抗逆转录病毒治疗中双重疗法与三重疗法及简化片剂的耐用性和有效性:意大利MOSAICO研究的结果

Durability and effectiveness of dual vs. triple therapy and tablet simplification in ART: findings from the Italian MOSAICO study.

作者信息

Mengato Daniele, Berti Giacomo, Francavilla Andrea, Michielan Silvia, Cappellazzo Linda, Agnoletto Laura, Silvani Maria Chiara, Chiumente Marco, Gregori Dario, Mazzitelli Maria, Venturini Francesca, Cattelan Anna Maria

机构信息

Hospital Pharmacy Unit, Azienda Ospedale-Università Padova, Padova, Italy.

Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac Thoracic Vascular Sciences and Public Health, University of Padova, Padova, Italy.

出版信息

Front Pharmacol. 2025 Aug 6;16:1633968. doi: 10.3389/fphar.2025.1633968. eCollection 2025.

Abstract

INTRODUCTION

Treatment optimization in people with HIV (PWH) has increasingly focused on reducing drug burden and improving regimen simplicity. However, comparative real-world evidence on dual therapy (DT) vs. triple therapy (TT), and single-tablet regimens (STR) vs. multi-tablet regimens (MTR), remains limited.

METHODS

The MOSAICO study is a multicenter, retrospective observational analysis conducted across 20 centers, including people with HIV on a stable virological suppression who switched antiretroviral therapy between 2017 and 2019. People were followed-up up to 48 months post-switch. Comparative analyses assessed virological suppression (HIV-RNA <50 copies/mL), CD4 T cell count, CD4/CD8 ratio, and treatment discontinuation. Propensity score weighting was applied to adjust for baseline differences.

RESULTS

Four hundred ninety-one PWH were included. Both DT and triple therapy groups maintained high levels of virological suppression over 48 months (12 months: 97.1% vs. 91.6%; 24 months: 100% vs. 95.6%; 36 months: 100% vs. 96.9%; 48 months: 100% vs. 100%). From 24 months onward, all persons living with HIV remaining on their respective regimens achieved full virological suppression. Immunological recovery (CD4 count and CD4/CD8 ratio) was comparable across groups, although TT and MTR groups showed greater increases from lower baselines. STRs demonstrated significantly greater treatment durability than MTRs (aHR = 0.56, 95% CI: 0.32-0.97; p = 0.039), while no significant difference in persistence was found between DT and TT. INSTI-based regimens were predominant in DT and MTR arms (DT vs. TT: 84% vs. 46.52%, p < 0.01; MTR vs. STR: 59.38% vs. 47.14%, p < 0.01).

DISCUSSION

The real-world effectiveness of both dual and triple therapies when tailored to appropriate person profiles. STRs offer enhanced long-term persistence compared to MTRs, supporting treatment simplification strategies. These results reinforce the importance of individualized treatment approaches balancing clinical effectiveness with person-centered considerations such as pill burden and tolerability. Limitations include the retrospective design and the lack of quality-of-life data, which may affect interpretation of patient-centered outcomes. Future efforts should expand access to dual-agent STR to further improve Antiretroviral Therapy outcomes.

摘要

引言

艾滋病毒感染者(PWH)的治疗优化越来越注重减轻药物负担和提高治疗方案的简便性。然而,关于双联疗法(DT)与三联疗法(TT)以及单片复方制剂(STR)与多片复方制剂(MTR)的比较真实世界证据仍然有限。

方法

MOSAICO研究是一项多中心回顾性观察分析,在20个中心进行,纳入了2017年至2019年间转换抗逆转录病毒疗法且病毒学抑制稳定的艾滋病毒感染者。在转换治疗后对患者进行长达48个月的随访。比较分析评估了病毒学抑制(HIV-RNA<50拷贝/mL)、CD4 T细胞计数、CD4/CD8比值和治疗中断情况。应用倾向评分加权来调整基线差异。

结果

共纳入491例艾滋病毒感染者。双联疗法组和三联疗法组在48个月内均保持了较高的病毒学抑制水平(12个月:97.1%对91.6%;24个月:100%对95.6%;36个月:100%对96.9%;48个月:100%对100%)。从24个月起,所有继续使用各自治疗方案的艾滋病毒感染者均实现了完全病毒学抑制。各组间免疫恢复(CD4计数和CD4/CD8比值)相当,尽管三联疗法组和多片复方制剂组从较低基线开始的增幅更大。单片复方制剂的治疗持久性显著高于多片复方制剂(aHR = 0.56,95%CI:0.32 - 0.97;p = 0.039),而双联疗法和三联疗法之间在持久性方面未发现显著差异。基于整合酶链转移抑制剂(INSTI)的治疗方案在双联疗法组和多片复方制剂组中占主导地位(双联疗法组与三联疗法组:84%对46.52%,p<0.01;多片复方制剂组与单片复方制剂组:59.38%对47.14%,p<0.01)。

讨论

双联疗法和三联疗法在针对合适患者群体时的真实世界有效性。与多片复方制剂相比,单片复方制剂具有更高的长期持久性,支持治疗简化策略。这些结果强化了个体化治疗方法的重要性,即在临床有效性与以患者为中心的考虑因素(如药片负担和耐受性)之间取得平衡。局限性包括回顾性设计以及缺乏生活质量数据,这可能影响对以患者为中心结局的解释。未来的努力应扩大双联单片复方制剂的可及性,以进一步改善抗逆转录病毒治疗结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d0/12365616/5dab94c25c95/fphar-16-1633968-g001.jpg

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