Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Lancet HIV. 2019 Jul;6(7):e475-e482. doi: 10.1016/S2352-3018(19)30133-X. Epub 2019 May 8.
Despite the recent success of antiretrovirals for HIV prevention, additional, more effective, or more acceptable biomedical interventions will ultimately be needed to end the HIV epidemic. Designing clinical trials to evaluate the efficacy of new products that reduce HIV infection risk is challenging because of the existence of highly effective interventions to prevent HIV. However, the implementation of these interventions is uneven, and the fact that multiple HIV prevention efficacy trials are currently evaluating new products means the field confronts uncertainty in the emerging standard of prevention. In this Viewpoint, we take stock of the current state of HIV prevention, and subsequently discuss the key challenges in designing future trials to evaluate the next generation of HIV prevention products. We also highlight gaps in the knowledge base that need to be addressed to advance the design of research. Future trials are tenable, even in the context of existing and effective interventions, and should involve careful statistical approaches and multidisciplinary collaborative design.
尽管最近抗逆转录病毒药物在预防 HIV 方面取得了成功,但最终仍需要更多有效、更能被接受的生物医学干预措施来终结 HIV 流行。由于存在预防 HIV 的高效干预措施,设计临床试验来评估降低 HIV 感染风险的新产品的疗效具有挑战性。然而,这些干预措施的实施并不均衡,而且目前有多项 HIV 预防功效试验正在评估新产品,这意味着该领域面临新兴预防标准的不确定性。在本观点文章中,我们对当前的 HIV 预防状况进行了评估,随后讨论了设计未来试验以评估下一代 HIV 预防产品所面临的关键挑战。我们还强调了需要解决的知识库中的差距,以推进研究设计。即使在现有和有效的干预措施的背景下,未来的试验也是可行的,并且应该涉及仔细的统计方法和多学科协作设计。