S. Spiro, P. Shah, R. Rintoul, J. George, S. Janes, M. Callister, M. Novelli, P. Shaw, G. Kocjan, C. Griffiths, M. Falzon, R. Booton, N. Magee, M. Peake, P. Dhillon, K. Sridharan, A. Nicholson, S. Padley, Magali N. Taylor, Asia Ahmed, J. Allen, Y. Ngai, N. Chinyanganya, V. Ashford-Turner, Sarah Lewis, D. Oukrif, P. Rabbitts, N. Counsell, A. Hackshaw
{"title":"Sequential screening for lung cancer in a high-risk group: randomised controlled trial","authors":"S. Spiro, P. Shah, R. Rintoul, J. George, S. Janes, M. Callister, M. Novelli, P. Shaw, G. Kocjan, C. Griffiths, M. Falzon, R. Booton, N. Magee, M. Peake, P. Dhillon, K. Sridharan, A. Nicholson, S. Padley, Magali N. Taylor, Asia Ahmed, J. Allen, Y. Ngai, N. Chinyanganya, V. Ashford-Turner, Sarah Lewis, D. Oukrif, P. Rabbitts, N. Counsell, A. Hackshaw","doi":"10.1183/13993003.00581-2019","DOIUrl":null,"url":null,"abstract":"Background Low-dose computed tomography (LDCT) screening detects early-stage lung cancer and reduces mortality. We proposed a sequential approach targeted to a high-risk group as a potentially efficient screening strategy. Methods LungSEARCH was a national multicentre randomised trial. Current/ex-smokers with mild/moderate chronic obstructive pulmonary disease (COPD) were allocated (1:1) to have 5 years surveillance or not. Screened participants provided annual sputum samples for cytology and cytometry, and if abnormal were offered annual LDCT and autofluorescence bronchoscopy (AFB). Those with normal sputum provided annual samples. The primary end-point was the percentage of lung cancers diagnosed at stage I/II (nonsmall cell) or limited disease (small cell). Results 1568 participants were randomised during 2007–2011 from 10 UK centres. 85.2% of those screened provided an adequate baseline sputum sample. There were 42 lung cancers among 785 screened individuals and 36 lung cancers among 783 controls. 54.8% (23 out of 42) of screened individuals versus 45.2% (14 out of 31) of controls with known staging were diagnosed with early-stage disease (one-sided p=0.24). Relative risk was 1.21 (95% CI 0.75–1.95) or 0.82 (95% CI 0.52–1.31) for early-stage or advanced cancers, respectively. Overall sensitivity for sputum (in those randomised to surveillance) was low (40.5%) with a cumulative false-positive rate (FPR) of 32.8%. 55% of cancers had normal sputum results throughout. Among sputum-positive individuals who had AFB, sensitivity was 45.5% and cumulative FPR was 39.5%; the corresponding measures for those who had LDCT were 100% and 16.1%, respectively. Conclusions Our sequential strategy, using sputum cytology/cytometry to select high-risk individuals for AFB and LDCT, did not lead to a clear stage shift and did not improve the efficiency of lung cancer screening. While low-dose CT is now preferred for lung cancer screening, our randomised trial of smokers with COPD showed that a proposed sequential policy using sputum testing to select who receives low-dose CT and autofluorescence bronchoscopy was ineffective http://bit.ly/2JZujnx","PeriodicalId":77419,"journal":{"name":"The European respiratory journal. Supplement","volume":"14 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1183/13993003.00581-2019","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The European respiratory journal. Supplement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/13993003.00581-2019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
Abstract
Background Low-dose computed tomography (LDCT) screening detects early-stage lung cancer and reduces mortality. We proposed a sequential approach targeted to a high-risk group as a potentially efficient screening strategy. Methods LungSEARCH was a national multicentre randomised trial. Current/ex-smokers with mild/moderate chronic obstructive pulmonary disease (COPD) were allocated (1:1) to have 5 years surveillance or not. Screened participants provided annual sputum samples for cytology and cytometry, and if abnormal were offered annual LDCT and autofluorescence bronchoscopy (AFB). Those with normal sputum provided annual samples. The primary end-point was the percentage of lung cancers diagnosed at stage I/II (nonsmall cell) or limited disease (small cell). Results 1568 participants were randomised during 2007–2011 from 10 UK centres. 85.2% of those screened provided an adequate baseline sputum sample. There were 42 lung cancers among 785 screened individuals and 36 lung cancers among 783 controls. 54.8% (23 out of 42) of screened individuals versus 45.2% (14 out of 31) of controls with known staging were diagnosed with early-stage disease (one-sided p=0.24). Relative risk was 1.21 (95% CI 0.75–1.95) or 0.82 (95% CI 0.52–1.31) for early-stage or advanced cancers, respectively. Overall sensitivity for sputum (in those randomised to surveillance) was low (40.5%) with a cumulative false-positive rate (FPR) of 32.8%. 55% of cancers had normal sputum results throughout. Among sputum-positive individuals who had AFB, sensitivity was 45.5% and cumulative FPR was 39.5%; the corresponding measures for those who had LDCT were 100% and 16.1%, respectively. Conclusions Our sequential strategy, using sputum cytology/cytometry to select high-risk individuals for AFB and LDCT, did not lead to a clear stage shift and did not improve the efficiency of lung cancer screening. While low-dose CT is now preferred for lung cancer screening, our randomised trial of smokers with COPD showed that a proposed sequential policy using sputum testing to select who receives low-dose CT and autofluorescence bronchoscopy was ineffective http://bit.ly/2JZujnx
背景:低剂量计算机断层扫描(LDCT)筛查发现早期肺癌并降低死亡率。我们提出了一种针对高危人群的顺序方法,作为一种潜在的有效筛查策略。方法LungSEARCH是一项国家多中心随机试验。患有轻度/中度慢性阻塞性肺疾病(COPD)的当前/已戒烟者按1:1的比例分为5年监测组或不监测组。筛选的参与者每年提供痰样本进行细胞学和细胞术检查,如果异常,每年提供LDCT和自身荧光支气管镜检查(AFB)。痰液正常者每年提供一次样本。主要终点是诊断为I/II期(非小细胞)或有限疾病(小细胞)的肺癌的百分比。结果:2007-2011年间,从英国10个中心随机抽取1568名参与者。85.2%的筛查者提供了足够的基线痰样本。785名筛查者中有42人患肺癌,783名对照者中有36人患肺癌。54.8%(42人中有23人)的筛查个体与45.2%(31人中有14人)的已知分期的对照组被诊断为早期疾病(单侧p=0.24)。早期和晚期癌症的相对危险度分别为1.21 (95% CI 0.75-1.95)和0.82 (95% CI 0.52-1.31)。痰液的总体敏感性(随机纳入监测组)较低(40.5%),累积假阳性率(FPR)为32.8%。55%的癌症患者在整个过程中痰结果正常。在痰液阳性的AFB患者中,敏感性为45.5%,累积FPR为39.5%;LDCT患者的相应措施分别为100%和16.1%。我们的序贯策略,使用痰细胞学/细胞术选择高危人群进行AFB和LDCT,并没有导致明显的阶段转移,也没有提高肺癌筛查的效率。虽然低剂量CT现在是肺癌筛查的首选,但我们对COPD吸烟者的随机试验表明,使用痰液检测来选择接受低剂量CT和自身荧光支气管镜检查的患者的顺序策略是无效的http://bit.ly/2JZujnx