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优化人类免疫缺陷病毒治疗以改善精准医学的临床结果。

Optimizing Treatment for Human Immunodeficiency Virus to Improve Clinical Outcomes Using Precision Medicine.

出版信息

Am J Epidemiol. 2023 Aug 4;192(8):1341-1349. doi: 10.1093/aje/kwad057.

Abstract

In first-line antiretroviral therapy (ART) for human immunodeficiency virus (HIV) treatment, some subgroups of patients may respond better to an efavirenz-based regimen than an integrase strand transfer inhibitor (InSTI)-based regimen, or vice versa, due to patient characteristics modifying treatment effects. Using data based on nearly 16,000 patients from the North American AIDS Cohort Collaboration on Research and Design from 2009-2016, statistical methods for precision medicine were employed to estimate an optimal treatment rule that minimizes the 5-year risk of the composite outcome of acquired immune deficiency syndrome (AIDS)-defining illnesses, serious non-AIDS events, and all-cause mortality. The treatment rules considered were functions that recommend either an efavirenz- or InSTI-based regimen conditional on baseline patient characteristics such as demographic information, laboratory results, and health history. The estimated 5-year risk under the estimated optimal treatment rule was 10.0% (95% confidence interval (CI): 8.6, 11.3), corresponding to an absolute risk reduction of 2.3% (95% CI: 0.9, 3.8) when compared with recommending an efavirenz-based regimen for all patients and 2.6% (95% CI: 1.0, 4.2) when compared with recommending an InSTI-based regimen for all. Tailoring ART to individual patient characteristics may reduce 5-year risk of the composite outcome compared with assigning all patients the same drug regimen.

摘要

在人类免疫缺陷病毒 (HIV) 治疗的一线抗逆转录病毒治疗 (ART) 中,由于患者特征改变了治疗效果,某些亚组患者可能对基于依非韦伦的方案比基于整合酶链转移抑制剂 (INSTI) 的方案反应更好,或者反之亦然。利用来自 2009-2016 年北美艾滋病队列合作研究与设计的近 16000 名患者的数据,采用精准医学的统计方法来估计一种最佳治疗规则,该规则将最小化获得性免疫缺陷综合征 (AIDS) 定义疾病、严重非 AIDS 事件和全因死亡率复合结局的 5 年风险。所考虑的治疗规则是基于基线患者特征(如人口统计学信息、实验室结果和健康史)的函数,该函数推荐基于依非韦伦或 INSTI 的方案。根据估计的最佳治疗规则,估计的 5 年风险为 10.0%(95%置信区间 [CI]:8.6,11.3),与推荐所有患者使用依非韦伦方案相比,绝对风险降低 2.3%(95% CI:0.9,3.8),与推荐所有患者使用 INSTI 方案相比,绝对风险降低 2.6%(95% CI:1.0,4.2)。根据患者个体特征定制 ART 可能会降低与为所有患者分配相同药物方案相比,复合结局的 5 年风险。

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