Division of Neurology, The Children's Hospital of Philadelphia Philadelphia, Pennsylvania ; Department of Neurology, The Perelman School of Medicine at the University of Pennsylvania Philadelphia, Pennsylvania ; Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania Philadelphia, Pennsylvania.
Laboratory for Applied PK/PD, Division of Clinical Pharmacology & Therapeutics, The Children's Hospital of Philadelphia Philadelphia, Pennsylvania.
Ann Clin Transl Neurol. 2014 Nov;1(11):938-52. doi: 10.1002/acn3.131. Epub 2014 Oct 23.
HIV-associated neurocognitive disorder (HAND) is a frequent and heterogeneous complication of HIV, affecting nearly 50% of infected individuals in the combined antiretroviral therapy (cART) era. This is a particularly devastating statistic because the diagnosis of HAND confers an increased risk of HIV-associated morbidity and mortality in affected patients. While cART is helpful in the treatment of the more severe forms of HAND, there is a therapeutic gap in the milder forms of HAND, where cART is less effective. Multiple adjuvant therapies with various mechanisms of action have been studied (N-methyl D-aspartate [NMDA]-receptor antagonists, MAO-B inhibitors, tetracycline-class antibiotics, and others), but none have shown a clear positive effect in HAND. While this lack of efficacy may be because the appropriate therapeutic targets have not yet been determined, we aimed to discuss that study results may also influenced by clinical trial design.
This report is a systematic review of clinical trials of adjuvant therapies for HAND performed from January 1996 through June 2014.
Possible drawbacks in study design, including lack of standardized case definitions, poorly defined target populations, inappropriate dose selection and measurable outcomes, and brief study durations may have masked true underlying mechanistic effects of previously investigated adjuvant therapies for HAND in specific patient populations.
A proposal for streamlining and maximizing the likelihood of success in future clinical studies using a 'learning and confirming' investigational paradigm, incorporating stronger adaptive Phase I/II study designs, computerized modeling, and population/goal of treatment-specific Phase III clinical trials is presented.
艾滋病相关神经认知障碍(HAND)是 HIV 的一种常见且多样的并发症,在联合抗逆转录病毒治疗(cART)时代,近 50%的感染个体受到影响。这是一个特别具有破坏性的统计数据,因为 HAND 的诊断会增加受影响患者与 HIV 相关的发病率和死亡率的风险。虽然 cART 有助于治疗 HAND 的更严重形式,但在 HAND 的较温和形式中存在治疗空白,cART 的效果较差。已经研究了多种具有不同作用机制的辅助治疗方法(N-甲基-D-天冬氨酸 [NMDA] 受体拮抗剂、MAO-B 抑制剂、四环素类抗生素等),但没有一种方法在 HAND 中显示出明显的积极效果。虽然这种疗效不佳可能是因为尚未确定适当的治疗靶点,但我们旨在讨论研究结果也可能受到临床试验设计的影响。
这是一项对 1996 年 1 月至 2014 年 6 月期间进行的 HAND 辅助治疗临床试验的系统评价。
研究设计中可能存在缺陷,包括缺乏标准化的病例定义、目标人群定义不明确、剂量选择和可衡量的结果不当以及研究持续时间短,这可能掩盖了以前针对特定患者群体的 HAND 辅助治疗的潜在机制作用。
提出了一种简化和最大限度提高未来临床试验成功可能性的建议,采用“学习和确认”研究范式,包括更强的适应性 I/II 期研究设计、计算机建模以及针对特定人群/治疗目标的 III 期临床试验。