Hospital Clínic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
J Antimicrob Chemother. 2018 Jul 1;73(7):1965-1971. doi: 10.1093/jac/dky093.
No controlled comparisons between dolutegravir/lamivudine or dolutegravir maintenance therapy have been done. We hypothesized that these options would have similar efficacy to triple ART.
We used an open-label non-inferiority randomized controlled trial comprising two phases: phase A was established to test that experimental arms did not have an unacceptable (≥5%) failure rate; phase B was intended to include the full number of patients followed for 48 weeks. Treated HIV-1-infected adults with viral load <50 copies/mL for ≥12 months, no prior viral failure or resistance mutations to study drugs, nadir CD4 >200 cells/mm3, and hepatitis B virus surface antigen negative were randomized 1:1:1 to maintain triple therapy (control arm), or to switch to dolutegravir/lamivudine, or to dolutegravir monotherapy stratifying by anchor drug. Premature discontinuation was considered if viral failure or therapy interruption due to adverse events, concurrent illness, protocol deviation or patient's wish occurred. Blips were registered. Planned phase A results at 24 weeks are reported here. The study is registered at EudraCT: 201500027435.
Ninety-one (control, n = 31; dual therapy, n = 29; monotherapy, n = 31) patients were randomized. Three patients (none previously exposed to integrase inhibitors) prematurely discontinued treatment due to viral failure: dolutegravir/lamivudine (n = 1), no resistance mutations (subject A); dolutegravir (n = 2), N155H, S147G and Q148R resistance mutations (subject B), and E138K, G140S and N155H resistance mutations (subject C). There were no discontinuations for other reasons. One patient (dolutegravir/lamivudine) experienced a blip in viral load. The Data Safety Monitoring Board recommended stopping the dolutegravir monotherapy arm.
In contrast to dolutegravir/lamivudine, a higher than expected risk of viral failure with development of cross-resistance integrase mutations occurred with dolutegravir maintenance monotherapy.
尚未对多替拉韦/拉米夫定或多替拉韦维持治疗进行对照研究。我们假设这些选择与三联抗逆转录病毒治疗(ART)的疗效相似。
我们采用了一项开放标签的非劣效性随机对照临床试验,包括两个阶段:A 阶段旨在测试实验臂不会出现不可接受的(≥5%)失败率;B 阶段旨在纳入随访 48 周的全部患者。治疗前 HIV-1 感染患者的病毒载量<50 拷贝/ml 至少 12 个月,无先前的病毒失败或对研究药物的耐药突变,最低 CD4 细胞计数>200 个/mm3,乙型肝炎病毒表面抗原阴性,按 1:1:1 比例随机分为维持三联治疗(对照组)、转换为多替拉韦/拉米夫定或多替拉韦单药治疗,按锚定药物分层。如果出现病毒失败或因不良反应、合并疾病、方案偏离或患者意愿而中断治疗,则提前停药。记录病毒学突破。这里报告计划的 A 阶段 24 周结果。该研究在 EudraCT 注册:201500027435。
91 名(对照组 n=31;双药治疗组 n=29;单药治疗组 n=31)患者被随机分组。3 名患者(均无整合酶抑制剂暴露史)因病毒失败提前停药:多替拉韦/拉米夫定组(n=1),无耐药突变(患者 A);多替拉韦组(n=2),N155H、S147G 和 Q148R 耐药突变(患者 B)和 E138K、G140S 和 N155H 耐药突变(患者 C)。无其他原因停药。1 名患者(多替拉韦/拉米夫定)发生病毒载量突破。数据安全监测委员会建议停止多替拉韦单药治疗组。
与多替拉韦/拉米夫定相比,多替拉韦维持单药治疗出现交叉耐药整合酶突变导致病毒失败的风险高于预期。