Division of Thoracic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Department of Epidemiology and Population Health, Stanford, CA, USA.
BMJ. 2022 Mar 30;376:e069008. doi: 10.1136/bmj-2021-069008.
To determine the effect of the introduction of low dose computed tomography screening in 2013 on lung cancer stage shift, survival, and disparities in the stage of lung cancer diagnosed in the United States.
Quasi-experimental study using Joinpoint modeling, multivariable ordinal logistic regression, and multivariable Cox proportional hazards modeling.
US National Cancer Database and Surveillance Epidemiology End Results program database.
Patients aged 45-80 years diagnosed as having non-small cell lung cancer (NSCLC) between 1 January 2010 and 31 December 2018.
Annual per cent change in percentage of stage I NSCLC diagnosed among patients aged 45-54 (ineligible for screening) and 55-80 (potentially eligible for screening), median all cause survival, and incidence of NSCLC; multivariable adjusted odds ratios for year-to-year changes in likelihood of having earlier stages of disease at diagnosis and multivariable adjusted hazard ratios for changes in hazard of death before versus after introduction of screening.
The percentage of stage I NSCLC diagnosed among patients aged 55-80 did not significantly increase from 2010 to 2013 (from 27.8% to 29.4%) and then increased at 3.9% (95% confidence interval 3.0% to 4.8%) per year from 2014 to 2018 (from 30.2% to 35.5%). In multivariable adjusted analysis, the increase in the odds per year of a patient having one lung cancer stage lower at diagnosis during the time period from 2014 to 2018 was 6.2% (multivariable adjusted odds ratio 1.062, 95% confidence interval 1.048 to 1.077; P<0.001) higher than the increase in the odds per year from 2010 to 2013. Similarly, the median all cause survival of patients aged 55-80 did not significantly increase from 2010 to 2013 (from 15.8 to 18.1 months), and then increased at 11.9% (8.9% to 15.0%) per year from 2014 to 2018 (from 19.7 to 28.2 months). In multivariable adjusted analysis, the hazard of death decreased significantly faster after 2014 compared with before 2014 (P<0.001). By 2018, stage I NSCLC was the predominant diagnosis among non-Hispanic white people and people living in the highest income or best educated regions. Non-white people and those living in lower income or less educated regions remained more likely to have stage IV disease at diagnosis. Increases in the detection of early stage disease in the US from 2014 to 2018 led to an estimated 10 100 averted deaths.
A recent stage shift toward stage I NSCLC coincides with improved survival and the introduction of lung cancer screening. Non-white patients and those living in areas of greater deprivation had lower rates of stage I disease identified, highlighting the need for efforts to increase access to screening in the US.
确定 2013 年低剂量计算机断层扫描筛查的引入对美国肺癌分期转移、生存和诊断肺癌分期差异的影响。
使用 Joinpoint 建模、多变量有序逻辑回归和多变量 Cox 比例风险模型进行准实验研究。
美国国家癌症数据库和监测、流行病学和最终结果计划数据库。
2010 年 1 月 1 日至 2018 年 12 月 31 日期间诊断为非小细胞肺癌(NSCLC)的 45-80 岁患者。
45-54 岁(不符合筛查条件)和 55-80 岁(可能有资格接受筛查)患者中 I 期 NSCLC 诊断比例的年变化百分比、所有原因中位生存时间以及 NSCLC 的发病率;多变量调整后诊断时疾病分期较早的可能性逐年变化的比值比和引入筛查前后死亡风险变化的多变量调整风险比。
2010 年至 2013 年,55-80 岁患者中 I 期 NSCLC 的诊断比例从 27.8%增加到 29.4%,然后从 2014 年至 2018 年以每年 3.9%(95%置信区间 3.0%至 4.8%)的速度增加(从 30.2%增加到 35.5%)。多变量调整分析显示,2014 年至 2018 年期间,患者每年有一个更低肺癌分期的可能性每年增加 6.2%(多变量调整比值比 1.062,95%置信区间 1.048 至 1.077;P<0.001),高于 2010 年至 2013 年期间的可能性每年增加。同样,55-80 岁患者的所有原因中位生存时间从 2010 年至 2013 年没有显著增加(从 15.8 个月增加到 18.1 个月),然后从 2014 年至 2018 年以每年 11.9%(8.9%至 15.0%)的速度增加(从 19.7 个月增加到 28.2 个月)。多变量调整分析显示,2014 年后死亡风险显著降低(P<0.001)。到 2018 年,I 期 NSCLC 是非西班牙裔白人和生活在收入最高或教育程度最好地区的人的主要诊断。非白人患者和生活在收入较低或教育程度较低地区的患者在诊断时更有可能患有 IV 期疾病。美国从 2014 年到 2018 年对早期疾病的检测增加,估计避免了 10000 人死亡。
最近向 I 期 NSCLC 的分期转移与生存改善和肺癌筛查的引入相吻合。非白人和生活在贫困地区的患者,I 期疾病的检出率较低,这突出表明需要努力增加美国的筛查机会。