NCT03110380)为双盲、安慰剂对照试验,纳入初治或病毒学抑制的成年人。通过回收药瓶中的药丸计数计算依从性;通过最后一次治疗时的HIV-1 RNA评估病毒学结果。
总共2622名参与者(B/F/TAF组:n = 1306;DTG + 两种NRTIs组:n = 1316)被分类为依从性高(≥95%)、中等(≥85%至<95%)或低(<85%)。到第48周时,B/F/TAF组有46名(3.5%)参与者依从性低(依从性中位数为78%),DTG + 两种NRTIs组有69名(5.2%)参与者依从性低(依从性中位数为80%)。总体而言,到第48周时,B/F/TAF组1287名(98.5%)参与者和DTG + 两种NRTIs组1292名(98.2%)参与者实现了病毒学抑制(VS;HIV-1 RNA < 50拷贝/mL)。B/F/TAF组中依从性低的参与者与依从性高或中等的参与者相比,VS情况相似,但DTG + 两种NRTIs组中依从性低的参与者VS情况较低(P≤0.002)。在第96周和第144周时观察到类似结果。接受DTG和阿巴卡韦/拉米夫定的DTG + 两种NRTIs组中有两名参与者(依从性<95%)出现了M184V;B/F/TAF未出现新的治疗引发的耐药性。
B/F/TAF依从性欠佳(<85%)的参与者仍保持较高水平的VS,而DTG + 两种NRTIs依从性欠佳则与较低的VS相关。