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HIV研究网络中接受依曲韦林治疗患者的使用模式及治疗结果

Patterns of Use and Outcomes in Patients Treated with Etravirine in the HIV Research Network.

作者信息

Gebo Kelly, Voss Cindy, Mrus Joseph

机构信息

School of Medicine, Johns Hopkins University, 1830 East Monument Street Suite 435, Baltimore, MD 21287, USA.

出版信息

AIDS Res Treat. 2013;2013:492831. doi: 10.1155/2013/492831. Epub 2013 Jan 29.

DOI:10.1155/2013/492831
PMID:23533731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3603589/
Abstract

This observational analysis examined the clinical outcomes of patients receiving etravirine-(ETR-) based therapy, particularly with protease inhibitors (PIs) other than darunavir (DRV) and with raltegravir (RAL). Data included treatment-experienced adults in the HIV Research Network who began ETR-containing antiretroviral regimens in 2008-2010. The primary objective was to assess 6-month outcomes (durability, i.e., still on an ETR-containing regimen; change in CD4+ cell count and HIV-1 RNA <400 copies/mL). The cohort included 587 patients receiving ETR; 42% of ETR use was in patients not on DRV/ritonavir (r). Patients receiving ETR plus DRV/r had longer durability versus those on ETR plus a PI other than DRV/r at months 6 (91.2% versus 85.5%) and 12 (77.4% versus 65.2%), respectively. Patients on regimens with a PI other than DRV/r were the least likely to be receiving ETR at month 6 (85.5%) versus patients on other ETR-based regimens. Patients on regimens without a PI and without RAL had lower virologic suppression (month 6, 54.2%; month 12, 63.2%) versus patients on other ETR-based regimens. In a clinical care, nontrial setting, ETR was used in regimens without DRV/r. In this population, the 6-month response rates were similar and durable across all regimens, except when ETR was used without RAL and without a PI.

摘要

这项观察性分析研究了接受基于依曲韦林(ETR)治疗的患者的临床结局,特别是与除地瑞那韦(DRV)以外的蛋白酶抑制剂(PIs)以及与拉替拉韦(RAL)联合使用时的情况。数据包括2008 - 2010年在HIV研究网络中开始含ETR抗逆转录病毒治疗方案的有治疗经验的成年人。主要目的是评估6个月的结局(持久性,即仍在接受含ETR的治疗方案;CD4 +细胞计数的变化以及HIV - 1 RNA<400拷贝/mL)。该队列包括587例接受ETR治疗的患者;42%的ETR使用情况是在未接受DRV/利托那韦(r)的患者中。接受ETR加DRV/r的患者在第6个月(91.2%对85.5%)和第12个月(77.4%对65.2%)的持久性分别长于接受ETR加除DRV/r以外的PI的患者。在第6个月时,接受除DRV/r以外的PI治疗方案的患者接受ETR治疗的可能性最小(85.5%),与接受其他基于ETR的治疗方案的患者相比。与接受其他基于ETR的治疗方案的患者相比,未使用PI且未使用RAL的治疗方案的患者病毒学抑制率较低(第6个月为54.2%;第12个月为63.2%)。在临床护理的非试验环境中,ETR用于不含DRV/r的治疗方案。在该人群中,除了未使用RAL且未使用PI而使用ETR的情况外,所有治疗方案的6个月反应率相似且持久。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fccc/3603589/059e5f84ebd5/ART2013-492831.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fccc/3603589/059e5f84ebd5/ART2013-492831.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fccc/3603589/059e5f84ebd5/ART2013-492831.001.jpg

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本文引用的文献

1
Similar efficacy of raltegravir when used with or without a protease inhibitor in treatment-experienced patients.在经治患者中,无论是否联用蛋白酶抑制剂,雷特格韦疗效相似。
HIV Clin Trials. 2011 May-Jun;12(3):131-40. doi: 10.1310/hct1203-131.
2
Raltegravir, maraviroc, etravirine: an effective protease inhibitor and nucleoside reverse transcriptase inhibitor-sparing regimen for salvage therapy in HIV-infected patients with triple-class experience.拉替拉韦、马拉维若、依曲韦林:一种有效的蛋白酶抑制剂和核苷逆转录酶抑制剂节省方案,用于治疗有三重耐药经验的 HIV 感染患者的挽救治疗。
AIDS. 2010 Mar 27;24(6):924-8. doi: 10.1097/QAD.0b013e3283372d76.
3
Efficacy, safety, and tolerability of etravirine with and without darunavir/ritonavir or raltegravir in treatment-experienced patients: analysis of the etravirine early access program in the United States.
依曲韦林在有或无达芦那韦/利托那韦或雷特格韦治疗经治患者中的疗效、安全性和耐受性:美国依曲韦林早期准入计划分析。
J Acquir Immune Defic Syndr. 2010 Apr;53(5):614-8. doi: 10.1097/QAI.0b013e3181cdebb1.
4
Efficacy and safety of etravirine in treatment-experienced, HIV-1 patients: pooled 48 week analysis of two randomized, controlled trials.依发韦仑治疗经治 HIV-1 患者的疗效和安全性:两项随机对照试验的 48 周汇总分析。
AIDS. 2009 Nov 13;23(17):2289-300. doi: 10.1097/QAD.0b013e3283316a5e.