Siegel Scott D, Tindle Hilary A, Bergen Andrew W, Tyndale Rachel F, Schnoll Robert
Christiana Care Health System, Helen F. Graham Cancer Center & Research Institute and Institute for Research on Equity & Community Health, 4701, gletown-Stanton Road, Newark, DE 19713, United States.
Department of Medicine and Vanderbilt Ingram Cancer Center, Vanderbilt University, United States.
Addict Neurosci. 2023 Jun;6. doi: 10.1016/j.addicn.2023.100076. Epub 2023 Feb 16.
This review summarizes the evidence to date on the development of biomarkers for personalizing the pharmacological treatment of combustible tobacco use. First, the latest evidence on FDA-approved medications is considered, demonstrating that, while these medications offer real benefits, they do not contribute to smoking cessation in approximately two-thirds of cases. Second, the case for using biomarkers to guide tobacco treatment is made based on the potential to increase medication effectiveness and uptake and reduce side effects. Next, the FDA framework of biomarker development is presented along with the state of science on biomarkers for tobacco treatment, including a review of the nicotine metabolite ratio, electroencephalographic event-related potentials, and other biomarkers utilized for risk feedback. We conclude with a discussion of the challenges and opportunities for the translation of biomarkers to guide tobacco treatment and propose priorities for future research.
本综述总结了迄今为止关于开发用于个性化可燃烟草使用药物治疗的生物标志物的证据。首先,考虑了美国食品药品监督管理局(FDA)批准药物的最新证据,表明虽然这些药物确实带来了实际益处,但在大约三分之二的病例中并不能促进戒烟。其次,基于提高药物有效性和使用率以及减少副作用的潜力,提出了使用生物标志物指导烟草治疗的理由。接下来,介绍了FDA生物标志物开发框架以及烟草治疗生物标志物的科学现状,包括对尼古丁代谢物比率、脑电图事件相关电位以及用于风险反馈的其他生物标志物的综述。我们最后讨论了将生物标志物转化以指导烟草治疗所面临的挑战和机遇,并提出了未来研究的重点。