- lung cancer screening
- primary health care
- implementation science
- implementation strategies
- practice guidelines
- Preventive Health Services
A man aged 60 years presented to his primary care physician because of a 5-kg unintentional weight loss over 3 months, hemoptysis, and exertional shortness of breath, but no fever. He had smoked 20 to 30 cigarettes a day since his 20s before quitting a year prior because of health concerns. A chest radiograph and computed tomography (CT) scan showed findings consistent with lung cancer with metastasis and diagnosis was confirmed promptly. For this patient, a root-cause analysis may ask if opportunities at prevention or early detection were missed.1 The most effective way to prevent lung cancer is to avoid exposure to carcinogens (tobacco, radon, or particulate matter).2 However, in individuals who unfortunately develop lung cancer, early detection is potentially lifesaving.
In this issue of the Annals, Handy and colleagues report on a lung cancer screening (LCS) program in a network of primary care clinicians in a community-based health system in Portland, Oregon.3 The report suggests that delivery of LCS is feasible in community settings and may achieve comparable process outcomes as the controlled settings of clinical trials.3
Their program provides a useful framework for the primary care clinician’s role and linkages with a multidisciplinary team to manage abnormal findings as depicted in Figure 1.4
Cancers of the lung and bronchus remain the single most common cause of death from cancer in the United States despite steady declines in incidence and mortality over the decades. Lung cancer is projected to cause nearly as many deaths as breast, colorectal, and pancreatic cancers combined in 2020 (135,720 vs 142,940),5,6 and African American men have the highest incidence and mortality of any racial or ethnic group.5 The 5-year survival rate during 2010-2016 for people diagnosed with localized-stage disease is 59% compared with 5.8% with metastatic disease at the time of diagnosis, and without screening, 51% of patients present with metastasis.5 Feasibility studies at the Mayo Clinic,7 and the National Lung Screening Trial (NLST),8 provided the evidence for guidelines endorsing LCS in high-risk people (Table 1).9-19 In 2013, the American Academy of Family Physicians (AAFP) concluded the evidence “insufficient to recommend for or against” LCS.18 The AAFP noted that the NLST was conducted in “medical institutions” with expertise to achieve “low mortality associated with surgical resection of tumors, which may not be reproducible in all settings.” Those concerns are acknowledged in all current guidelines. Although other trials, including the Nederlands-Leuvens Longkanker Screenings ONderzoek (NELSON) and the Italian (MILD) trials, have expanded the evidence base,20,21 controversy remains about the applicability of the evidence or the ability to have the expertise and other systems needed for LCS in community settings.
Key details of trials results, including absolute risks, provide insights about LCS’ potential impact. The NLST randomized selected high-risk participants aged 55-74 years during 2002-2004 at 33 well-equipped medical centers to receive low-dose helical CT (LDCT) (n = 26,722) over 3 rounds or chest radiography (n = 26,732) and followed them through the end of 2009.8 It showed a 20% lung cancer–specific mortality risk reduction (2.47 vs 3.09 deaths per 1,000 person years) in those assigned to LDCT screening after 6.5 years of follow-up.8 One subanalysis reported a 39% mortality risk reduction in African American participants (n = 2,361, hazard ration [HR] = 0.61; 95% CI, 0.37-1.01), suggesting that use of LCS could help reduce health disparities.22 The NELSON trial with men (n = 13,195) and women (n = 2,594) aged 50-74 years showed over 4 rounds of screening a similar effect size (24% mortality risk reduction; 2.50 vs 3.30 deaths per 1,000 person years in screened vs control, respectively) after ≥10 years of follow-up.20 About 56% of lung cancers in the NLST and 68% in NELSON were detected at stage I/II.8,23 Similarly, 70% of the 95 cancers reported by Handy and colleagues and 86% of those detected in a United Kingdom lung screening pilot were diagnosed at stage I/II.3,24 Those findings suggest that LDCT screening in community settings may produce reasonable outcomes.
It is important, however, to understand why current LCS guidelines include caveats on having appropriate expertise and processes. Screening is highly popular and widely advocated due to its presumed potential to prevent premature death. Screening can, however, create an illusion of benefits even when causing a net harm because of temporal dissonance between harms and benefits. Benefits of LDCT derive from accurate identification of only serious lesions and achieving optimal follow-up and treatment outcomes. The “window of net benefit” for LCS is related to quality of LDCT images and quality of interpretation, disease prevalence in the population, patient health status, and the timeliness, safety, and effectiveness of treatment for abnormal screening results.25 Harms due to screening, including death, occur from the test itself or from management of lesions that turned out not to be cancerous (false positives) or are not destined to be fatal during a person’s lifetime (overdiagnosis). Therefore, the harms and benefits of LCS vary depending on the population and setting of screening. Given the same health status, people at lower risk may disproportionately experience overdiagnosis and false-positive results. In the NLST, the benefits of LCS were greatest in people in the highest risk strata, but those patients may also have higher prevalence of comorbid conditions and thus a higher complication rate could undermine the benefits.26 In NLST, the major complication rate was 14%.27 In Handy and colleagues’ report, of 3,402 patients screened, 176 underwent invasive procedures with 23 (13%) procedure-related complications that included 2 deaths.3
False-positive rates (FPR), overdiagnosis, and incidental findings contribute to harms. In NLST, the reported FPR was 27.3% in the first round and, over the 3 rounds of screening, 1.8% of participants without lung cancer underwent invasive procedures for a positive screening result with about 6.5 deaths per 10,000 with false positive results in patients with false-positive results.8 The FPR is relatively modest (1.3 to 12.8%), however, when based on findings that call for immediate follow-up,23,24,28 but the wide range across reports portends similar variation in LCS outcomes in community settings. In the NLST, there were 41 cancers detected per 1,000 people screened, which resulted in 3 averted lung cancer deaths and 4 cancers that may have represented overdiagnosis.27 Estimated overdiagnosis rates also vary widely across studies,29-33 but was reported as 3.1% overall during long-term follow-up on the NLST and 8.9% on the NELSON trial.20,34 Another concern is incidental findings, which were reported in 41% of participants in the Veterans Affairs (VA) program, but clinical implications were unclear.35
Therefore, important questions remain about how LCS may be optimally delivered to underserved urban and rural populations. Although Patient Protection and Affordable Care Act provisions allow full coverage of LCS in primary care, it is substantially underutilized with reported prevalence of only about 6% or less,36-38 and primary care clinicians’ role seems unclear.
When the program described by Handy and colleagues began in 2013, it was led by an oncology-radiology team that managed all screening processes after a primary care clinician referral. In 2015, primary care clinicians assumed responsibility for shared decision-making and placing LDCT orders. A program coordinator conducted smoking counseling, and eligibility verification. This iteration of the program was supported by automated reminders. A multidisciplinary team from oncology, pulmonology, and thoracic surgery reviewed LDCTs with suspicious or highly suspicious findings and made follow-up recommendations back to the primary care clinician.39 The program followed standards for image acquisition, interpretation and reporting, and management of nodules; images were interpreted by radiologists at a tertiary facility.3 This strategy conforms with standards recommended in current guidelines and the Centers for Medicare and Medicaid Services (CMS).9-17,19,40
There are some limitations of Handy and colleagues’ study, including a non-diverse population with only 1% (n = 33) African American and <1% (n = 15) American Indian/Alaska Natives (AI/ANs).3 It does not provide evidence of the effectiveness of LCS during routine primary care delivery and few details are provided on approaches to promote timely follow-up of abnormal screening results.1,41 Information was not provided on the approaches used to systematically identify eligible patients or the number of people who were evaluated or received shared decision making and declined screening or were determined to be ineligible.
Delivery of LCS is hampered by incomplete or inaccurate capture of smoking history and a paucity of valid electronic algorithms for assessing LCS-relevant health status, resulting in a scarcity of reliable estimates of the eligible population and LCS prevalence. Clinical services that are measured, tracked, and incentivized get greater attention and those services which are not incorporated into valid quality metrics, such as National Committee for Quality Assurance (NCQA) performance measures, are often of lesser priority. Integration of LCS into primary care workflow and the development of generally accepted LCS clinical performance metrics (eg, false-positive/recall rates, interval cancers, complications, and 30-day mortality rates), along with incentives, may encourage LCS. Stigma against smoking and lung cancer is widely recognized barrier to care all along the lung cancer care continuum either due to provider bias or patient’s perception and anticipation of discrimination.42 Digital technologies may improve access to shared decision making, smoking cessation, and nodule management in underserved rural, racial/ethnic minority, or low-income communities. These issues require study, ideally through a primary care lens.
Family medicine has a critical role in increasing the reach of LCS. Success in tobacco control has been the primary driver of decreasing lung cancer incidence,5 and family medicine as a discipline has been a leader in smoking cessation and prevention. The longitudinal, comprehensive, team-based care in primary care, including integrated behavioral health, is an ideal setting to improve access to LCS, particularly for underserved populations. Family doctors have long-term relationships with their patients and can help them consider whether lung cancer screening is right for them. However, obstacles to the adoption of this technology hinder uptake and delivery, and a planned implementation approach is needed to assure optimal benefits. Evidence is needed on whether strategies such as telehealth can enable access to LCS in less-resourced settings and mitigate the effects of some social and structural barriers.10,19 The American Academy of Family Physicians (AAFP) can guide the approximately 180,000 family physicians on timeliness, quality, and safety of LCS delivery to build on the gains made from tobacco control. There is no place like family medicine to realize the ideals of lung cancer control, but the engagement of primary care clinicians and support from payers and funding agencies are needed to catalyze the adoption of LCS.
Footnotes
Conflicts of interest: author reports none.
To read or post commentaries in response to this article, see it online at http://www.AnnFamMed.org/content/18/3/196.
Disclaimer: C.A.D. is a member of the US Preventive Services Task Force (USPSTF), but the content is solely the responsibility of the authors and does not necessarily represent the views and policies of the USPSTF.
Funding support: C.A.D. was supported in part by the National Cancer Institute of the National Institutes of Health (NIH) under Award Number R01CA213645.
- Received for publication March 25, 2020.
- Accepted for publication March 25, 2020.
- © 2020 Annals of Family Medicine, Inc.