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Switching regimens in virologically suppressed HIV-1-infected patients: evidence base and rationale for integrase strand transfer inhibitor (INSTI)-containing regimens

机译:病毒学抑制的HIV-1感染患者的转换方案:包含整合酶链转移抑制剂(INSTI)方案的证据基础和原理

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In an era when most individuals with treated HIV infection can expect to live into old age, clinicians should proactively review their patients' current and future treatment needs and challenges. Clinical guidelines acknowledge that, in the setting of virological suppression, treatment switch may yield benefits in terms of tolerability, regimen simplification, adherence, convenience and long-term health considerations, particularly in the context of ageing. In this paper, we review evidence from six key clinical studies on switching virologically suppressed patients to regimens based on integrase strand transfer inhibitors (INSTIs), the antiretroviral class increasingly preferred as initial therapy in clinical guidelines. We review these studies and focus on the virological efficacy, safety, and tolerability of switching to INSTI-based regimens in suppressed HIV-positive individuals. We review the early switch studies SWITCHMRK and SPIRAL [assessing a switch from a ritonavir-boosted protease inhibitor (PI/r) to raltegravir (RAL)-containing regimens], together with data from STRATEGY-PI [assessing a switch to elvitegravir (EVG)-containing regimens; EVG/cobicistat (COBI)/emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF) vs. remaining on a PI/r-containing regimen], STRATEGY-NNRTI [assessing a switch to EVG/COBI/FTC/TDF vs. continuation of a nonnucleoside reverse transcriptase inhibitor (NNRTI) and two nucleoside reverse transcriptase inhibitors (NRTIs)], STRIIVING [assessing a switch to a dolutegravir (DTG)-containing regimen (abacavir (ABC)/lamivudine (3TC)/DTG) vs. staying on the background regimen], and GS study 109 [assessing a switch to EVG/COBI/FTC/tenofovir alafenamide fumarate (TAF) vs. continuation of FTC/TDF-based regimens]. Switching to INSTI-containing regimens has been shown to support good virological efficacy, with evidence from two studies demonstrating superior virological efficacy for a switch to EVG-containing regimens. In addition, switching to INSTI regimens was associated with improved tolerability and greater reported patient satisfaction and outcomes in some studies. INSTI-based regimens offer an important contemporary switch option that may be tailored to meet and optimize the needs of many patients.
机译:在一个大多数接受HIV感染治疗的人都有望长寿的时代,临床医生应积极回顾患者当前和将来的治疗需求和挑战。临床指南承认,在病毒抑制的情况下,治疗的转换可能会在耐受性,简化方案,依从性,便利性和长期健康考虑方面产生益处,尤其是在衰老的情况下。在本文中,我们回顾了六项关键临床研究的证据,这些研究基于整体整合链转移抑制剂(INSTI)将病毒学抑制的患者改用方案,抗逆转录病毒药物在临床指南中日益被选作初始治疗。我们回顾了这些研究,并着重于在HIV阳性个体中转用基于INSTI的治疗方案的病毒学功效,安全性和耐受性。我们回顾了早期的转换研究SWITCHMRK和SPIRAL [评估从利托那韦增强蛋白酶抑制剂(PI / r)转换为含raltegravir(RAL)的治疗方案],以及来自STRATEGY-PI的数据[评估转换为elvitegravir(EVG) )含方案; EVG / cobicistat(COBI)/ emtricitabine(FTC)/替诺福韦富马酸替诺福韦(TDF)与仍然采用含PI / r的方案],STRATEGY-NNRTI [评估向EVG / COBI / FTC / TDF的转换与继续使用一个非核苷类逆转录酶抑制剂(NNRTI)和两个核苷类逆转录酶抑制剂(NRTIs),STRIFIVING [评估是否改用含dolutegravir(DTG)的治疗方案(阿巴卡韦(ABC)/拉米夫定(3TC)/ DTG), GS] [背景方案]和GS研究109 [评估转用EVG / COBI / FTC /替诺福韦阿拉法酰胺富马酸盐(TAF)与基于FTC / TDF方案的延续]。业已证明,转向含INSTI的方案具有良好的病毒学疗效,两项研究表明,向含EVG方案的转化具有更高的病毒学功效。此外,在某些研究中,改用INSTI方案可改善耐受性,并提高患者的满意度和预后。基于INSTI的治疗方案提供了一种重要的当代转换方案,可以根据需要量身定制,以满足并优化许多患者的需求。

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