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Antiretroviral salvage therapy for multiclass drug-resistant HIV-1-infected patients: from clinical trials to daily clinical practice.

机译:抗逆转录病毒挽救疗法,用于多类耐药HIV-1感染患者:从临床试验到日常临床实践。

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摘要

Drug resistance is one of the key problems in the management of long-term HIV-1-infected patients. Due to cross-resistance patterns within classes, broad resistance to the three original antiretroviral classes can develop in some patients, mainly those with extensive antiretroviral treatment experience and multiple treatment failures. Triple-class-resistant HIV-1 infection has been associated with a higher risk of clinical progression and death. Additionally, it increases the probability of transmission of multidrug-resistant HIV-1 strains. Over the last years, the availability of new antiretroviral agents against novel targets (integrase inhibitors and CCR5 antagonists), and new drugs within old classes (nonnucleoside reverse transcriptase inhibitors and protease inhibitors) has opened a range of new therapeutic options for patients with multiclass drug-resistant HIV-1 infection and scarce therapeutic options with previous drugs. In randomized clinical trials, each of these new drugs has shown exceptional efficacy results, especially in patients who received other fully active drugs in the regimen. Indeed, in nonrandomized trials and observational studies, unprecedented rates of virologic suppression similar to those obtained in naive patients have been achieved when three of the currently available new drugs were combined, even in heavily experienced patients who had no viable salvage options with the previous classes. Thus, the goal of suppression and maintenance (plasma HIV-1 RNA < 50 copies/ml) is now also attainable in patients with multidrug-resistant HIV-1 infection. Treatment failure can still occur, however, and the management of patients with multidrug-resistant HIV-1 infection remains a challenge. Clinicians are encouraged to optimize use of the new drugs to obtain better control of HIV infection while avoiding emergence of new resistance-associated mutations. The aim of this article is to summarize current knowledge on the management of salvage therapy for patients with multidrug-resistant HIV-1 infection by analyzing the evidence extracted from clinical trials, and to review the information on the effectiveness of triple combinations of new drugs provided by non-comparative trials and observational studies.
机译:耐药性是治疗长期感染HIV-1的患者的关键问题之一。由于类别内的交叉耐药模式,某些患者可能会产生对三种原始抗逆转录病毒类别的广泛耐药性,主要是那些具有丰富的抗逆转录病毒治疗经验和多次治疗失败的患者。具有三重抗药性的HIV-1感染与临床进展和死亡的较高风险相关。此外,它增加了耐多药HIV-1菌株的传播可能性。在过去的几年中,针对新型靶标的新抗逆转录病毒药物(整合酶抑制剂和CCR5拮抗剂)以及旧类别中的新药物(非核苷逆转录酶抑制剂和蛋白酶抑制剂)的推出为多种药物的患者打开了一系列新的治疗选择耐药的HIV-1感染,以前的药物缺乏治疗选择。在随机临床试验中,这些新药均显示出优异的疗效,尤其是在该方案中接受其他全活性药物的患者中。的确,在非随机试验和观察性研究中,当将三种当前可用的新药合用时,即使在经验丰富的患者中,如前者没有可行的挽救选择,即使是经验丰富的患者,其病毒学抑制率也达到了与未治疗患者相似的前所未有的病毒学抑制率。因此,在具有多重耐药性的HIV-1感染患者中,也可以实现抑制和维持(血浆HIV-1 RNA <50拷贝/ ml)的目标。然而,治疗失败仍然可能发生,对具有多重耐药性的HIV-1感染的患者的管理仍然是一个挑战。鼓励临床医生优化使用新药,以更好地控制HIV感染,同时避免出现新的耐药相关突变。本文的目的是通过分析从临床试验中提取的证据,总结目前对具有多重耐药性HIV-1感染的患者进行挽救疗法管理的知识,并复习所提供的三联新药有效性的信息。通过非对比试验和观察性研究。

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