Siegel Scott D, Budziszewski Ross, Layton Essie, Nam Brian, Schnoll Robert
Helen F. Graham Cancer Center & Research Institute, ChristianaCare, United States.
Department of Psychiatry and Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, United States.
Drug Alcohol Depend Rep. 2024 Aug 17;12:100275. doi: 10.1016/j.dadr.2024.100275. eCollection 2024 Sep.
Patients with pulmonary nodules detected through lung cancer screening or as incidental findings are often followed in lung health and screening programs. The use of personalized pharmacotherapy for smoking cessation informed by the nicotine metabolite ratio (NMR), a measure of nicotine metabolism, has not yet been evaluated in this setting. This pilot randomized controlled trial (RCT) evaluated the feasibility of conducting a larger trial.
Through a pragmatic RCT design, participants were recruited from a Mid-Atlantic lung health and screening program. Eligible participants smoked >5 cigarettes per day and completed a blood draw to determine NMR before being randomized to standard or NMR-guided care treatment arms. Standard care participants were offered nicotine replacement therapy (NRT) or varenicline and a referral to phone-based smoking cessation counseling. NMR-guided participants received standard care except they were provided a personalized medication recommendation based on their NMR. Study outcomes included measures of feasibility, medication uptake, and treatment matching (i.e., uptake of the optimal medication).
More than 80 % of 205 screened patients were eligible. However, only 37 (22 %) of these patients enrolled in the study, with a mean age of 65 years, 43 % female, and 25 % Black. Nearly all patients who declined cited a disinterest in smoking cessation. Participants in both treatment arms had high rates of medication uptake (68 %), with NMR-guided participants showing a trend towards greater treatment matching (55 % vs. 29 %).
The results of this pilot study provide support for conducting a larger RCT of an NMR-guided smoking cessation intervention in a lung health and screening setting. Consideration should be given to augmenting the intervention to address barriers to study entry.
通过肺癌筛查或偶然发现的肺结节患者通常在肺部健康和筛查项目中接受随访。基于尼古丁代谢产物比率(NMR,一种尼古丁代谢的指标)进行个性化戒烟药物治疗在这种情况下尚未得到评估。这项试点随机对照试验(RCT)评估了开展更大规模试验的可行性。
通过务实的RCT设计,从大西洋中部的肺部健康和筛查项目中招募参与者。符合条件的参与者每天吸烟超过5支,在随机分配到标准治疗组或NMR指导治疗组之前完成血液检测以确定NMR。标准治疗组的参与者可获得尼古丁替代疗法(NRT)或伐尼克兰,并被转介接受电话戒烟咨询。NMR指导组的参与者接受标准治疗,但根据其NMR获得个性化药物推荐。研究结果包括可行性、药物使用情况和治疗匹配度(即最佳药物的使用情况)的测量。
205名筛查患者中超过80%符合条件。然而,这些患者中只有37名(22%)参加了研究,平均年龄为65岁,43%为女性,25%为黑人。几乎所有拒绝的患者都表示对戒烟不感兴趣。两个治疗组的参与者药物使用率都很高(68%),NMR指导组的参与者在治疗匹配度上有更高的趋势(55%对29%)。
这项试点研究的结果为在肺部健康和筛查环境中开展更大规模的NMR指导戒烟干预随机对照试验提供了支持。应考虑加强干预措施以解决研究入组的障碍。