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接受临床护理的HIV感染者中二线抗逆转录病毒联合治疗方案的疗效:一项多中心队列研究

Outcomes of second combination antiretroviral therapy regimens among HIV-infected persons in clinical care: a multicenter cohort study.

作者信息

Napravnik Sonia, Eron Joseph J, Sterling Timothy R, Juday Timothy, Uy Jonathan, Moore Richard D

机构信息

Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7215, USA.

出版信息

AIDS Res Hum Retroviruses. 2013 Mar;29(3):574-80. doi: 10.1089/AID.2012.0210. Epub 2012 Nov 12.

Abstract

Data on the effectiveness of second-line combination antiretroviral therapy (cART) are limited. We evaluated virologic outcomes of second cART in a multicenter cohort collaboration. The study population initiated first and second modern cART between 1996 and 2010. The second cART required a switch in at least the anchor agent of first cART. We evaluated time to virologic failure of second cART and factors associated with greater risk of failure using multivariable Cox proportional hazards models. Of 488 patients who switched to second-line cART, 67% were black and 32% were women. The median HIV-1 RNA at second cART initiation was 9,565 copies/ml [interquartile range (IQR); 123, 94,108]. The time to virologic failure of second cART was longer if HIV-1 RNA was undetectable at switch (p=0.001), although 12% and 17% of patients with undetectable and detectable HIV-1 RNA experienced virologic failure within 6 months of second cART initiation, respectively. A lower CD4 cell count at second cART initiation was associated with a greater risk of virologic failure. Failure rates decreased in more recent calendar years [adjusted relative hazard of 0.40 comparing 2008 to 2010 with 1996 to 1998 (95% confidence interval; 0.15, 1.00)]; however, type of anchor agent was not associated with failure. In conclusion, virologic failure of second cART was less likely if patients switched with undetectable HIV-1 RNA, although risk of early failure was similar. The effectiveness of second cART regimens improved over calendar time and was independent of the anchor agent in the regimen.

摘要

二线联合抗逆转录病毒疗法(cART)有效性的数据有限。我们在一项多中心队列合作研究中评估了二线cART的病毒学转归。研究人群在1996年至2010年间开始接受一线和二线现代cART治疗。二线cART至少需要更换一线cART的主要药物。我们使用多变量Cox比例风险模型评估了二线cART的病毒学失败时间以及与更高失败风险相关的因素。在488例转换为二线cART的患者中,67%为黑人,32%为女性。二线cART开始时HIV-1 RNA的中位数为9565拷贝/毫升[四分位间距(IQR);123,94108]。如果转换时HIV-1 RNA不可检测,二线cART的病毒学失败时间会更长(p=0.001),尽管在二线cART开始后6个月内,HIV-1 RNA不可检测和可检测的患者分别有12%和17%发生了病毒学失败。二线cART开始时较低的CD4细胞计数与更高的病毒学失败风险相关。在最近几年中失败率有所下降[比较2008年至2010年与1996年至1998年,调整后的相对风险为0.40(95%置信区间;0.15,1.00)];然而,主要药物的类型与失败无关。总之,如果患者在HIV-1 RNA不可检测时转换治疗,二线cART的病毒学失败可能性较小,尽管早期失败风险相似。二线cART方案的有效性随时间推移有所改善,且与方案中的主要药物无关。

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