Saag Michael S, Westfall Andrew O, Cole Stephen R, Mathews William C, Drozd Daniel R, Mayer Kenneth H, Burkholder Greer A, Kitahata Mari, Maiese Eric M
*Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL; †Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL; ‡Department of Epidemiology, University of North Carolina, Chapel Hill, NC; §Owen Clinic, University of California, San Diego, San Diego, CA; ‖Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA; ¶Fenway Health Clinic, Boston, MA; #Department of Medicine, Harvard Medical School, Boston, MA; and **Merck Sharp & Dohme Corp., Kenilworth, NJ.
J Acquir Immune Defic Syndr. 2017 Jan 1;74(1):60-64. doi: 10.1097/QAI.0000000000001168.
We examined factors associated with selection of initial antiretroviral regimen in the CNICS cohort. Patients initiating antiretroviral therapy between July 2009 and December 2012 were classified as receiving a nonnucleoside reverse transcriptase inhibitor (NNRTI)-, boosted protease inhibitor (PI)-, or raltegravir-based regimen. Among 873 patients initiating antiretroviral therapy, 488 regimens contained an NNRTI, 319 a boosted PI, and 66 raltegravir. Patients with depression and women were less likely to receive an NNRTI, whereas those with underlying cardiovascular disease, liver disease, and those coinfected with hepatitis C were more likely to receive raltegravir. Those with baseline viral load >100,000 c/ml and those with substance use were more likely to receive a boosted PI. Thus, in the "real world," ARV regimen choices appear to take into account adverse effects and patient baseline characteristics. Factors that impact initial regimen selection will likely become more heterogeneous over time as more choices for HIV therapy become available.
我们在CNICS队列中研究了与初始抗逆转录病毒治疗方案选择相关的因素。2009年7月至2012年12月开始接受抗逆转录病毒治疗的患者被分类为接受基于非核苷类逆转录酶抑制剂(NNRTI)、增强型蛋白酶抑制剂(PI)或拉替拉韦的治疗方案。在873例开始接受抗逆转录病毒治疗的患者中,488个方案包含NNRTI,319个包含增强型PI,66个包含拉替拉韦。患有抑郁症的患者和女性接受NNRTI的可能性较小,而患有潜在心血管疾病、肝病以及合并丙型肝炎感染的患者更有可能接受拉替拉韦。基线病毒载量>100,000拷贝/毫升的患者和有药物使用史的患者更有可能接受增强型PI。因此,在“现实世界”中,抗逆转录病毒治疗方案的选择似乎会考虑不良反应和患者的基线特征。随着可用于HIV治疗的选择越来越多,影响初始治疗方案选择的因素可能会随着时间的推移变得更加多样化。