ISSN: 2161-0711

Journal of Community Medicine & Health Education
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
  • Short Communication   
  • J Community Med Health Educ 9: 651, Vol 9(2)

Optimizing Selection of Candidates for Lung Cancer Screening: Impact of Comorbidity, Frailty and Life Expectancy

Dejana Braithwaite* and Shailesh Advani
Department of Oncology, Georgetown University, Washington, USA
*Corresponding Author: Dejana Braithwaite, Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, 3300 Whitehaven Street, NW, Suite 4100, Washington, DC 20007, USA, Tel: 202-687-7852, Fax: 202-687-8444, Email: dejana.braithwaite@georgetown.edu

Received: 27-Feb-2019 / Accepted Date: 12-Mar-2019 / Published Date: 19-Mar-2019

Background of Lung Cancer Screening

Lung cancer accounts for nearly 27% of incident cancers in the United States and is the leading cause of cancer-related mortality [1]. The overall five-year survival in lung cancer patients is 17% but ranges from 55% for local tumors to 4% for distant tumors [1]. In 2011, the U.S. National Lung Screening Trial (NLST) found that three rounds of annual low-dose computed tomography (LDCT) as compared to chest x-ray reduced lung cancer mortality by 20% among persons 55 to 74 years old with ≥30 pack-years of smoking history and ≤ 15 years since quitting [2]. Based on these results, the United States Preventive Task Force (USPSTF) and Centers for Medicaid Services (CMS) recommend lung cancer screening (LCS) for high risk persons, however, USPSTF recommends screening current and former heavy smokers up to the age of 80 years annually and Medicare limits coverage to adults 55 to 77 years old and requires shared decision making before screening [3-7]. Core elements of this shared decisionmaking process involves discussion of benefits, harms and uncertainties of screening [8]. Because participants enrolled in NLST were younger, better educated, had lower number of comorbid conditions and were more likely to be former smokers as compared to the general population, the real-world evidence regarding the effectiveness of LCS remains unclear [9]. Moreover, uncertainty exists regarding the benefits and harms across diverse population groups, including stopping age for screening due to differences in demographic and clinical characteristics such as the burden of chronic co-existing illness and functional limitations.

What do professional guidelines recommend?

Professional guidelines reflect continued uncertainty regarding the stopping ages for LDCT screening. Whereas the American Society of Clinical Oncology, American College of Chest Physicians (ACCP), American Cancer Society (ACS) and the National Comprehensive Cancer Network (NCCN) guidelines are aligned with the NLST criteria of 77 years as the upper age limit [5,10-12], the United States.

Preventive Services Task Force and the American Association of Thoracic Surgery guidelines raises the cutoff to 80 years [13,14]. Overall, these guidelines offer limited guidance for individualizing lung cancer screening decisions as a function of life expectancy and coexisting illnesses. The American Association for Thoracic Surgery (AATS), ACCP, ACS and NCCN guidelines all incorporate life expectancy into some of their eligibility criteria for lung cancer screening; AATS and NCCN recommend screening among individuals with a 20 pack year smoking history and additional comorbidity that increases the risk of developing lung cancer whereas the ACS recommends that eligible individuals should be “in good health” [5,10,13]. The ACCP explicitly states that individuals with comorbidities that adversely influence the ability to tolerate screendetected findings or early- stage cancer treatment should not be screened [12,15]. Moreover, the American Academy of Family Physicians does not formally endorse LCS.7

Existing evidence on the impact of age, comorbidity and life expectancy on LCS outcomes

Evidence from NLST showed that the aggregate false positive rate in NLST was higher among older adults age 65 years compared to those younger than age 65 (65 and over: 27.7% vs. under 65: 22.0%); a higher proportion of invasive diagnostic procedures after false-positive screening was also observed by age (65 and over: 3.3% vs. under 65: 2.7%) [16]. Potential harms of LDCT screening include but are not limited to false positive results, over diagnosis as well as diagnostic and treatment complications due to older age and comorbidity [17-19].

Further, simulation modeling from the Cancer Intervention and Surveillance Modeling Network (CISNET) revealed that rate of over diagnosis increased with age, and hence stopping at earlier age might provide further benefits; however, this warrants further investigation [20]. This is an issue that was consistent across other trials and models and represents a major concern about developing LCS guidelines for community practices.

Crucially, nearly a third of the estimated 8.6 million LDCT lung cancer screening (LCS) eligible U.S. screening population present with significant chronic conditions (COPD, congestive heart failure, diabetes) [21,22]. In 2017, the American Thoracic Society convened a workshop to identify research gaps and future directions to optimize selection of candidates for lung cancer screening by accounting for coexisting chronic illness [9]. Experts from field of oncology, pulmonology, epidemiology and health services research concluded that competing causes of death, including smoking associated comorbid conditions like chronic-obstructive heart disease and cardiovascular disease, are highly prevalent among LCS eligible populations and may limit long term benefits of lung cancer screening due to their impact on overall health and life expectancy [9]. In the LCS context, Howard et al. also reported that the US population eligible for lung cancer screening may benefit less from early detection than NLST participants due to a higher risk of death from competing causes [22]. This emphasizes the need to obtain baseline information on comorbidities and functional status among screen eligible LCS populations to adequately quantify harms and benefits.

Previous reports from simulation models have identified significant impact of comorbidity and life expectancy in estimating screening harms and benefits and individualizing cancer screening decisions in the elderly [23,24]. While the majority of extant lung cancer risk prediction models rely primarily on age and smoking history, the PLCOM2012 model also includes several comorbid conditions, including COPD [25]. In another modeling analysis to predict life expectancy among high risk patients with COPD in a LCS setting, authors identified that lowering inclusion criteria for smoking packyears for these high risk patients may provide additional benefit in terms of life expectancy in LCS setting [26]. Furthermore, other studies have concluded that screening for smoking-associated comorbidities including COPD and emphysema improves lung cancer detection rates and improves the efficiency of lung cancer screening programs by targeting the highest risk individuals [27-30]. In France, researchers recommend that eligible LCS patients with peripheral arterial disease should be screened with a low dose scanner and confirmed with a blood test to identify non-solid tumor cells at an earlier stage [31].

In Italy, researchers recommend that lung cancer screenings should also evaluate cardiovascular abnormalities that might be relevant to a patient’s current health status [32]. Finally, Katki et al. recently compared stimulation modeling for participant selection using two risk based modeling strategies, and found that risk based modeling that incorporates age, smoking history, family history of lung cancer and the presence of comorbidities resulted in greater number of lung cancer deaths prevented over 5 years as compared to model based on USPSTF recommendation [33]. Finally, empirical evidence from various studies have led to the development of a COPD LCS score, which predicts lung cancer risk among patients with COPD eligible for screening [28,30,34]. On one hand, persons with COPD face a two-fold higher risk of lung cancer than smokers without COPD and may be more likely to benefit from LCS [35-39]. On the other hand, persons with advanced COPD are at a greater risk of complications during evaluation of pulmonary nodules [40] and are more likely to experience respiration-related surgical complications, have a higher 30-day mortality after resection of lung cancer (especially after thoracotomy) [25,41] and have a higher risk of non-lung cancer mortality [39,42]. Hence, it becomes crucial to measure both smoking and non-smoking related comorbidities among LCS populations and quantify benefits and harms associated with continued screening, including evaluation of downstream consequences such as rates of biopsies, surgeries, other treatment and rates of complications. Moreover, the continuing controversy over lung cancer screening indicates a need for quantitative data on benefits and harms in the general population, particularly within subgroupings of patients with varying degrees of life expectancy to guide informed choices [43,44].

What about frailty?

The World Health Organization in the last World Report on Ageing and Health, defined frailty as “an extreme vulnerability to endogenous and exogenous stressors that exposes an individual to a higher risk of negative health related outcomes” [45]. Evaluation of frailty is an important variable for the estimation of risk associated with clinical procedures among older adults [46]. Aging is associated with global decline in physiological reserves, leading to decrease tolerance to stress. Further, frailty is considered to be a marker of aging-associated decline in capacity to tolerate stress associated with chronic diseases leading to combined loss of mobility, sensory functions and cognition [47]. However, the underlining biology of frailty remains complex and multifactorial and includes aging-associated decline in functional status and loss of muscle mass. Frailty on the other hand, comprises of age related decrease in physiological reserves and increased vulnerability to stressors due to disturbances in processes associated with energy metabolism and neuromuscular changes [48].

The underlying mechanism of frailty mimics cachexia caused by disturbances in proportions of body fat, low- levels of leptin and high levels of pro-inflammatory cytokines. Domains that make up the frailty syndrome have been utilized in geriatric research over the years and includes combination of mobility, strength, balance, motor processing, cognition, nutrition, endurance and physical activity [49]. Hence a comprehensive assessment of both physical and cognitive domains helps cover global dimensions of frailty and its impact on health outcomes. Prior studies have highlighted frailty to be associated with poor screening outcomes, [50] response to chemotherapy and overall mortality and morbidity [51,52]. Additionally, frailty has shown to be associated with increased healthcare utilization and falls [53] as well as increased risk of multi-morbidity and polypharmacy and associated adverse events [54,55]. Moreover, as frailty impacts lifeexpectancy, understanding benefits and harms associated with LCS by levels of frailty remains unexplored and needs to be emphasized in future lung cancer screening studies.

Current evidence from community settings and future directions

Recently published studies provide conflicting evidence of success of lung cancer screening in community settings [56-63]. Although a couple studies indicated that screening was feasible and found results similar to those in the NLST [64,58,62], others reported hurdles regarding screening program implementation, including limited resources to manage abnormal findings [59], low patient volumes [60], or unanticipated extensive follow-up of incidental findings [64]. Moreover, limited evidence exists how individuals with limited life expectancy are ascertained in the context of LCS. Assessment of a person’s life expectancy can play a crucial role in identifying high risk individuals with favorable life expectancy that might benefit from early detection, as well as in limiting harms associated with over diagnosis and complications in individuals with limited life expectancy.

The uptake of lung cancer screening among the general population in the United States remains relatively low. Results from national studies show that only 1.9% of 7.6 million eligible current and former smokers underwent LDCT screening in 2016 [65]. Reasons for low uptake are multifactorial: limited knowledge of benefits and harms of LCS among primary care providers, including the presence of competing coexisting illnesses, financial barriers and system-level challenges such as preauthorization requirements, adequate access to specialty providers or low commitment at leadership levels [66,67]. Shared decision-making (SDM) is an important aspect of screening referral widely adopted after the USPSTF and CMS recommendations for the Medicare coverage of LCS [44]. Given that the goal of SDM is to provide patients with sufficient knowledge to make informed decisions about screening, updating current information about screening efficacy and contextualizing decisions in terms of comorbidity, frailty, functional status and life expectancy can help generate a more individualized approach towards improving benefits and reducing harms associated with LCS, especially among older adults with coexisting comorbidities [19].

Conclusion

The margin of benefit of LCS is highly uncertain among older adults with comorbidities and limited life expectancy. Further, LCS has not been empirically proven beneficial in individuals with diminished life expectancy due to comorbidity and those ages over 77 and these factors decrease the potential chance of screening benefit and likely increase the risk of harms. Given the heterogeneity in comorbidity and life expectancy among individuals undergoing LCS, it is important to optimize the selection of candidates for screening, especially among older adults beyond age 77 and with limited comorbidities. Research effort warrant evidence to inform life expectancy-based screening, particularly as screening programs disseminate into community practice.

References

  1. Team NLSTR (2011) Reduced lung-cancer mortality with low-dose computed tomographic screening. N Engl J Med 365: 395-409.
  2. Jacobson FL, Austin JH, Field JK, Jett JR, Keshavjee S, et al. (2012) Development of The American association for thoracic surgery guidelines for low-dose computed tomography scans to screen for lung cancer in North America: Recommendations of The american association for thoracic surgery task force for lung cancer screening and surveillance. J Thorac Cardiovasc Surg 144: 25-32.
  3. Moyer VA (2014) Screening for lung cancer: U.S. preventive services task force recommendation statement. Ann Int Med 160: 330-338.
  4. Wender R, Fontham ET, Barrera E, Colditz GA, Church TR, et al. (2013) American cancer society lung cancer screening guidelines. CA Cancer J Clin 63: 107-117.
  5. Wood DE, Kazerooni EA, Baum SL, Eapen GA, Ettinger DS, et al. (2012) Lung cancer screening. J Natl Compr Canc Netw 10: 240-265.
  6. Doubeni C, Gabler N, Wheeler C, McCarthy AM, Castle PE, et al. (2018) Timely follow-up of positive cancer screening results: A systematic review and recommendations from the PROSPR consortium. CA Cancer J Clin 68: 199-216.
  7. Smith RA, Manassaram‐Baptiste D, Brooks D, Doroshenk M, Fedewa S, et al. (2015) Cancer screening in the United States, 2015: A review of current American cancer society guidelines and current issues in cancer screening. CA Cancer J Clin 65: 30-54.
  8. Rivera MP, Tanner NT, Silvestri GA, Detterbeck FC, Tammemägi MC, et al. (2018) Incorporating coexisting chronic illness into decisions about patient selection for lung cancer screening. An official american thoracic society research statement. Am J Respir Crit Care Med 198: e3-e13.
  9. NCCN Guidelines for Patients (2016) Lung cancer screening. Washington DC: National comprehensive cancer network.
  10. Bach PB, Mirkin JN, Oliver TK, Azzoli CG, Berry DA, et al. (2012) Benefits and harms of CT screening for lung cancer: A systematic review. JAMA 307: 2418-2429.
  11. Wiener RS, Gould MK, Arenberg DA, Au DH, Fennig K, et al. (2015) An official American thoracic society/American college of chest physicians policy statement: implementation of low-dose computed tomography lung cancer screening programs in clinical practice. Am J Respir Crit Care Med 192: 881-891.
  12. Jaklitsch MT, Jacobson FL, Austin JH, Field JK, Jett JR, et al. (2012) The American association for thoracic surgery guidelines for lung cancer screening using low-dose computed tomography scans for lung cancer survivors and other high-risk groups. J Thorac Cardiovasc Surg 144: 33-38.
  13. Ito M, Kanno S, Nosho K, Sukawa Y, Mitsuhashi K, et al. (2015) Association of Fusobacterium nucleatum with clinical and molecular features in colorectal serrated pathway. Int J Cancer 37: 1258-1268.
  14. Mazzone P, Silvestri G, Patel S, Kanne JP, Kinsinger LS, et al. (2017) Screening for lung cancer: CHEST guideline and expert panel report. Chest 153: 954-985.
  15. Pinsky PF, Gierada DS, Hocking W, Patz EF, Kramer BS (2014) National lung screening Trial findings by age: Medicare-eligible versus under-65 population. Ann Int Med 161: 627-633.
  16. Moseson EM, Wiener RS, Golden SE, Au DH, Gorman JD, et al. (2016) Patient and clinician characteristics associated with adherence. A cohort study of veterans with incidental pulmonary nodules. Ann Am Thorac Soc 13: 651-659.
  17. Smith-Bindman R (2010) Is computed tomography safe. N Engl j Med 363: 1-4.
  18. Fabrikant MS, Wisnivesky JP, Marron T, Taioli E, Veluswamy RR (2018) Benefits and challenges of lung cancer screening in older adults. Clin Ther 40: 526-534.
  19. Han SS, Ten Haaf K, Hazelton WD, Munshi VN, Jeon J, et al. (2017) The impact of overdiagnosis on the selection of efficient lung cancer screening strategies. Int J Cancer 140: 2436-2443.
  20. Ma J, Ward EM, Smith R, Jemal A (2013) Annual number of lung cancer deaths potentially avertable by screening in the United States. Cancer 119: 1381-1385.
  21. Howard DH, Richards TB, Bach PB, Kegler MC, Berg CJ (2015) Comorbidities, smoking status, and life expectancy among individuals eligible for lung cancer screening. Cancer 121: 4341-4347.
  22. Lansdorp-Vogelaar I, Gulati R, Mariotto AB, Schechter CB, de Carvalho TM, et al. (2014) Personalizing age of cancer screening cessation based on comorbid conditions: model estimates of harms and benefits. Ann Intern Med 161: 104-112.
  23. Mandelblatt JS, Stout NK, Schechter CB, van den Broek JJ, Miglioretti DL, et al. (2016) Collaborative modeling of the benefits and harms associated with different U.S. breast cancer screening strategies. Ann Intern Med 164: 215-225.
  24. Ten Haaf K, Jeon J, Tammemagi MC, Han SS, Kong CY, et al. (2017) Risk prediction models for selection of lung cancer screening candidates: A retrospective validation study. PLoS Medicine 14: e1002277.
  25. Lowry KP, Gazelle GS, Gilmore ME, Johanson C, Munshi V, et al. (2015) Personalizing annual lung cancer screening for patients with chronic obstructive pulmonary disease: A decision analysis. Cancer 21: 1556-1562.
  26. Sekine Y, Katsura H, Koh E, Hiroshima K, Fujisawa T (2012) Early detection of COPD is important for lung cancer surveillance. Eur Respire J 39: 1230-1240.
  27. Gonzalez J, Marin M, Sanchez-Salcedo P, Zulueta JJ (2016) Lung cancer screening in patients with chronic obstructive pulmonary disease. Ann Transl Med 4: 160.
  28. Sekine Y, Fujisawa T, Suzuki K, Tsutatani S, Kubota K, et al. (2014) Detection of chronic obstructive pulmonary disease in community-based annual lung cancer screening: Chiba chronic obstructive pulmonary disease lung cancer screening study group. Respirology19: 98-104.
  29. Sanchez-Salcedo P, Wilson DO, de-Torres JP, Weissfeld JL, Berto J, et al. (2015) Improving selection criteria for lung cancer screening. The potential role of emphysema. Am J Respir Crit Care Med 191: 924-931.
  30. Lederlin M, Tredaniel J, Priollet P (2015) Why screen for lung cancer in patients with arterial disease?. J Mal Vasc 40: 359-364.
  31. Sverzellati N, Arcadi T, Salvolini L, Dore R, Zompatori M, et al. (2016) Under-reporting of cardiovascular findings on chest CT. Radiol Med 121:190-199.
  32. Katki HA, Kovalchik SA, Berg CD, Cheung LC, Chaturvedi AK (2016) Development and validation of risk models to select ever-smokers for CT lung cancer screening. JAMA 315: 2300-2311.
  33. de-Torres JP, Wilson DO, Sanchez-Salcedo P, Weissfeld JL, Berto J, et al.(2015) Lung cancer in patients with chronic obstructive pulmonary disease. Development and validation of the COPD Lung Cancer Screening Score. Am J Respir Crit Care Med 191: 285-291.
  34. Kovalchik SA, Tammemagi M, Berg CD, Caporaso NE, Riley TL, et al. (2013) Targeting of low-dose CT screening according to the risk of lung-cancer death. N Engl J Med 369: 245-254.
  35. Tammemägi MC, Church TR, Hocking WG, Caporaso NE, Riley TL, et al. (2014) Evaluation of the lung cancer risks at which to screen ever-and never-smokers: Screening rules applied to the PLCO and NLST cohorts. PLoS Med 11: e1001764.
  36. Gonzalez J, Marín M, Sánchez-Salcedo P, Zulueta JJ (2016) Lung cancer screening in patients with chronic obstructive pulmonary disease. Ann Transl Med 4: 160.
  37. de-Torres JP, Marín JM, Casanova C, Pinto-Plata V, Divo M, et al. (2016) Identification of COPD patients at high risk for lung cancer mortality using the COPD-LUCSS-DLCO. Chest 149: 936-942.
  38. Hopkins RJ, Duan F, Chiles C, Greco EM, Gamble GD, et al. (2017) Reduced expiratory flow rate among heavy smokers increases lung cancer risk. Results from the national lung screening trial–American college of radiology imaging network cohort. Ann Am Thorac Soc 14: 392-402.
  39. Wiener RS, Schwartz LM, Woloshin S, Welch HG (2011) Population-based risk for complications after transthoracic needle lung biopsy of a pulmonary nodule: An analysis of discharge records. Ann Intern Med 155: 137-144.
  40. Husain ZA, Kim AW, James BY, Decker RH, Corso CD (2015) Defining the high-risk population for mortality after resection of early stage NSCLC. Clin Lung Cancer 16: e183-e187.
  41. Celli BR, Cote CG, Marin JM, Casanova C, Montes de Oca M, et al. (2004) The body-mass index, airflow obstruction, dyspnea, and exercise capacity index in chronic obstructive pulmonary disease. N Engl J Med 350: 1005-1012.
  42. Gill RR, Jaklitsch MT, Jacobson FL (2016) Controversies in lung cancer screening. J Am Coll Radiol 13: R2-7.
  43. Nanavaty P, Alvarez MS, Alberts WM (2014) Lung cancer screening: Advantages, controversies, and applications. Cancer Control 21: 9-14.
  44. Organization WH (2015) World report on ageing and health. World Health Organization.
  45. Sacco R, Condoluci A, Curto LS, Vincenzo O, Romano R, et al. (2018) A new frailty index as a risk predictor of morbidity and mortality: Its application in a Surgery Unit. Eur J Oncol 23: 41-46.
  46. Balducci L (2007) Aging, frailty, and chemotherapy. Cancer Control 14: 7-12.
  47. Fedarko NS (2011) The biology of aging and frailty. Clin Geriatr Med 27: 27-37.
  48. Ferrucci L, Guralnik JM, Studenski S, Fried LP, Cutler GB, et al. (2004) Designing randomized, controlled trials aimed at preventing or delaying functional decline and disability in frail, older persons: a consensus report. J Am Geriatr Soc 52: 625-634.
  49. Walter LC, Eng C, Covinsky KE (2001) Screening mammography for frail older women. J Gen Intern Med16: 779-784.
  50. Singh BK, Sharma K (2018) To study the factors affecting post-operative morbidity and mortality following surgery in elderly. Ind J Appl Res.
  51. Carey EC, Covinsky KE, Lui LY, Eng C, Sands LP, et al. (2008) Prediction of mortality in community‐living frail elderly people with long‐term care needs. J Am Geriatr Soc 56: 68-75.
  52. Fulop T, Larbi A, Witkowski JM, McElhaney J, Loeb M, et al. (2010) Aging, frailty and age-related diseases. Biogerontology 11: 547-563.
  53. Mangin D, Bahat G, Golomb BA, Mallery LH, Moorhouse P, et al. (2018) International group for reducing inappropriate medication use & polypharmacy (IGRIMUP): Position statement and 10 recommendations for action. Drugs Aging 35: 575-587
  54. Basic D, Shanley C (2015) Frailty in an older inpatient population: Using the clinical frailty scale to predict patient outcomes. J Aging Health 27:670-685.
  55. Percac-Lima S, Ashburner JM, Rigotti NA, Park ER, Chang Y, et al. (2018) Patient navigation for lung cancer screening among current smokers in community health centers a randomized controlled trial. Cancer Med 7: 894-902.
  56. Balinger C, Tolentino JC, Birriel TJ, Marchiagiani RJ, Gilbert V, et al. (2015) Lung cancer screening in a community setting: Medicare patients have similar outcomes to younger patients. J Am Coll Surg.
  57. Cattaneo SM, Meisenberg BR, Geronimo MCM, Bhandari B, Maxted JW, et al.(2018) Lung cancer screening in the community setting. Ann Thorac Surg 105: 1627-1632.
  58. Zeliadt SB, Hoffman RM, Birkby G, Eberth JM, Brenner AT, et al. (2018) Challenges implementing lung cancer screening in federally qualified health centers. Am J Prev Med 54: 568-575.
  59. Henderson LM, Jones LM, Marsh MW, Benefield T, Rivera MP, et al.(2017) Lung cancer screening practices in north carolina CT facilities. J Am Coll Radiol 14: 166-170.
  60. Jacobs CD, Jafari ME (2017) Early results of lung cancer screening and radiation dose assessment by low-dose CT at a community hospital. Clin Lung Cancer 18: e327-e331.
  61. Miller AT, Kruger P, Conner K, Robertson T, Rowley B, et al. (2016) Initial outcomes of a lung cancer screening program in an integrated community health system. J Am Coll Radiol 13: 733-737.
  62. Patel S, Cho A, Lamont A, Klatt-Ellis T (2016) Implementing a community hospital lung cancer screening program: A multidisciplinary program and a standardized reporting system. J Am Coll Radiol 13(2 Suppl): R14-17.
  63. Ledford CJ, Gawrys BL, Wall JL, Saas PD, Seehusen DA (2016) Translating new lung cancer screening guidelines into practice: The experience of one community hospital. J Am Board Fam Med 29: 152-155.
  64. Pham D, Bhandari S, Oechsli M, Pinkston CM, Kloecker GH, et al. (2018) Lung cancer screening rates: Data from the lung cancer screening registry. Am Soc Clin Oncol.
  65. Eberth JM, McDonnell KK, Sercy E, Khan S, Strayer SM, et al. (2018) A national survey of primary care physicians: Perceptions and practices of low-dose CT lung cancer screening. Prev Med Rep 11: 93-99.
  66. Jemal A, Fedewa SA (2017) Lung cancer screening with low-dose computed tomography in the United States-2010 to 2015. JAMA Oncol 3: 1278-1281.

Citation: Braithwaite D, Advani S (2019) Optimizing Selection of Candidates for Lung Cancer Screening: Role of Comorbidity, Frailty and Life Expectancy. J Community Med Health Educ 9: 651.

Copyright: © 2019 Braithwaite AA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Top