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      Strange Bedfellows: The Interaction between COPD and Lung Cancer in the Context of Lung Cancer Screening

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          Abstract

          It has been nearly 70 years since Doll first described the association between cigarette smoking and lung cancer (1), and later others followed by discovering the association of smoking with chronic obstructive pulmonary disease (COPD). Some smokers suffer the unfortunate “double whammy” of having preexisting COPD that increases the risk of developing lung cancer and are diagnosed with both. More recently, screening high-risk current and former smokers for lung cancer using radiation low-dose computed tomography (CT) has been added to the mix (2, 3). As screening is implemented globally, and given the increased risk of developing lung cancer in those suffering from COPD, there is a temptation to advocate screening all eligible patients with COPD with the hope of enriching the screened population with more patients likely to develop an early, curable cancer. To test that hypothesis in those eligible for screening, it would be important to know the prevalence and severity of COPD, the presence of respiratory symptoms, and the prevalence of other comorbid conditions to better understand their effect on screening outcomes. The study by Ruparel and colleagues (pp. 869–878) published in this issue of AnnalsATS goes some way to providing that information (4). The study design was clever. Nearly 8,000 patients eligible for lung cancer screening by age, smoking history, or meeting certain thresholds for developing lung cancer using validated lung cancer risk models were invited to participate in a “lung health check,” rather than just being offered a chest CT screen (4). In addition to a detailed medical history, they all had spirometry. Perhaps one of the most important aspects of this study was that it was undertaken in underserved communities, as evidenced by the fact that more than half had left school before the age of 15 years and there was a higher proportion than expected of current heavy smokers. These communities are where lung cancer screening is likely to have the most impact. The findings were eye opening, with more than half of the participants having spirometric evidence of COPD. Surprisingly, two-thirds of those did not have a documented prior history of the disease. Not surprisingly, the odds of having respiratory symptoms increased significantly as airflow obstruction worsened, and the presence of comorbidities was significantly higher in those with known versus undiagnosed COPD. Now comes the tricky part. How do we convert the knowledge gained from this study into our practice of screening for lung cancer? We know that the risk of lung cancer increases in a linear relationship as the severity of airflow limitation worsens, which means those at greatest risk of lung cancer generally have the highest prevalence of COPD (5, 6). This observation underpins an important limitation of using a risk-based (i.e., age and pack-year history) approach to selecting smokers for screening. Increasing age and smoking history not only increases the likelihood of developing lung cancer but also increases the likelihood of getting COPD. This is important because COPD is associated with a number of other smoking-related diseases, such as coronary artery disease, and is a strong marker of reduced life expectancy among smokers (7–9). This translates to reduced gains from screening. Indeed a post hoc analysis of the NLST (National Lung Screening trial) reported that for those with COPD (the presence of airflow limitation on the basis of spirometry), the reduction in lung cancer mortality associated with the CT arm relative to the chest radiograph arm was about 15%, in contrast to those with normal lung function, where the reduction in lung cancer mortality was 28%, nearly twofold greater (6). In a further post hoc analysis, this reduced benefit for those with COPD was linked to lower surgical rates for early-stage cancer and greater deaths from non–lung cancer causes (6). In the same analysis, there was no screening benefit in those with Global Initiative for Chronic Obstructive Lung Disease 3 or 4 severity (6). These findings suggest that underlying (and unrecognized) COPD may contribute to both undertreatment, where surgery is inappropriately withheld, and overtreatment, where surgery is undertaken but no survival benefit is achieved. Another feature of having preexisting COPD in the context of lung cancer is that it is associated with more aggressive forms of lung cancer (10). This means more aggressive biology reflected in both histology (more small-cell, squamous-cell, and non–small-cell subtypes) and shorter volume-doubling times (10, 11). This suggests that lung cancers developing in those with advanced COPD may be less amenable to early diagnosis by screening and confer only modest long-term survival after surgery (6). If reducing lung cancer mortality and prolonging survival are the key determinants of successful screening, then it is likely that screening those at intermediate risk where life expectancy is greater (than for those at high risk) may be a more cost-efficient way to undertake screening. Although the routine use of spirometry in the setting of lung cancer screening may identify those with significant airflow limitation and greatest risk of lung cancer, it may have a greater utility in identifying who has severely limited life expectancy and who gains little from screening for lung cancer (e.g., Global Initiative for Chronic Obstructive Lung Disease 3–4 COPD) (6). In other words selection using a solely “risk-based” approach, with the aim to enrich the number of lung cancers identified through screening, may not improve the risk–benefit balance, particularly where the benefit ignores long-term survival. Recently, Cheung and colleagues developed a life-years–gained model, compared it to traditional risk-based screening, and found that using their approach would maximize the benefits of screening by including patients who have both a high risk of developing lung cancer and a long life expectancy (12). Although all of these machinations seem like an exercise built for ivory tower academics, the reality on the ground is that <10% of those eligible for screening in the United States have been screened (13–15). Although spirometry is likely to be helpful in assessing a patient’s risk of developing lung cancer and may provide information regarding the risk/benefit ratio from screening, one has to question whether it is feasible to add spirometry to a visit that already includes a shared decision-making component and a smoking cessation consultation for current smokers. Still, the concept of a “lung health check” is intriguing, as it may provide a forum for checking a patient for both COPD and lung cancer and present an opportunity for smoking cessation counseling to those with newly diagnosed disease. Following this cohort is critical, as it will add to our knowledge of how to interpret the effect COPD has on the outcomes of lung cancer screening and whether upfront spirometry should become a routine part of the screening visit. Stay tuned. Supplementary Material Supplements Author disclosures

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          Most cited references11

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          Forced expiratory volume in one second: not just a lung function test but a marker of premature death from all causes.

          The clinical utility of spirometric screening of asymptomatic smokers for early signs of air flow limitation has recently come under review. The current authors propose that reduced forced expiratory volume in one second (FEV(1)) is more than a measure of airflow limitation, but a marker of premature death with broad utility in assessing baseline risk of chronic obstructive pulmonary disease (COPD), lung cancer, coronary artery disease and stroke, collectively accounting for 70-80% of premature death in smokers. Reduced FEV(1) identifies undiagnosed COPD, has comparable utility to that of serum cholesterol in assessing cardiovascular risk and defines those smokers at greatest risk of lung cancer. As such, reduced FEV(1) should be considered a marker that identifies smokers at greatest need of medical intervention. Smoking cessation has been shown to attenuate FEV(1) decline and, if achieved before the age of 45-50 yrs, may not only preserve FEV(1) within normal values but substantially reduce cardiorespiratory complications of smoking. Recent findings suggest inhaled drugs (bronchodilators and corticosteroids), and possibly statins, may be effective in reducing morbidity and mortality in patients with chronic obstructive pulmonary disease. The current authors propose that spirometry has broad utility in identifying smokers who are at greatest risk of cardiorespiratory complications and greatest benefit from targeted preventive strategies, such as smoking cessation, prioritised screening and effective pharmacotherapy.
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            Lung Cancer Screening Utilization: A Behavioral Risk Factor Surveillance System Analysis

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              Life expectancy and years of life lost in chronic obstructive pulmonary disease: Findings from the NHANES III Follow-up Study

              Rationale Previous studies have demonstrated that chronic obstructive pulmonary disease (COPD) causes increased mortality in the general population. But life expectancy and the years of life lost have not been reported. Objectives To quantify mortality, examine how it varies with age, sex, and other risk factors, and determine how life expectancy is affected. Methods We constructed mortality models using the Third National Health and Nutrition Examination Survey, adjusting for age, sex, race, and major medical conditions. We used these to compute life expectancy and the years of life lost. Measurements and main results Pulmonary function testing classified patients as having Global Initiative on Obstructive Lung Disease (GOLD) stage 0, 1, 2, 3 or 4 COPD or restriction. COPD is associated with only a modest reduction in life expectancy for never smokers, but with a very large reduction for current and former smokers. At age 65, the reductions in male life expectancy for stage 1, stage 2, and stages 3 or 4 disease in current smokers are 0.3 years, 2.2 years, and 5.8 years. These are in addition to the 3.5 years lost due to smoking. In former smokers the reductions are 1.4 years and 5.6 years for stage 2 and stages 3 or 4 disease, and in never smokers they are 0.7 and 1.3 years. Conclusions Persons with COPD have an increased risk of mortality compared to those who do not, with consequent reduction in life expectancy. The effect is most marked in current smokers, and this is further reason for smokers to quit.
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                Author and article information

                Journal
                Ann Am Thorac Soc
                Ann Am Thorac Soc
                AnnalsATS
                Annals of the American Thoracic Society
                American Thoracic Society
                2329-6933
                2325-6621
                July 2020
                July 2020
                July 2020
                : 17
                : 7
                : 810-812
                Affiliations
                [ 1 ]Division of Pulmonary and Critical Care Medicine, Medical University of South Carolina, Charleston, South Carolina; and
                [ 2 ]University of Auckland, Auckland, New Zealand
                Article
                202005-433ED
                10.1513/AnnalsATS.202005-433ED
                7328173
                32609030
                96346fe5-0574-454b-9d2d-4e5dc950b8bc
                Copyright © 2020 by the American Thoracic Society

                This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 ( http://creativecommons.org/licenses/by-nc-nd/4.0/). For commercial usage and reprints, please contact Diane Gern ( dgern@ 123456thoracic.org ).

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