ABSTRACT
Asbestos was largely used in Brazil. It is a mineral that induces pleural and pulmonary fibrosis, and it is a potent carcinogen. Our objective was to develop recommendations for the performance of adequate imaging tests for screening asbestos-related diseases. We searched peer-reviewed publications, national and international technical documents, and specialists' opinions on the theme. Based on that, the major recommendations are: Individuals exposed to asbestos at the workplace for = 1 year or those with a history of environmental exposure for at least 5 years, all of those with a latency period > 20 years from the date of initial exposure, should initially undego HRCT of the chest for investigation. Individuals with pleural disease and/or asbestosis should be considered for regular lung cancer monitoring. Risk calculators should be adopted for lung cancer screening, with a risk estimate of 1.5%.
Keywords:
Asbestosis/diagnosis; Asbestosis/prevention & control; Environmental exposure; Occupational exposure.
INTRODUCTION Asbestos is a general term that refers to a heterogeneous group of natural minerals that occur in the form of fibers (length to diameter ratio ≥3:1), mostly composed of hydrated magnesium silicates and a variable content of other cations such as iron, aluminum, and sodium.(1)
Asbestos has been employed in different production sectors of the manufacturing industry due to its physical and chemical properties of heat resistance, even in high temperatures, low density, flexibility, mechanical and chemical resistance, and also because of its low cost.
Inhaled fibers can cause a spectrum of diseases, including lung cancer; malignant mesothelioma of the pleura, peritoneum, pericardium, and tunica vaginalis; laryngeal and ovarian cancers; nonmalignant pleural diseases; asbestosis; and airflow obstruction.(2,3) Less consistent evidence has shown that they are associated with a higher incidence of retroperitoneal fibrosis.(3) Asbestos exposure is the main risk factor for occupational cancer globally and a significant cause of disease and disability.(4)
The incidence and prevalence of those diseases are intimately related to occupational and environmental exposure to asbestos, such as workers in asbestos mining and processing, as well as workers in industries of manufactured goods such as asbestos-cement, automotive parts, textile products, thermal insulation materials, and others. Relatives of exposed workers and people living in communities surrounding mining and industrial areas also face risk of exposure.(5,6)
There are no serological markers nor other types of markers for the early diagnosis of the diseases related to asbestos exposure mentioned above. For pleuropulmonary diseases, the object of the present document, chest imaging is the detection method used globally.
In Brazil, despite efforts to restrict asbestos production and use, the number of reported cases of asbestos-related diseases is still much lower than the estimates,(7,8) which strengthens the need to develop structured programs for the screening of these diseases featuring the incorporation of more sensitive imaging methods such as chest CT.(9-13)
OBJECTIVE To develop recommendations for the screening of pleuropulmonary diseases related to asbestos exposure through the performance of imaging tests.
METHODS A narrative review of the literature of diagnostic imaging of nonmalignant asbestos-related diseases and lung cancer screening in asbestos-exposed individuals was elaborated. The literature used in the development of this document encompassed peer-reviewed publications and documents from national and international institutions. Based on this narrative review, a panel of specialists composed of pulmonologists and a radiologist with expertise in the field proposed recommendations for the diagnosis and monitoring of asbestos-exposed individuals.
EPIDEMIOLOGY Asbestos exposure is one of the main occupational risk factors for respiratory diseases and has the greatest impact on morbidity and mortality. Global estimates for 2019 reveal that 239.3 thousand deaths and 4.189 million disability-adjusted life-years derive from asbestos exposure.(4) The greatest impact is associated with lung cancer, in which asbestos accounts for approximately 10% of global deaths, not to mention thousands of cases of mesothelioma of serous membranes diagnosed on an annual basis.(4,14) Global estimates for the same year suggest that lung cancer has the highest incidence (2.26 million) and the highest mortality (2.04 million) among cancers.(4,15)
In Brazil, a cross-sectional study involving former asbestos-cement workers who had been employed predominantly in the 1960s and 1970s found a high prevalence of nonmalignant asbestos-related diseases and a progressive reduction in prevalence among those employed in the 1980s,(16) a predictable trend due to pressures for asbestos ban, which caused a slow reduction in asbestos use. Data from other countries(17) and global data(14) have indicated a slower reduction in mortality, varying between countries and with a greater predicted impact from 2030 onwards. An ecological study suggested greater mortality due to lung cancer in men and women, from mesothelioma in men, and from ovarian cancer in women in a cluster of municipalities that housed asbestos-cement factories and/or asbestos mining in Brazil,(18) corroborating another study that found evidence of an important underreporting of cases of asbestos-related diseases in the country.(19)
It is important to bear in mind that smoking is the main risk factor for lung cancer, followed by asbestos exposure and air pollution,(4,15) and it is well established that exposure to asbestos and tobacco smoke presents a positive synergism, that is, the associated risk of both exposures is higher than the sum of the respective risks for lung cancer incidence.(20,21) The prevalence of the sum of smokers and former smokers in Brazil and globally exceeds 40% of the population older than 18 years, being higher in the male sex,(22,23) that is, a large number of adult workers may have been exposed to the two risk factors: asbestos and smoking.
Studies indicate that occupational asbestos exposure is associated with a relative risk for lung cancer incidence that is 2 to 10 times higher compared with the general population, and has a dose-response relationship with fiber concentration in the work environment and cumulative exposure,(24) not to mention the synergistic effect with other carcinogens, such as those present in tobacco smoke.(20)
IMAGING METHODS Chest radiography is the exam required by the Brazilian legislation on occupational safety and medicine(25) for the periodical monitoring of workers exposed to mineral dust. Periodical chest radiographs have the advantages of standardized interpretation through the International Labour Organization’s International Classification of Radiographs of Pneumoconioses criteria(26) and low radiation dose. Although it is widely used and complies with the Brazilian legislation on occupational safety,(25) chest radiography has lost relevance with the advent of CT, especially with the drastic reduction in ionizing radiation enabled by the new tomography machines.(27)
It is well established that chest CT is more sensitive for the diagnosis of diseases related to asbestos exposure.(9,13) HRCT, including low-dose CT of the chest,(28) provides a more accurate diagnosis of interstitial lung diseases, such as asbestosis, and that of pleural thickening, such as pleural plaques. Furthermore, it is more indicated for the early diagnosis of pulmonary nodules. Between 20% and 50% of pleural abnormalities visualized in autopsies and CT scans are not visualized in radiographs, and 15-30% of individuals with radiographs interpreted as normal present abnormalities suggestive of asbestosis on HRCT. In addition to greater sensitivity and specificity, chest HRCT also presents lower variability between experienced chest radiograph readers compared with radiography.(2,9-13,16,29) The patterns of tomographic images also allow to enhance the differential diagnosis between asbestosis and interstitial lung diseases of other etiologies(30,31) and a greater accuracy in the identification of pulmonary nodules.(32,33)
In the current scenario, most individuals exposed to asbestos have lower exposure doses because they started working in the 1980s, the decade when movements and actions to restrict and eliminate asbestos use began. Even though such movements and actions had a reduced reach, they succeeded in bringing about improved environmental control and prohibiting the use of amphiboles. As a consequence, exposed individuals may present subtle abnormalities, both in the pleura and in the parenchyma. In addition, individuals with a smoking history, emphysema, and/or chronic bronchitis or other tobacco-related lung diseases, advanced age, heart failure, obesity, and other exposures to dust or particles may present radiographic abnormalities that hinder the adequate identification of asbestosis and reduce the accuracy of interpretation.(2,13,30,31,34,35)
Specialty societies in the thoracic area have long been indicating the use of chest HRCT to diagnose interstitial lung diseases.(36) Therefore, there is no justification for indicating HRCT for the diagnosis and monitoring of interstitial diseases in general and restricting it in the case of occupational interstitial diseases like asbestosis.
On the other hand, the identification of nonmalignant abnormalities, especially asbestosis,(21) but also pleural plaques,(37,38) enables to evaluate the inclusion of these individuals in the high-risk group for developing lung cancer and to ensure that they are monitored.
Furthermore, studies carried out in the past 20 years have shown that the sensitivity of low-dose HRCT (LD-HRCT) to detect interstitial lung abnormalities is apparently similar to that of conventional thin-slice tomography (HRCT), and both of them are superior to the older, initial conventional tomography,(38-42) with lower exposure to radiation. A study involving 2,760 nuclear weapons workers potentially exposed to asbestos found that LD-HRCT enabled the detection of 3.7 times more pleural plaques and five times more interstitial lung diseases than chest radiography.(33)
These results stimulated the conduction of studies focusing on long-term screening for the early diagnosis of lung cancer,(25) which demands repeated tests with the use of LD-HRCT and, more recently, ultra-LD-HRCT. (41-44) In the past, the radiation dose from a conventional chest tomography used to be higher than the dose from 100 chest X-rays. Comparative studies have shown that exposure per exam has been reduced with the use of low-dose helical tomography equipped with a higher number of detectors (32 or more) and new algorithms for image reconstruction. Such studies have found radiation exposures, measured in millisieverts (mSv), of 0.16 mSv and 1-2 mSv from ultra-low-dose HRCT and low-dose HRCT, respectively, compared with 0.05 mSv and 0.24 mSv from lateral and posteroanterior chest X-ray, images being acquired with appropriate quality.(43-46) The risk of HRCT is not zero, but it is much lower than the benefits related to the reduction in mortality by lung cancer revealed by many studies conducted with risk populations. Although it is not possible to produce accurate estimates, estimated risk(47) is calculated based on the radiation effects of the exposure to the atomic bombs in Hiroshima and Nagasaki. Thus, the estimated risk is that the annual exposure of an individual from the age of 50 to the age of 75 years to LD-HRCT radiation is 1.8% (95% CI: 0.5-5.5%), much lower than the mortality reduction found in different studies, which ranges between 15% and 30%.(27,48-50)
As studies have shown a favorable inclination towards the utilization of HRCT in lung cancer screening, its use started to be recommended in the USA,(48-50) in European countries,(51) by Collegium Ramazzini,(27) and, recently, by the Brazilian Thoracic Society,(52) for individuals who meet the criteria suggested in the studies, centered on the main risk factor: smoking. One of the concerns in screening studies is the overdiagnosis of non-neoplastic nodules, leading to procedures that have a negative impact on patients. However, analyses of many international and Brazilian studies have shown only a few relevant complications and that the benefits outweigh the risks.(50-52)
The lung cancer risk of individuals with a history of occupational asbestos exposure is comparable to or higher than that of individuals who meet the classic eligibility criteria for lung cancer screening programs with LD-HRCT(49,53,54) even if they have been former smokers for more than 15 years or have smoked less than 20 pack-years. A recent guideline from the American Cancer Society(49,50) recommends, among other updates, that the number of years since smoking cessation should not be one more eligibility criterion for inclusion in screening programs, which is something that other studies, such as those that suggest the use of risk calculators,(55-57) already do.
A model developed in England to assess risk prediction based on a cohort study involving more than 18 million individuals revealed that asbestos exposure is one of the main risk prediction factors for lung cancer.(57)
RECOMMENDATIONS 1. For all individuals with a history of occupational exposure to asbestos for at least one year, or domestic exposure (workers’ relatives exposed through clothes that are likely to be contaminated or exposed to asbestos products brought for use inside the domicile) or environmental exposure (individuals living near mining companies or factories involved in the manufacture of asbestos products) for at least five years, with 20 years’ latency or over, the recommendation is that, apart from clinical, functional assessment, and the necessary compliance with the labour rules for periodical examination, when needed, they should be submitted to an HRCT of the chest as the first imaging test (Table 1).
Based on the findings obtained through the images and on clinical and functional aspects, the individuals can be followed up through criteria defined according to the potential risk, as follows:
1.1. Individuals aged 50 or older up to 75 years of age presenting pleural plaques and/or diffuse pleural thickening, with or without round atelectasis, and/or signs compatible with asbestosis, mainly presence of subpleural dots and lines, interlobular septal thickening, parenchymal bands, ground-glass opacities, mosaic perfusion in early cases, and in more advanced cases, also traction bronchiectasis and honeycombing,(2,58,59) in addition to a previous clinical assessment, should be submitted to an assessment of the respiratory function, which should be thorough whenever possible (not only spirometry), with determination of DLCO. If they meet the inclusion criteria, such as absence of comorbidities that impose limitations on diagnosis and treatment procedures in the case of a cancer diagnosis, they should be followed up according to item 1.2 below.
1.2. Annual lung cancer screening is recommended to the services that meet the requirements suggested in the studies and recommendations.(27,49-52,60) Such services should plan the timely performance of tests, including reassessments in accordance with the indication of the nodules found, and the performance of procedures for diagnosis, follow-up, and treatment with the use of LD-HRCT to minimize the risks of radiation exposure.
2. Individuals aged 50 or older up to 75 years of age with occupational exposure to asbestos for one year or over or domestic and/or environmental exposure for five years or over, with 20 years’ latency or over, for any of the exposure conditions, even if they do not present asbestos-related diseases at the moment, should be considered exposed in a significant way and assessed through the use of risk calculators for inclusion in the screening program with the use of LD-HRCT of the chest. If they do not meet such criteria, they can be included in the screening program through the other factors assessed by the calculators.
3. Chest LD-HRCT screening should be performed in individuals with a history of occupational exposure to asbestos who meet the criteria described above if their lung cancer risk estimate is at least 1.5% according to Liverpool Lung Project (https://liverpoollungproject.org.uk/MLRV3/MLRCalculation.html) or CanPredict calculators.(55-57)1
4. For the assessment of CT scans in the lung cancer screening program, the classification of findings and diagnosis criteria recommended by Lung Imaging Reporting and Data System (Lung-RADS),(61) a tool recommended in lung cancer screening programs,(51,54-57) should be used.
5. All the services involved in lung cancer screening programs should have the support of smoking cessation programs.
FINAL CONSIDERATIONS The diagnosis and registration of occupational diseases have historically been inadequate and limited for many reasons, such as the deficient education of health professionals and the lack of specialized services in Brazil. Respiratory diseases deriving from asbestos exposure are included in this context. Diagnosing asbestos-related diseases is necessary to enhance the monitoring of patients’ health. Furthermore, with such a diagnosis, Brazil can have accurate knowledge of the repercussions of asbestos use, and the victims will have the right to seek compensation if they wish to, either from the State (social security, environmental care) or from the companies that generated the exposure.
The present document represents the position of the Committee on Environmental and Occupational Diseases of the Brazilian Thoracic Society on screening, diagnosis, and follow-up of asbestos-related diseases with the main objective of improving their recognition and monitoring.
AUTHOR CONTRIBUTIONS All the authors participated in one or more development stages of these recommendations, and all read and approved the final version of the manuscript.
CONFLICTS OF INTEREST None declared.
REFERENCES 1. Shukla A, Gulumian M, Hei TK, Kamp D, Rahman Q, Mossman BT. Multiple roles of oxidants in the pathogenesis of asbestos-induced diseases. Free Radic Biol Med. 2003;34(9):1117-1129. https://doi.org/10.1016/S0891-5849(03)00060-1
2. American Thoracic Society. Diagnosis and initial management of nonmalignant diseases related to asbestos. Am J Respir Crit Care Med. 2004;170(6):691-715. https://doi.org/10.1164/rccm.200310-1436ST
3. Wolff H, Vehmas T, Oksa P, Rantanen J, Vainio H. Asbestos, asbestosis, and cancer, the Helsinki criteria for diagnosis and attribution 2014: recommendations. Scand J Work Environ Health. 2015;41(1):5-15. https://doi.org/10.5271/sjweh.3462
4. GBD 2019 Risk Factors Collaborators. Global burden of 87 risk factors in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396(10258):1223-1249. https://doi.org/10.1016/S0140-6736(20)30752-2
5. Magnani C, Dalmasso P, Biggeri A, Ivaldi C, Mirabelli D, Terracini B. Increased risk of malignant mesothelioma of the pleura after residential or domestic exposure to asbestos: a case-control study in Casale Monferrato, Italy. Environ Health Perspect. 2001;109(9):915-919. https://doi.org/10.1289/ehp.01109915
6. Kwak K, Kang D, Paek D. Environmental exposure to asbestos and the risk of lung cancer: a systematic review and meta-analysis. Occup Environ Med. 2022;79(3):207-214. https://doi.org/10.1136/oemed-2020-107222
7. Algranti E, Saito CA, Carneiro AP, Moreira B, Mendonça EM, Bussacos MA. The next mesothelioma wave: mortality trends and forecast to 2030 in Brazil. Cancer Epidemiol. 2015;39(5):687-692. https://doi.org/10.1016/j.canep.2015.08.007
8. Park EK, Takahashi K, Hoshuyama T, Cheng TJ, Delgermaa V, Le GV, et al. Global magnitude of reported and unreported mesothelioma. Environ Health Perspect. 2011;119(4):514-518. https://doi.org/10.1289/ehp.1002845
9. Aberle DR, Gamsu G, Ray CS. High-resolution CT of benign asbestos-related diseases: clinical and radiographic correlation. AJR Am J Roentgenol. 1988; 151(5):883-891. https://doi.org/10.2214/ajr.151.5.883
10. Bégin R, Ostiguy G, Filion R, Colman N, Bertrand P. Computed tomography in the early detection of asbestosis. Br J Ind Med. 1993;50(8):689-698. https://doi.org/10.1136/oem.50.8.689
11. Gamsu G, Salmon CJ, Warnock ML, Blanc PD. CT quantification of interstitial fibrosis in patients with asbestosis: a comparison of two methods. AJR Am J Roentgenol. 1995;164(1):63-68. https://doi.org/10.2214/ajr.164.1.7998570
12. Gevenois PA, de Maertelaer V, Madani A, Winant C, Sergent G, De Vuyst P. Asbestosis, pleural plaques and diffuse pleural thickening: three distinct benign responses to asbestos exposure. Eur Respir J. 1998;11(5):1021-1027. https://doi.org/10.1183/09031936.98.11051021
13. Ross RM. The clinical diagnosis of asbestosis in this century requires more than a chest radiograph. Chest. 2003;124(3):1120-1128. https://doi.org/10.1378/chest.124.3.1120
14. Miao X, Yao T, Dong C, Chen Z, Wei W, Shi Z, et al. Global, regional, and national burden of non-communicable diseases attributable to occupational asbestos exposure 1990-2019 and prediction to 2035: worsening or improving? BMC Public Health. 2024; 24(1):832. https://doi.org/10.1186/s12889-024-18099-4
15. Kocarnik JM, Compton K, Dean FE, Fu W, Gaw BL, Harvey JD, et al. Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life Years for 29 Cancer Groups From 2010 to 2019: A Systematic Analysis for the Global Burden of Disease Study 2019. JAMA Oncol. 2022;8(3):420-444. https://doi.org/10.1001/jamaoncol.2021.6987
16. Algranti E, Mendonça EM, DeCapitani EM, Freitas JB, Silva HC, Bussacos MA. Non-malignant asbestos-related diseases in Brazilian asbestos-cement workers. Am J Ind Med. 2001;40(3):240-254. https://doi.org/10.1002/ajim.1095
17. Baur X. Asbestos-Related Disorders in Germany: Background, Politics, Incidence, Diagnostics and Compensation. Int J Environ Res Public Health. 2018;15(1):143. https://doi.org/10.3390/ijerph15010143
18. Sex-Specific Mortality from Asbestos-Related Diseases, Lung and Ovarian Cancer in Municipalities with High Asbestos Consumption, Brazil, 2000-2017 [published correction appears in Int J Environ Res Public Health. 2022 May 31;19(11):6720. doi: 10.3390/ijerph19116720]. Int J Environ Res Public Health. 2022;19(6):3656. https://doi.org/10.3390/ijerph19116720
19. Santana VS, Salvi L, Cavalcante F, Campos F, Algranti E. Underreporting of mesothelioma, asbestosis and pleural plaques in Brazil. Occup Med (Lond). 2021;71(4-5):223-230. https://doi.org/10.1093/occmed/kqab073
20. World Health Organization. International Agency for Research on Cancer (IARC). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Arsenic, metals, fibers and dust, Vol 100C. Lyon, France: IARC; 2012.
21. Markowitz SB, Levin SM, Miller A, Morabia A. Asbestos, asbestosis, smoking, and lung cancer. New findings from the North American insulator cohort. Am J Respir Crit Care Med. 2013;188(1):90-96. https://doi.org/10.1164/rccm.201302-0257OC
22. Malta DC, Gomes CS, Andrade FMD, Prates EJS, Alves FTA, Oliveira PPV, et al. Tobacco use, cessation, secondhand smoke and exposure to media about tobacco in Brazil: results of the National Health Survey 2013 and 2019. Rev Bras Epidemiol. 2021;24(suppl 2):e210006. https://doi.org/10.1590/1980-549720210006.supl.2
23. WHO. WHO global report on trends in prevalence of tobacco use 2000-2025. 4th ed. Geneva: World Health Organization; 2021.
24. Klebe S, Leigh J, Henderson DW, Nurminen M. Asbestos, Smoking and Lung Cancer: An Update. Int J Environ Res Public Health. 2019;17(1):258. https://doi.org/10.3390/ijerph17010258
25. gov.br. Presidência da República. Ministério do Trabalho e Emprego homepage on the Internet]. Brasília: o Ministério; c2023 [updated 2023 Feb 14; cited 2024 Apr 6]. Normas Regulamentadoras - NR. Available from: https://www.gov.br/trabalho-e-emprego/pt-br/assuntos/inspecao-do-trabalho/seguranca-e-saude-no-trabalho/ctpp-nrs/normas-regulamentadoras-nrs
26. International Labour Organization (ILO) [homepage on the Internet]. Geneva: International Labour Office; c2022 [cited 2024 Apr 6]. Guidelines for the use of the ILO International Classification of Radiographs of Pneumoconioses. Revised edition 2022. [Adobe Acrobat document, 45p.]. Available from: https://www.ilo.org/resource/ilo-international-classification-radiographs-pneumoconioses-1
27. Markowitz S, Ringen K, Dement JM, Straif K, Christine Oliver L, Algranti E, et al. Occupational lung cancer screening: A Collegium Ramazzini statement. Am J Ind Med. 2024;67(4):289-303. https://doi.org/10.1002/ajim.23572
28. Nogami S, J-P NA, Nogami M, Matsui T, Ngatu NR, Tamura T, et al. Radiographic diagnosis of Pneumoconioses by AIR Pneumo-trained physicians: Comparison with low-dose thin-slice computed tomography. J Occup Health. 2020;62(1):e12141. https://doi.org/10.1002/1348-9585.12141
29. Bégin R, Ostiguy G, Filion R, Groleau S. Recent advances in the early diagnosis of asbestosis. Semin Roentgenol. 1992;27(2):121-139. https://doi.org/10.1016/0037-198X(92)90054-6
30. Akira M, Yamamoto S, Inoue Y, Sakatani M. High-resolution CT of asbestosis and idiopathic pulmonary fibrosis. AJR Am J Roentgenol. 2003;181(1):163-169. https://doi.org/10.2214/ajr.181.1.1810163
31. Arakawa H, Kishimoto T, Ashizawa K, Kato K, Okamoto K, Honma K, et al. Asbestosis and other pulmonary fibrosis in asbestos-exposed workers: high-resolution CT features with pathological correlations. Eur Radiol. 2016;26(5):1485-1492. https://doi.org/10.1007/s00330-015-3973-z
32. Markowitz SB. Lung Cancer Screening in Asbestos-Exposed Populations. Int J Environ Res Public Health. 2022;19(5):2688. https://doi.org/10.3390/ijerph19052688
33. Miller A, Widman SA, Miller JA, Manowitz A, Markowitz SB. Comparison of x-ray films and low-dose computed tomographic scans: demonstration of asbestos-related changes in 2760 nuclear weapons workers screened for lung cancer. J Occup Environ Med. 2013;55(7):741-745. https://doi.org/10.1097/JOM.0b013e3182954067
34. Nair A, Hansell DM. High-resolution computed tomography features of smoking-related interstitial lung disease. Semin Ultrasound CT MR. 2014;35(1):59-71. https://doi.org/10.1053/j.sult.2013.10.005
35. Vehmas T, Kivisaari L, Huuskonen MS, Jaakkola MS. Scoring CT/HRCT findings among asbestos-exposed workers: effects of patient’s age, body mass index and common laboratory test results. Eur Radiol. 2005;15(2):213-219. https://doi.org/10.1007/s00330-004-2552-5
36. Raghu G, Remy-Jardin M, Myers JL, Richeldi L, Ryerson CJ, Lederer DJ, et al. Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Am J Respir Crit Care Med. 2018;198(5):e44-e68. https://doi.org/10.1164/rccm.201807-1255ST
37. Brims FJH, Kong K, Harris EJA, Sodhi-Berry N, Reid A, Murray CP, et al. Pleural Plaques and the Risk of Lung Cancer in Asbestos-exposed Subjects. Am J Respir Crit Care Med. 2020;201(1):57-62. https://doi.org/10.1164/rccm.201901-0096OC
38. Remy-Jardin M, Sobaszek A, Duhamel A, Mastora I, Zanetti C, Remy J. Asbestos-related pleuropulmonary diseases: evaluation with low-dose four-detector row spiral CT. Radiology. 2004;233(1):182-190. https://doi.org/10.1148/radiol.2331031133
39. Carrillo MC, Alturkistany S, Roberts H, Nguyen E, Chung TB, Paul N, et al. Low-dose computed tomography (LDCT) in workers previously exposed to asbestos: detection of parenchymal lung disease. J Comput Assist Tomogr. 2013;37(4):626-630. https://doi.org/10.1097/RCT.0b013e31828e1b8e
40. Harris EJA, Lim KP, Moodley Y, Adler B, Sodhi-Berry N, Reid A, et al. Low dose CT detected interstitial lung abnormalities in a population with low asbestos exposure. Am J Ind Med. 2021;64(7):567-575. https://doi.org/10.1002/ajim.23251
41. Zhu X, Yu J, Huang Z. Low-dose chest CT: optimizing radiation protection for patients. AJR Am J Roentgenol. 2004;183(3):809-816. https://doi.org/10.2214/ajr.183.3.1830809
42. Ludes C, Schaal M, Labani A, Jeung MY, Roy C, Ohana M. Ultra-low dose chest CT: The end of chest radiograph? [Article in French]. Presse Med. 2016;45(3):291-301. https://doi.org/10.1016/j.lpm.2015.12.003
43. Neroladaki A, Botsikas D, Boudabbous S, Becker CD, Montet X. Computed tomography of the chest with model-based iterative reconstruction using a radiation exposure similar to chest X-ray examination: preliminary observations. Eur Radiol. 2013;23(2):360-366. https://doi.org/10.1007/s00330-012-2627-7
44. O’Brien C, Kok HK, Kelly B, Kumamaru K, Sahadevan A, Lane S, et al. To investigate dose reduction and comparability of standard dose CT vs Ultra low dose CT in evaluating pulmonary emphysema. Clin Imaging. 2019;53:115-119. https://doi.org/10.1016/j.clinimag.2018.10.012
45. Markowitz SB, Manowitz A, Miller JA, Frederick JS, Onyekelu-Eze AC, Widman SA, et al. Yield of Low-Dose Computerized Tomography Screening for Lung Cancer in High-Risk Workers: The Case of 7189 US Nuclear Weapons Workers. Am J Public Health. 2018;108(10):1296-1302. https://doi.org/10.2105/AJPH.2018.304518
46. Radiological Society of North America (RSNA) [homepage on the Internet]. Oakbrook, IL: RSNA; c2022 [updated 2022 Nov 1; cited 2024 Apr 25]. Effective radiation dose in adults Available from: https://wwwradiologyinfoorg/en/info/safety-xray
47. Brenner DJ. Radiation risks potentially associated with low-dose CT screening of adult smokers for lung cancer. Radiology. 2004;231(2):440-445. https://doi.org/10.1148/radiol.2312030880
48. Jonas DE, Reuland DS, Reddy SM, Nagle M, Clark SD, Weber RP, et al. Screening for Lung Cancer With Low-Dose Computed Tomography: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force. JAMA. 2021;325(10):971-987. https://doi.org/10.1001/jama.2021.0377
49. U.S. Preventive Services Task Force (USPSTF) [homepage on the Internet]. Rockville, MD: USPSTF; c2021 [updated 2021 Mar 9; cited 2024 Apr 1]. Final Recommendation Statement. Lung Cancer: Screening. Available from: https://www.uspreventiveservicestaskforce.org/uspstf/document/RecommendationStatementFinal/lung-cancer-screening
50. Wolf AMD, Oeffinger KC, Shih TY-C, Walter LC, Church TR, Fontham ETH, et al. Screening for lung cancer: 2023 guideline update from the American Cancer Society. CA Cancer J Clin. 2024;74(1):50-81. https://doi.org/10.3322/caac.21811
51. Baldwin D, O’Dowd E, Tietzova I, Kerpel-Fronius A, Heuvelmans M, Snoeckx A, et al. Developing a pan-European technical standard for a comprehensive high-quality lung cancer computed tomography screening programme: an ERS technical standard. European Respiratory Journal. 2023;61(6):2300128. https://doi.org/10.1183/13993003.00128-2023
52. Pereira LFF, Santos RSD, Bonomi DO, Franceschini J, Santoro IL, Miotto A, et al. Lung cancer screening in Brazil: recommendations from the Brazilian Society of Thoracic Surgery, Brazilian Thoracic Association, and Brazilian College of Radiology and Diagnostic Imaging. J Bras Pneumol. 2024;50(1):e20230233. https://doi.org/10.36416/1806-3756/e20230233
53. National Lung Screening Trial Research Team; Aberle DR, Adams AM, Berg CD, Black WC, Clapp JD, et al. Reduced lung-cancer mortality with low-dose computed tomographic screening. N Engl J Med. 2011;365(5):395-409. https://doi.org/10.1056/NEJMoa1102873
54. de Koning HJ, van der Aalst CM, de Jong PA, Scholten ET, Nackaerts K, Heuvelmans MA, et al. Reduced Lung-Cancer Mortality with Volume CT Screening in a Randomized Trial. N Engl J Med. 2020;382(6):503-513. https://doi.org/10.1056/NEJMoa1911793
55. Cassidy A, Myles JP, van Tongeren M, et al. The LLP risk model: an individual risk prediction model for lung cancer. Br J Cancer. 2008;98(2):270-276. https://doi.org/10.1038/sj.bjc.6604158
56. Field JK, Vulkan D, Davies MPA, Duffy SW, Gabe R. Liverpool Lung Project lung cancer risk stratification model: calibration and prospective validation. Thorax. 2021;76(2):161-168. https://doi.org/10.1136/thoraxjnl-2020-215158
57. Liao W, Coupland CAC, Burchardt J, Baldwin DR; DART initiative; Gleeson FV, et al. Predicting the future risk of lung cancer: development, and internal and external validation of the CanPredict (lung) model in 19•67 million people and evaluation of model performance against seven other risk prediction models. Lancet Respir Med. 2023;11(8):685-697. https://doi.org/10.1016/S2213-2600(23)00050-4
58. Akira M, Morinaga K. The comparison of high-resolution computed tomography findings in asbestosis and idiopathic pulmonary fibrosis. Am J Ind Med. 2016;59(4):301-306. https://doi.org/10.1002/ajim.22573
59. Masanori A. Imaging diagnosis of classical and new pneumoconiosis: predominant reticular HRCT pattern. Insights Imaging. 2021;12(1):33. https://doi.org/10.1186/s13244-021-00966-y
60. Mazzone PJ, Silvestri GA, Souter LH, Caverly TJ, Kanne JP, Katki HA, et al. Screening for Lung Cancer: CHEST Guideline and Expert Panel Report. Chest. 2021;160(5):e427-e494. https://doi.org/10.1016/j.chest.2021.06.063
61. American College of Radiology (ACR) [homepage on the Internet]. Philadelphia, PA: ACR; c2022 [cited 2024 Apr 1]. Lung-RADS® v2022. [Adobe Acrobat document, 2p.]. Available from: https://www.acr.org/-/media/ACR/Files/RADS/Lung-RADS/Lung-RADS-2022.pdf