Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland; Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, New York.
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
J Thorac Oncol. 2017 Nov;12(11):1646-1653. doi: 10.1016/j.jtho.2017.08.001. Epub 2017 Aug 14.
Selecting individuals on the basis of model-predicted risks has been reported to improve lung cancer screening efficiency. On the basis of case-control studies, time to first cigarette (TTFC), a nicotine dependency measurement, has been a strong independent predictor of lung cancer risk. Our objective was to verify the TTFC-lung cancer association in the prospective National Lung Screening Trial and evaluate whether adding TTFC can improve lung cancer risk-prediction models.
Using Cox models, we examined associations between TTFC (≤5, 6-14, 15-29, 30-59, and ≥60 minutes) and lung cancer incidence and death in 18,729 National Lung Screening Trial participants, adjusting for smoking and other lung cancer risk factors comprehensively. We estimated 5-year individual lung cancer incidence by using models without and with TTFC and dichotomized into screening or no-screening groups based on risk thresholds of 1% and 2%. Area under the receiver operating curve values were calculated for models without and with TTFC.
Smokers with a TTFC of 60 minutes or more had a much lower standardized 5-year lung cancer incidence risk-1.54% (1.52%-1.56%) for TTFC 60 minutes or more versus 4.07% (4.04%-4.09%) for TTFC 5 minutes or less-and lung cancer death risk-0.59% (0.57%-0.61%) for TTFC 60 minutes or more versus 2.26% (2.23%-2.28%) for TTFC 5 minutes or less (p trend < 0.001). Adding TTFC to the lung cancer incidence model improved the area under the receiver operating curve by 0.0079 (95% confidence interval = 0.0019-0.0138 [p = 0.0085]). Among 8994 smokers without a lung cancer diagnosis, 180 (2.00%) and 155 (1.67%) more people would be assigned to the no-screening group by adding TTFC to the model (p values for percent changes <0.001) at the 1% and 2% risk thresholds, respectively.
Including TTFC, which can be elicited by a single question at very low cost and noninvasively question, into risk models might better identify smokers with lower risk and could therefore be a safe, convenient tool to improve identification of those who benefit less from lung cancer screening.
基于模型预测风险选择个体已被报道可提高肺癌筛查效率。基于病例对照研究,首次吸烟时间(TTFC)是尼古丁依赖的测量指标,是肺癌风险的一个强有力的独立预测因子。我们的目的是验证前瞻性全国肺癌筛查试验中 TTFC 与肺癌的相关性,并评估是否添加 TTFC 可以改进肺癌风险预测模型。
使用 Cox 模型,我们在 18729 名全国肺癌筛查试验参与者中检查了 TTFC(≤5、6-14、15-29、30-59 和≥60 分钟)与肺癌发病和死亡之间的关联,全面调整了吸烟和其他肺癌风险因素。我们使用没有 TTFC 的模型估计了 5 年个体肺癌发病率,并根据 1%和 2%的风险阈值将其分为筛查或不筛查组。计算了没有和有 TTFC 的模型的受试者工作特征曲线下面积。
TTFC 为 60 分钟或更长时间的吸烟者,标准化的 5 年肺癌发病风险低很多-1.54%(TTFC 60 分钟或更长时间为 1.52%-1.56%,TTFC 5 分钟或更短时间为 4.07%(4.04%-4.09%),肺癌死亡风险低-0.59%(TTFC 60 分钟或更长时间为 0.57%-0.61%,TTFC 5 分钟或更短时间为 2.26%(2.23%-2.28%)(趋势检验 p <0.001)。将 TTFC 添加到肺癌发病模型中,使受试者工作特征曲线下面积增加了 0.0079(95%置信区间 0.0019-0.0138[p=0.0085])。在 8994 名没有肺癌诊断的吸烟者中,通过将 TTFC 添加到模型中,分别有 180(2.00%)和 155(1.67%)人会被分配到不筛查组(p 值<0.001),风险阈值分别为 1%和 2%。
纳入 TTFC(可通过简单的非侵入性问题询问获得)到风险模型中可能更好地识别低风险吸烟者,因此可能是一种安全、方便的工具,可以提高对那些从肺癌筛查中获益较少的人群的识别能力。