Jubb Becky, Lewis Marilyn, McFadyen Lynn, Simpson Paul, Mori Julie, Chan Phylinda, Weatherley Barry, van der Ryst Elna, Westby Mike, Craig Charles
Pfizer Inc, Clinical Group, Rare Disease, Groton, CT, USA.
The Research Network, Sandwich, UK.
Antivir Chem Chemother. 2019 Jan-Dec;27:2040206619895706. doi: 10.1177/2040206619895706.
Maraviroc blocks HIV-1 entry into CD4+ cells by interrupting the interaction between viral gp120 and cell-surface CCR5. Resistance to CCR5 antagonist–mediated inhibition can develop by unmasking pre-existing CXCR4-using virus or through selection of CCR5-tropic resistant virus, characterized by plateaus in maximum percent inhibition <95%. Here, we examine viral escape in maraviroc-treated participants during virologic failure through Week 48 in the MOTIVATE 1 and 2 trials. Resistance was assessed relative to number of active drugs in participants’ optimized background therapy, pharmacokinetic adherence markers, Baseline demographic data, HIV-1 RNA and CD4+ counts. For participants with R5 virus confirmed () at Screening, Baseline genotypic weighted optimized background therapy susceptibility scores (gwOBTSS) were assigned where possible. Through Week 48, 219/392 (56%) participants with an assigned gwOBTSS achieved a virologic response. Of those remaining, 48/392 (12%) had CXCR4-using virus; 58/392 (15%) had R5 virus (maraviroc sensitive: = 35/392, 9%; maraviroc resistant: = 18/392, 5%; undeterminable: = 5/392, 1%) and 67/392 (17%) had no failure tropism result. When optimized background therapy provided limited support to maraviroc (gwOBTSS <2), 143/286 (50%) responded to therapy, while 76/106 (72%) participants with gwOBTSS ≥2 responded ( < 0.001). Resistance rates were highest for participants with gwOBTSS <2, accounting for 45/48 (94%) of total CXCR4-using emergence and 18/18 (100%) of total CCR5-tropic resistance. R5 viruses from participants with gwOBTSS ≥2 ( = 10) were exclusively maraviroc sensitive; five of these participants had pharmacokinetic and/or pill-count markers of non-adherence. When co-administered with a fully active background regimen, maraviroc did not readily generate resistance in the clinical setting.
: ClinicalTrials.gov (https://clinicaltrials.gov/), NCT00098722 and NCT00098306
马拉维若通过阻断病毒糖蛋白120与细胞表面趋化因子受体5(CCR5)之间的相互作用,阻止HIV-1进入CD4+细胞。对CCR5拮抗剂介导的抑制作用产生耐药性的情况,可通过使预先存在的利用CXCR4的病毒暴露或通过选择对CCR5具有嗜性的耐药病毒而出现,其特征为最大抑制百分比出现平台期且<95%。在此,我们在MOTIVATE 1和2试验中,研究了在病毒学失败期间接受马拉维若治疗的参与者直至第48周时的病毒逃逸情况。根据参与者优化背景治疗中的活性药物数量、药代动力学依从性指标、基线人口统计学数据、HIV-1 RNA和CD4+细胞计数来评估耐药性。对于在筛查时确诊为R5病毒()的参与者,尽可能分配基线基因型加权优化背景治疗敏感性评分(gwOBTSS)。直至第48周,219/392(56%)名分配了gwOBTSS的参与者实现了病毒学应答。在其余参与者中,48/392(12%)具有利用CXCR4的病毒;58/392(15%)具有R5病毒(对马拉维若敏感: = 35/392,9%;对马拉维若耐药: = 18/392,5%;无法确定: = 5/392,1%),67/392(17%)没有失败嗜性结果。当优化背景治疗对马拉维若的支持有限(gwOBTSS <2)时,143/286(50%)的参与者对治疗有反应,而gwOBTSS≥2的76/106(72%)名参与者有反应(<0.001)。gwOBTSS <2的参与者耐药率最高,占利用CXCR4的病毒出现总数中的45/48(94%)以及对CCR5具有嗜性的耐药总数中的18/18(100%)。gwOBTSS≥2的参与者( = 10)的R5病毒均对马拉维若敏感;其中五名参与者有药代动力学和/或服药计数的不依从指标。当与完全有效的背景治疗方案联合使用时,马拉维若在临床环境中不易产生耐药性。
ClinicalTrials.gov(https://clinicaltrials.gov/),NCT00098722和NCT00098306