Kvale Paul A, Johnson Christine Cole, Tammemägi Martin, Marcus Pamela M, Zylak Carl J, Spizarny David L, Hocking William, Oken Martin, Commins John, Ragard Lawrence, Hu Ping, Berg Christine, Prorok Philip
Division of Pulmonary and Critical Care Medicine, Henry Ford Health System, Detroit, MI, United States.
Department of Public Health Sciences, Henry Ford Health System, Detroit, MI, United States.
Lung Cancer. 2014 Oct;86(1):41-6. doi: 10.1016/j.lungcan.2014.07.013. Epub 2014 Jul 24.
The Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial provides us an opportunity to describe interval lung cancers not detected by screening chest X-ray (CXR) compared to screen-detected cancers.
Participants were screened for lung cancer with CXR at baseline and annually for two (never smokers) or three (ever smokers) more years. Screen-detected cancers were those with a positive CXR and diagnosed within 12 months. Putative interval cancers were those with a negative CXR screen but with a diagnosis of lung cancer within 12 months. Potential interval cancers were re-reviewed to determine whether lung cancer was missed and probably present during the initial interpretation or whether the lesion was a "true interval" cancer.
77,445 participants were randomized to the intervention arm with 70,633 screened. Of 5227 positive screens from any screening round, 299 resulted in screen-detected lung cancers; 151 had potential interval cancers with 127 CXR available for re-review. Cancer was probably present in 45/127 (35.4%) at time of screening; 82 (64.6%) were "true interval" cancers. Compared to screen-detected cancers, true interval cancers were more common among males, persons with <12 years education and those with a history of smoking. True interval lung cancers were more often small cell, 28.1% vs. 7.4%, and less often adenocarcinoma, 25.6% vs. 56.2% (p<0.001), more advanced stage IV (30.5% vs. 16.6%, p<0.02), and less likely to be in the right upper lobe, 17.1% vs. 36.1% (p<0.02).
True interval lung cancers differ from CXR-screen-detected cancers with regard to demographic variables, stage, cell type and location. ClinicalTrials.gov number: NCT00002540.
前列腺、肺、结肠直肠和卵巢癌筛查试验为我们提供了一个机会,来描述与筛查发现的癌症相比,未通过胸部X线(CXR)筛查发现的间期肺癌。
参与者在基线时接受CXR肺癌筛查,此后从未吸烟者每年筛查两年,曾经吸烟者每年筛查三年。筛查发现的癌症是指CXR结果为阳性且在12个月内确诊的癌症。假定的间期癌症是指CXR筛查结果为阴性但在12个月内被诊断为肺癌的癌症。对潜在的间期癌症进行重新评估,以确定肺癌在初次解读时是否被漏诊且可能已经存在,或者该病变是否为“真正的间期”癌症。
77445名参与者被随机分配到干预组,其中70633人接受了筛查。在任何一轮筛查的5227次阳性结果中,299例导致筛查发现肺癌;151例有潜在的间期癌症,其中127例CXR可供重新评估。在筛查时,45/127(35.4%)可能已经存在癌症;82例(64.6%)为“真正的间期”癌症。与筛查发现的癌症相比,真正的间期癌症在男性、受教育年限<12年的人群以及有吸烟史的人群中更为常见。真正的间期肺癌更常为小细胞癌,分别为28.1%和7.4%,腺癌则较少见,分别为25.6%和56.2%(p<0.001),更常处于IV期晚期(30.5%和16.6%,p<0.02),且较少位于右上叶,分别为17.1%和36.1%(p<0.02)。
真正的间期肺癌在人口统计学变量、分期、细胞类型和位置方面与CXR筛查发现的癌症不同。ClinicalTrials.gov编号:NCT00002540。