Treatment outcome for NRTI-sparing regimen consisting of dolutegravir and rilpivirine in HIV-1 infected patients

Mari Kato * , Hiroaki Togami , Atsushi Hirano , Naoko Fukushima , Shuuichi Matsumoto , Yoshiyuki Yokomaku , Masaaki Takahashi
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引用次数: 1

Abstract

Objectives

The nucleoside reverse transcriptase inhibitors (NRTI) have been an important 'back-bone' of an antiretroviral therapy (ART) for HIV-1 infected patients. However, these agents have been associated with both short and long-term toxicity. Therefore, there has been growing interest in evaluating NRTI-sparing regimens. Now we have administered dolutegravir (DTG) and rilpivirine (RPV) to HIV-1 infected patients as a new NRTI-sparing regimen. However, there are few data on the outcome of ART regimen consisting of DTG and RPV. In this study, we examined treatment outcome for this NRTI-sparing regimen in HIV-1 infected patients.

Method

We examined 27 HIV-1 infected patients treated with NRTI-sparing regimen consisting of DTG and RPV in Nagoya Medical Center, Japan. We checked efficacy and safety for this regimen from 2014 to 2015, retrospectively.

Results

Median duration of this NRTI-sparing regimen for 27 Japanese HIV-1 infected patients (26 males, 1 female; mean age 57 years) was 323 days. The reasons for changing to this regimen were pill burden (n=13), lipodystrophy related to NRTI (n=7), myelopathy (n=2), renal dysfunction (n=1), dyslipidemia (n=1), respectively. Finally, 25 patients have continued this regimen. After starting this regimen, HIV viral load were soon less than the detection limit for all patients. Virologic failure and regimen discontinuations by severe adverse reactions were not confirmed for individuals. In addition, abnormal laboratory data (ALT, AST, etc) were not shown for all patients.

Conclusions

Current UK and US treatment guidelines do not recommend NRTI-sparing regimens for people starting ART due to concerns about toxicity, treatment discontinuation, and drug resistance. In this study, 12 patients had been already treated with NRTI-sparing regimen (Raltegravir + RPV). As these patients were elder, it was essential to reduce pill burden. Therefore, a new NRTI-sparing regimen, DTG + RPV, will be available in the future because of reducing pill burden, few drug interactions and low toxicity.

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由多替格拉韦和利匹韦林组成的nrti保留方案在HIV-1感染患者中的治疗结果
目的核苷类逆转录酶抑制剂(NRTI)已成为HIV-1感染患者抗逆转录病毒治疗(ART)的重要“支柱”。然而,这些药物具有短期和长期毒性。因此,人们对评估nrti节约方案越来越感兴趣。现在,我们给HIV-1感染患者使用多替格拉韦(DTG)和利匹韦林(RPV)作为一种新的nrti节约方案。然而,关于由DTG和RPV组成的ART方案的结果的数据很少。在这项研究中,我们检查了这种节省nrti方案在HIV-1感染患者中的治疗结果。方法对日本名古屋医学中心接受DTG + RPV联合nrti保留方案治疗的27例HIV-1感染患者进行分析。我们从2014年到2015年回顾性检查了该方案的有效性和安全性。结果:27名日本HIV-1感染患者(男性26名,女性1名;平均年龄(57岁)为323天。改为该方案的原因分别是药片负担(n=13)、NRTI相关的脂肪营养不良(n=7)、脊髓病(n=2)、肾功能不全(n=1)、血脂异常(n=1)。最后,25名患者继续了这种治疗方案。在开始这种治疗方案后,所有患者的HIV病毒载量很快就低于检测极限。个体的病毒学失败和严重不良反应导致的停药未得到证实。此外,并非所有患者的实验室数据(ALT、AST等)均出现异常。目前英国和美国的治疗指南不建议开始抗逆转录病毒治疗的患者使用nrti -节省方案,因为担心毒性、治疗中断和耐药性。在这项研究中,12例患者已经接受了NRTI-sparing方案(Raltegravir + RPV)的治疗。由于这些患者年龄较大,减轻药物负担至关重要。因此,一种新的节省nrti的方案,DTG + RPV,将在未来可用,因为它减少了药丸负担,药物相互作用少,毒性低。
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