Role of Occupation in Shaping Cancer Disparities
Abstract
:Simple Summary
Abstract
1. Introduction
2. Cancer Screening by Income, Health Insurance and Occupation
3. The Mediating Role of Occupation in the Association between Race/Ethnicity and Education and Cancer Risk
3.1. Racial and Ethnic Minorities
3.2. Educational Level
3.3. An Example of Mediation Analysis: Education, Occupational Carcinogens and Lung Cancer Risk
4. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
- Bogovski, P. Historical perspectives of occupational cancer. J. Toxicol. Environ. Health Part A 1980, 6, 921–939. [Google Scholar] [CrossRef] [PubMed]
- Kennaway, E.L.; Kennaway, N.M. The social distribution of cancer of the scrotum and cancer of the penis. Cancer Res. 1946, 6, 49–53. [Google Scholar]
- Costello, J. Morbidity and mortality study of shale oil workers in the United States. Environ Health Perspect. 1979, 30, 205–208. [Google Scholar] [CrossRef]
- Nabavizadeh, B.; Amend, G.M.; Breyer, B.N. Workers Died of Dyes: The Discovery of Occupational Bladder Cancers. Urology 2021, 154, 4–7. [Google Scholar] [CrossRef] [PubMed]
- Boffetta, P.; Malvezzi, M.; Pira, E.; Negri, E.; La Vecchia, C. International Analysis of Age-Specific Mortality Rates From Mesothelioma on the Basis of the International Classification of Diseases, 10th Revision. J. Glob. Oncol. 2018, 4, 1–15. [Google Scholar] [CrossRef] [PubMed]
- Havet, N.; Penot, A.; Morelle, M.; Perrier, L.; Charbotel, B.; Fervers, B. Trends in occupational disparities for exposure to carcinogenic, mutagenic and reprotoxic chemicals in France 2003–10. Eur. J. Public Health 2017, 27, 425–432. [Google Scholar] [CrossRef] [PubMed]
- Hrubá, F.; Fabiáová, E.; Bencko, V.; Cassidy, A.; Lissowska, J.; Mates, D.; Rudnai, P.; Zaridze, D.; Foretová, L.; Janout, V.; et al. Socioeconomic indicators and risk of lung cancer in Central and Eastern Europe. Cent. Eur. J. Public Health 2009, 17, 115–121. [Google Scholar] [CrossRef]
- Pearce, N.; Susser, M.; Boffetta, P. Social Inequalities and Cancer; IARC: Lyon, France, 1997; pp. 1–15. [Google Scholar]
- Available online: https://www.careerprofiles.info/occupations-by-education-level.html (accessed on 2 July 2022).
- Colon-Otero, G.; Smallridge, R.C.; Solberg, L.A., Jr.; Keith, T.D.; Woodward, T.A.; Willis, F.B.; Dunn, A.N. Disparities in participation in cancer clinical trials in the United States: A symptom of a healthcare system in crisis. Cancer 2008, 112, 447–454. [Google Scholar] [CrossRef]
- Rajaguru, V.; Kim, T.H.; Shin, J.; Lee, S.G. Income Disparities in Cancer Screening: A Cross-Sectional Study of the Korean National Health and Nutrition Examination Survey, 2013–2019. Front. Public Health 2022, 10, 820643. [Google Scholar] [CrossRef]
- Leinonen, M.K.; Campbell, S.; Klungsøyr, O.; Lönnberg, S.; Hansen, B.T.; Nygård, M. Personal and provider level factors influence participa-tion to cervical cancer screening: A retrospective register-based study of 1.3 million women in Norway. Prev. Med. 2017, 94, 31–39. [Google Scholar] [CrossRef]
- Broberg, G.; Wang, J.; Östberg, A.L.; Adolfsson, A.; Nemes, S.; Sparén, P.; Strander, B. Socio-economic and demographic determinants af-fecting participation in the Swedish cervical screening program: A population-based case-control study. PLoS ONE 2018, 13, e0190171. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Shim, H.-Y.; Jun, J.K.; Shin, J.-Y. Employment conditions and use of gastric cancer screening services in Korea: A nationwide survey. BMC Public Health 2019, 19, 485. [Google Scholar] [CrossRef]
- Shete, S.; Deng, Y.; Shannon, J.; Faseru, B.; Middleton, D.; Iachan, R.; Bernardo, B.; Balkrishnan, R.; Kim, S.J.; Huang, B.; et al. Differences in Breast and Colorectal Cancer Screening Adherence Among Women Residing in Urban and Rural Communities in the United States. JAMA Netw. Open 2021, 4, e2128000. [Google Scholar] [CrossRef] [PubMed]
- Fedewa, S.A.; Sauer, A.G.; DeSantis, C.; Siegel, R.L.; Jemal, A. Disparities in cancer screening by occupational characteristics. Prev. Med. 2017, 105, 311–318. [Google Scholar] [CrossRef]
- Carney, P.A.; O’Malley, J.; Buckley, D.I.; Mori, M.; Lieberman, D.A.; Fagnan, L.J.; Wallace, J.; Liu, B.; Morris, C. Influence of health insurance coverage on breast, cervical, and colorectal cancer screening in rural primary care settings. Cancer 2012, 118, 6217–6225. [Google Scholar] [CrossRef] [PubMed]
- Ishii, K.; Tabuchi, T.; Iso, H. Combined patterns of participation in cervical, breast, and colorectal cancer screenings and factors for non-participation in each screening among women in Japan. Prev. Med. 2021, 150, 106627. [Google Scholar] [CrossRef] [PubMed]
- Tapera, O.; Kadzatsa, W.; Nyakabau, A.M.; Mavhu, W.; Dreyer, G.; Stray-Pedersen, B.; Sjh, H. Sociodemographic inequities in cervical cancer screening, treatment and care amongst women aged at least 25 years: Evidence from surveys in Harare, Zimbabwe. BMC Public Health 2019, 19, 428. [Google Scholar] [CrossRef]
- Amin, R.; Kolahi, A.A.; Jahanmehr, N.; Abadi, A.R.; Sohrabi, M.R. Disparities in cervical cancer screening participation in Iran: A cross-sectional analysis of the 2016 nationwide STEPS survey. BMC Public Health 2020, 20, 1594. [Google Scholar] [CrossRef] [PubMed]
- Naik, B.N.; Chandrika, K.; Kanungo, S. Awareness on cancer cervix, willingness, and barriers for screening of cancer cervix among women: A community-based cross-sectional study from urban Pondicherry. Indian J. Public Health 2020, 64, 374–380. [Google Scholar] [CrossRef]
- Moser, K.; Patnick, J.; Beral, V. Inequalities in reported use of breast and cervical screening in Great Britain: Analysis of cross sectional survey data. BMJ 2009, 338, b2025. [Google Scholar] [CrossRef]
- Getachew, S.; Getachew, E.; Gizaw, M.; Ayele, W.; Addissie, A.; Kantelhardt, E.J. Cervical cancer screening knowledge and barriers among women in Addis Ababa, Ethiopia. PLoS ONE 2019, 14, e0216522. [Google Scholar] [CrossRef] [PubMed]
- Asgary, R. Cancer screening in the homeless population. Lancet Oncol. 2018, 19, e344–e350. [Google Scholar] [CrossRef]
- Baggett, T.P.; Chang, Y.; Porneala, B.C.; Bharel, M.; Singer, D.E.; Rigotti, N.A. Disparities in Cancer Incidence, Stage, and Mortality at Boston Health Care for the Homeless Program. Am. J. Prev. Med. 2015, 49, 694–702. [Google Scholar] [CrossRef] [PubMed]
- Asgary, R.; Sckell, B.; Alcabes, A.; Naderi, R.; Ogedegbe, G. Perspectives of cancer and cancer screening among homeless adults of New York City shelter-based clinics: A qualitative approach. Cancer Causes Control 2015, 26, 1429–1438. [Google Scholar] [CrossRef]
- Kilic, S.S.; Mayo, Z.S.; Weleff, J.; Strzalka, C.; Hall, E.F.; Obi, E.E.; Anderson, N.; Phelan, M.P.; Cherian, S.S.; Tendulkar, R.D.; et al. Breast cancer screening in persons experiencing homelessness. J. Clin. Oncol. 2022, 40, 6515. [Google Scholar] [CrossRef]
- Williams, L.B.; McCall, A.; Looney, S.W.; Joshua, T.; Tingen, M.S. Demographic, psychosocial, and behavioral associations with cancer screening among a homeless population. Public Health Nurs. 2018, 35, 281–290. [Google Scholar] [CrossRef]
- Chau, S.; Chin, M.; Chang, J.; Luecha, A.; Cheng, E.; Schlesinger, J.; Rao, V.; Huang, D.; Maxwell, A.E.; Usatine, R.; et al. Cancer risk behaviors and screening rates among homeless adults in Los Angeles County. Cancer Epidemiol. Biomark. Prev. 2002, 11, 431–438. [Google Scholar]
- Kullgren, J.T.; Dicks, T.N.; Fu, X.; Richardson, D.; Tzanis, G.L.; Tobi, M.; Marcus, S.C. Financial incentives for completion of fecal occult blood tests among veterans: A 2-stage, pragmatic, cluster, randomized, controlled trial. Ann. Intern. Med. 2014, 161, S35–S43. [Google Scholar] [CrossRef]
- O’Keefe, L.C.; Sullivan, M.M.; McPhail, A.; van Buren, K.; Dewberry, N. Screening for Colorectal Cancer at the Worksite. Work. Health Saf. 2018, 66, 183–190. [Google Scholar] [CrossRef]
- Mizuno, S.; Miki, I.; Ishida, T.; Yoshida, M.; Onoyama, M.; Azuma, T.; Habu, Y.; Inokuchi, H.; Ozasa, K.; Miki, K.; et al. Prescreening of a High-Risk Group for Gastric Cancer by Serologically Determined Helicobacter pylori Infection and Atrophic Gastritis. Am. J. Dig. Dis. 2010, 55, 3132–3137. [Google Scholar] [CrossRef]
- Pukkala, E.; Martinsen, J.I.; Lynge, E.; Gunnarsdottir, H.K.; Sparén, P.; Tryggvadottir, L.; Weiderpass, E.; Kjaerheim, K. Occupation and cancer—Follow-up of 15 million people in five Nordic countries. Acta Oncol. 2009, 48, 646–790. [Google Scholar] [CrossRef] [PubMed]
- Li, W.-Q.; Cho, E.; Wu, S.; Li, S.; Matthews, N.H.; Qureshi, A.A. Host Characteristics and Risk of Incident Melanoma by Breslow Thickness. Cancer Epidemiol. Biomark. Prev. 2019, 28, 217–224. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bevers, T.B.; Helvie, M.; Bonaccio, E.; Calhoun, K.E.; Daly, M.B.; Farrar, W.B.; Garber, J.E.; Gray, R.; Greenberg, C.C.; Greenup, R.; et al. Breast Cancer Screening and Diagnosis, Version 3.2018, NCCN Clinical Practice Guidelines in Oncology. J. Natl. Compr. Canc. Netw. 2018, 16, 1362–1389. [Google Scholar] [CrossRef] [PubMed]
- US Preventive Services Task Force; Curry, S.J.; Krist, A.H.; Owens, D.K.; Barry, M.J.; Caughey, A.B.; Davidson, K.W.; Doubeni, C.A.; Epling, J.W., Jr.; Kemper, A.R.; et al. Screening for Cervical Cancer: US Preventive Services Task Force Recommendation Statement. JAMA 2018, 320, 674–686. [Google Scholar] [CrossRef]
- Ma, G.X.; Yin, L.; Gao, W.; Tan, Y.; Liu, R.; Fang, C.; Ma, X.S. Workplace-Based Breast Cancer Screening Intervention in China. Cancer Epidemiol. Biomarkers Prev. 2012, 21, 358–367. [Google Scholar] [CrossRef] [PubMed]
- Behnke, A.-L.; Krings, A.; Wormenor, C.M.; Dunyo, P.; Kaufmann, A.M.; Amuah, J.E. Female health-care providers’ advocacy of self-sampling after participating in a workplace program for cervical cancer screening in Ghana: A mixed-methods study. Glob. Health Action 2020, 13, 1838240. [Google Scholar] [CrossRef]
- Hart, A.R.; Glover, N.; Howick-Baker, J.; Mayberry, J.F. An industry based approach to colorectal cancer screening in an asymptomatic population. Postgrad. Med. J. 2003, 79, 646–649. [Google Scholar] [CrossRef]
- Warner, E.L.; Martel, L.; Ou, J.Y.; Nam, G.E.; Carbajal-Salisbury, S.; Fuentes, V.; Kirchhoff, A.C.; Kepka, D. A Workplace-Based Intervention to Improve Awareness, Knowledge, and Utilization of Breast, Cervical, and Colorectal Cancer Screenings Among Latino Service and Manual Labor Employees in Utah. J. Community Health 2019, 44, 256–264. [Google Scholar] [CrossRef]
- Schill, A.L.; Chosewood, L.C. The NIOSH Total Worker Health™ program: An overview. J. Occup. Environ. Med. 2013, 55, S8–S11. [Google Scholar] [CrossRef]
- Lee, H.-E.; Zaitsu, M.; Kim, E.-A.; Kawachi, I. Cancer Incidence by Occupation in Korea: Longitudinal Analysis of a Nationwide Cohort. Saf. Healtjh Work 2020, 11, 41–49. [Google Scholar] [CrossRef]
- Michaels, D. Occupational cancer in the black population: The health effects of job discrimination. J. Natl. Med Assoc. 1983, 75, 1014–1018. [Google Scholar] [PubMed]
- Juon, H.-S.; Hong, A.; Pimpinelli, M.; Rojulpote, M.; McIntire, R.; Barta, J.A. Racial disparities in occupational risks and lung cancer incidence: Analysis of the National Lung Screening Trial. Prev. Med. 2021, 143, 106355. [Google Scholar] [CrossRef] [PubMed]
- Boyle, T.; Carey, R.N.; Peters, S.; Glass, D.C.; Fritschi, L.; Reid, A. Demographic and Occupational Differences Between Ethnic Minority Workers Who Did and Did Not Complete the Telephone Survey in English. Ann. Occup. Hyg. 2015, 59, 862–871. [Google Scholar] [CrossRef] [PubMed]
- Carey, R.N.; El-Zaemey, S.; Daly, A.; Fritschi, L.; Glass, D.C.; Reid, A. Are There Ethnic Disparities in Exposure to Workplace Hazards Among New Zealand Migrants to Australia? Asia Pac. J. Public Health 2021, 33, 870–879. [Google Scholar] [CrossRef]
- Gosselin, A.; Daly, A.; El Zaemey, S.; Fritschi, L.; Glass, D.; Perez, E.R.; Reid, A. Does exposure to workplace hazards cluster by occupational or sociodemographic characteristics? An analysis of foreign-born workers in Australia. Am. J. Ind. Med. 2020, 63, 803–816. [Google Scholar] [CrossRef]
- Pokhrel, A.; Martikainen, P.; Pukkala, E.; Rautalahti, M.; Seppä, K.; Hakulinen, T. Education, survival and avoidable deaths in cancer pa-tients in Finland. Br. J. Cancer 2010, 103, 1109–1114. [Google Scholar] [CrossRef]
- Menvielle, G.; Boshuizen, H.; Kunst, A.E.; Vineis, P.; Dalton, S.O.; Bergmann, M.M.; Hermann, S.; Veglia, F.; Ferrari, P.; Overvad, K.; et al. Occupational exposures contribute to educational inequalities in lung cancer incidence among men: Evidence from the EPIC prospective cohort study. Int. J. Cancer 2010, 126, 1928–1935. [Google Scholar] [CrossRef]
- Lortet-Tieulent, J.; Georges, D.; Bray, F.; Vaccarella, S. Profiling global cancer incidence and mortality by socioeconomic development. Int. J. Cancer 2020, 147, 3029–3036. [Google Scholar] [CrossRef]
- Coughlin, S.S. Social determinants of colorectal cancer risk, stage, and survival: A systematic review. Int. J. Color. Dis. 2020, 35, 985–995. [Google Scholar] [CrossRef]
- Coughlin, S.S. Social determinants of breast cancer risk, stage, and survival. Breast Cancer Res. Treat. 2019, 177, 537–548. [Google Scholar] [CrossRef]
- Albano, J.D.; Ward, E.; Jemal, A.; Anderson, R.; Cokkinides, V.E.; Murray, T.; Henley, S.J.; Liff, J.; Thun, M.J. Cancer Mortality in the United States by Education Level and Race. JNCI J. Natl. Cancer Inst. 2007, 99, 1384–1394. [Google Scholar] [CrossRef] [PubMed]
- Bardin-Mikolajczak, A.; Lissowska, J.; Zaridze, D.; Szeszenia-Dabrowska, N.; Rudnai, P.; Fabianova, E.; Mates, D.; Navratilova, M.; Bencko, V.; Janout, V.; et al. Occupation and risk of lung cancer in Central and Eastern Eu-rope: The IARC multi-center case-control study. Cancer Causes Control 2007, 18, 645–654. [Google Scholar] [CrossRef] [PubMed]
- Vanderweele, T.J.; Vansteelandt, S. Conceptual issues concerning mediation, interventions and composition. Stat. Interface 2009, 2, 457–468. [Google Scholar] [CrossRef]
- Emsley, R.; Liu, H. PARAMED: Stata Module to Perform Causal Mediation Analysis Using Parametric Regression Models. Statistical Software Components; Boston College Department of Economics: Boston, MA, USA, 2013. [Google Scholar]
- StataCorp. Stata Statistical Software: Release; StataCorp LLC: College Station, TX, USA, 2019. [Google Scholar]
- GBD. 2016 Occupational Carcinogens Collaborators. Occup. Environ. Med. 2020, 77, 151–159. [Google Scholar]
- Mata, M.S.; Costa, Í.D.C.C. Composition of the Health Inequality Index analyzed from the inequalities in mortality and socioeconomic conditions in a Brazilian state capital. Cien. Saude Colet. 2020, 25, 1629–1640. [Google Scholar] [CrossRef] [PubMed]
Study | Country | Disparity Factors | Population | Findings | |||
---|---|---|---|---|---|---|---|
Rajaguru et al., 2022 [11] | Korea | Education Employment Insurance Income | 20,347, both sexes, aged 40 and older targeted for cancer screening; Korea National Health and Nutrition Examination Survey (KNHANES) | Use of cancer screening | |||
University or over vs. elementary: 1.25, 1.02–1.47 | |||||||
Occupation vs. no occupation: 1.41, 1.15–1.73 | |||||||
Private vs. no private health insurance: 2.73, 1.50–4.94 | |||||||
Income Q4: 4.07, 1.63–10.13 (reference: Q1) | |||||||
Leinonen et al., 2017 [12] | Norway | Education Occupation Employment Income | Norwegian women targeted for cervical cancer screening | Percentages of non-adherence: | |||
42% from primary school, 30% from university; | |||||||
41% manual, trades, military occupation, 28% managerial occupation; | |||||||
43% unemployed, 30% employed; | |||||||
45% lowest income, 29% highest income | |||||||
Broberg G et al., 2018 [13] | Sweden | Income Education Employment | Women aged 30–60 targeted for cervical cancer screening. 314,302 cases (no smear for 6–8 years); 266,706 controls (smear within 90 days) | Predictors of non-adherence: | |||
Disposable family income (<24.222 € vs. >50.111 €): 2.06, 2.01–2.11; | |||||||
Low education: (≤9 years vs. ≥12 years) 1.77, 1.73–1.81; | |||||||
Unemployment: 2.15, 2.11–2.19 | |||||||
Shim HY et al., 2019 [14] | Korea | Occupation Working hours Shifts | 5626, both sexes, aged 40 and over targeted for gastric cancer screening | Prediction of participation to screening: | |||
Manual workers: 0.74, 0.55–0.99 | |||||||
Sales/service workers: 0.62, 0.47–0.81 | |||||||
Machine operators: 0.67, 0.50–0.91 | |||||||
vs office workers/clerk; | |||||||
Part-time workers: 0.81, 0.67–0.99 vs. full-time workers; | |||||||
≥60 working hours: 0.93, 0.78–1.11 vs. ≤40 h; | |||||||
Shift workers: 0.87, 0.73–1.04 vs. day workers (adjusted for age, gender, smoking and alcohol) | |||||||
Shete S et al., 2021 [15] | USA (pooled analysis from 11 population-based surveys) | Insurance Education | 2897 women aged 50–75 targeted for colorectal and breast cancer screening | Difference in cancer screening participation among US women | |||
No difference by income in CCR and BC screening | |||||||
CCR participation 82% in urban vs. 78% in rural residents, no difference in breast | |||||||
CCR screening participation: | |||||||
Private or employee-based health insurance: 1.99, 1.30–3.06 vs. no insurance | |||||||
Medicare: 2.34, 1.43–3.84 vs. no insurance | |||||||
Medicaid: 2.00, 1.15–3.49 vs. no insurance | |||||||
Education ≥ college: 1.30, 0.99–1.71 | |||||||
vs. ≤high school | |||||||
Post-high school trainings: 1.15, 0.88–1.51 vs. ≤high school | |||||||
BC screening participation: | |||||||
Private or employee-based health insurance: 3.80, 2.45–5.88 vs. no insurance | |||||||
Medicare: 2.84, 1.81–4.47 vs. no insurance | |||||||
Medicaid: 2.58, 1.47–4.52 vs. no insurance | |||||||
Education ≥ college: 1.19, 0.90–1.58 vs. ≤ high school | |||||||
Post-high school trainings: 1.17, 0.90–1.52 vs. ≤ high school | |||||||
Fedewa et al., 2017 [16] | USA | Occupational characteristics (occupation, industry type and employer size) | National Health Interview Surveys (NHIS) among eligible US workers (CC women 21–65 years; n = 20,997), (BC women ≥ 40 years; n = 14,258) and (CRC men and women ≥ 50 years; n = 17,333) | Higher rates of colonoscopy in larger employers (500+ workers), | |||
lower rates in smaller size employers (1–24 workers) | |||||||
Insured employees % positively related to employer size | |||||||
Participation to CC screening: | |||||||
<50% in construction, food service, | |||||||
production/transport, healthcare/personal support workers; | |||||||
66% in scientists and educators | |||||||
Higher % of uninsured in construction | |||||||
and production/transport workers (also with lower adherence to cancer screening). | |||||||
(Ref =Healthcare practitioners) | |||||||
Food service | 0.94 | 0.9 | 0.98 | ||||
Construction | 0.91 | 0.87 | 0.95 | ||||
Sales | 0.94 | 0.9 | 0.97 | ||||
Office support | 0.97 | 0.95 | 1 | ||||
Production | 0.95 | 0.91 | 0.98 | ||||
Carney et al., 2012 [17] | USA | Insurance | Oregon Rural Practice-based Research Network (ORPRN) | Up-to-date BC screening status clinical breast examination: | |||
Medicare/Medicare plus private: 1.63, 1.04–2.56 | |||||||
Medicaid/Medicaid plus private: 0.98, 0.41–2.31 | |||||||
Uninsured: 0.76, 0.39–1.48 | |||||||
Mammography: | |||||||
Medicare/Medicare plus private: 0.73 (0.53–1.02) | |||||||
Medicaid/Medicaid plus private: 0.67 (0.41–1.09) | |||||||
Uninsured:0.44 (0.24–0.79) | |||||||
CC screening | |||||||
Medicare/Medicare plus private: 0.62 (0.25–1.55) | |||||||
Medicaid/Medicaid plus private: 0.79 (0.24–2.58) | |||||||
Uninsured: 0.48 (0.19–1.24) | |||||||
CCR screening | |||||||
Medicare/Medicare plus private: 0.77 (0.53–1.10) | |||||||
Medicaid/Medicaid plus private: 0.60 (0.34–1.05) | |||||||
Uninsured:0.43 (0.19–1.00) | |||||||
Ishii et al., 2021 [18] | Japan | Education Employment status | 2016 Comprehensive Survey of Living Conditions of People on Health and Welfare, a national cross-sectional survey conducted by the Japanese Ministry of Health, Labor and Welfare. Japanese women targeted for CC, BC and CRC screening 115,254 aged 40–69 | Participation to CC, BC and CRC screening: | |||
Educational attainment | CC | BC | CRC | ||||
University | 54.6 | 56.1 | 46.3 | ||||
College/vocational school | 48.3 | 48.4 | 41.7 | ||||
High school | 42.4 | 43.9 | 39.6 | ||||
Junior high school | 28.4 | 29.5 | 30.5 | ||||
Employment status | |||||||
Permanent worker | 58.7 | 59.9 | 53.9 | ||||
Contracted worker | 53.6 | 55.1 | 50.2 | ||||
Dispatched worker | 46.3 | 46.9 | 34.1 | ||||
Part-time worker | 44.3 | 44.9 | 37.1 | ||||
Self-employed/other | 42.6 | 43.6 | 37.6 | ||||
Homemaker | 39.7 | 41.4 | 36.5 | ||||
Not working | 29.5 | 32 | 31.6 | ||||
Tapera et al., 2019 [19] | Zimbabwe | Education Occupation Personal income Household income Wealth quintile | 143 women aged 25 and older targeted for cervical cancer screening | Education | |||
Primary | 0.22 | to 895 | |||||
Secondary | 2.14 | 0.23 to 19.82 | |||||
Higher | – | – | |||||
None | |||||||
Occupation | |||||||
Unemployed | 0.1 | 0.01 to 1.60 | |||||
Professional | 0.84 | 0.05 to 13.11 | |||||
Self-employed | Ref | – | |||||
Other | 0.67 | 0.02 to 22.98 | |||||
Amin et al., 2020 [20] | Iran | Education Employment status Insurance | Education | ||||
Illiterate | 1 | ||||||
1–6 years | 1.76 | 1.531 | 2.029 | ||||
6–12 years | 2.47 | 2.088 | 2.932 | ||||
>12 years | 2.24 | 1.803 | 2.786 | ||||
Employment status | |||||||
Unemployed | 1 | ||||||
Employed | 0.83 | 0.714 | 0.986 | ||||
Retired | 1.07 | 0.713 | 1.622 | ||||
Student | 0.92 | 0.423 | 2.019 | ||||
Insurance | |||||||
No | 1 | ||||||
Yes | 1.5 | 1.245 | 1.808 |
Ref. | Outcome | Type of Cancer | Population | Industry/Type of Exposure | Data | Finding |
---|---|---|---|---|---|---|
Michaels D, 1983 [43] | Mortality | Lung | Black | Steel workers | 89% of Blacks working in coke plants were employed in ovens vs. 31% of Whites | Three times higher lung cancer mortality in Blacks than in Whites employed in the same coke plants. |
Incidence | Stomach, lung, blood, bladder, lymphatic and prostate | Black | Rubber industry | 27% of Blacks working on mixing and compounding vs. 3% of Whites | Elevated risk of stomach, lung, blood, bladder, lymphatic and prostate cancer in mixing and compounding workers. Two times higher rates of lung and prostate cancer in Blacks than in Whites working in the same area. | |
Mortality | Shipyards | 38% of the shipyard workforce at the end of World War II were Black | High mortality for asbestos-related cancers. | |||
Incidence | Lung | Black | Foundry | More than 25% of foundry workers were Black at the end of World War II | Black foundry workers are at a greater risk than the industry’s White workers. | |
Juon HS et al., 2021 [44] | Cancer incidence; prevalence of exposure to carcinogens of the lung | Lung | Black | NA | Black vs. White Lung cancer incidence: 4.3% vs. 3.9%; OR=1.24, 1.01–1.53 (adjusted for smoking and pack-years) Overall exposure prevalence: 32% vs. 28%
Similar stage at diagnosis. | Blacks seem to need a particular protection and need to be addressed with educational programs at the workplace. |
Boyle et al., 2015 [45] | Occupational exposure | NA | Ethnic minorities in Australia | NA | Marked difference in the exposure to the overall carcinogens (p < 0.001), particularly high among Arabic people not speaking English. Higher solar radiation and diesel exhaust in Arabic; higher environmental tobacco smoke in Chinese; higher polycyclic aromatic hydrocarbons in the Vietnamese population. | Targeted and informed occupational health and safety measures to be implemented based on the different prevalence of exposure to occupational carcinogens by ethnic groups. |
Carey RN et al., 2021 [46] | Occupational exposure | NA | Ethnic minorities in Australia | Exposure to benzene, diesel engine exhaust, environmental tobacco smoke, ionizing radiation, lead, polycyclic aromatic hydrocarbons other than vehicle exhausts, graveyard shiftwork, silica, solar ultraviolet radiation and wood dust | 79% of Māori/Pasifika workers vs. 67% of New Zealand Caucasian workers were exposed to at least one occupational carcinogen. | Ethnic disparities in occupational exposure to carcinogens after migration to Australia. Māori/Pasifika workers were more likely to report exposure to carcinogens, in particular environmental tobacco smoke. |
Gosselin A et al., 2020 [47] | Occupational exposure | NA | Australian immigrants born in New Zealand, India and Philippines | Exposure to solar and artificial ultraviolet radiation, diesel engine exhaust, environmental tobacco smoke, benzene, lead, silica, wood dust, other polycyclic aromatic hydrocarbons and shift work | Risk of exposure to at least one occupational carcinogen in New Zealand workers compared to Indian: 1.61, 1.12–2.32. Diesel exhaust exposure in New Zealand workers compared to Indian: 2.61, 1.60–4.25. | The prevalence of exposure to workplace hazards varied by both social position and occupational characteristics. Disparities in exposure to some workplace hazards occurred among this population as a result of their social position and irrespective of the type of job they undertook. The most vulnerable groups for exposure to carcinogens were young workers who worked long hours in smaller companies, particularly if they were born in New Zealand. Examining occupational characteristics alone may hide discrepancies related to exposure to carcinogens among workers. Subgroups of workers may have a particularly high exposure to carcinogens. |
Pokhrel A et al., 2010 [48] | Cancer survival | NA | Finland | NA | In 1996–2005, 4–7% of the deaths in Finnish cancer patients could have been avoided in the 5 years after diagnosis, if all the patients had the highest educational background. | High survival rates in highly educated and highly health-conscious people; low survival rates in those with low education; less favorable distribution of tumor stages in the lower education category. In 1996–2005, 8–11% of first 5-year cancer deaths would have been avoided if all the patients had the same cancer and the mortality for other causes had been the same as that in the highest educational category. |
Menvielle G et al., 2010 [49] | Occupational exposure | Lung | Men, EPIC cohort (Denmark, the United Kingdom, Germany, Italy, Spain and Greece) | Exposure to asbestos, heavy metals and polycyclic aromatic hydrocarbons | After adjustment (smoke and fruits/vegetables), occupation explained 14% of the excess risk. Relative incidence of inequalities: 1.75 (1.27–2.41) after adjusting for tobacco smoking, fruit and vegetable consumption. | A common hypothesis is that a higher exposure to risk factors explains the higher incidence of lung cancer in low socioeconomic groups. The risk factors are seen as intermediate variables or mediators between education and the onset of lung cancer. Birth cohort analyses suggest an effect of occupational exposures among older men but not younger men on educational inequalities. |
Characteristics | Lung Cancer Cases | Controls | OR, 95% CI |
---|---|---|---|
Smoking status | |||
-Never | 274 (9.6%) | 1038 (35.4%) | Ref |
-Former | 1310 (45.8%) | 995 (33.9%) | 6.27, 5.27–7.47 |
-Current | 1277 (44.6%) | 900 (30.7%) | 6.67, 5.59–7.96 |
Diesel exhaust * | |||
-No | 2108 (73.7%) | 2289 (78.0%) | Ref |
-Yes | 753 (26.3%) | 647 (22.0%) | 1.15, 1.01–1.33 |
Crystalline silica * | |||
-No | 2694 (94.2%) | 2827 (96.3%) | Ref |
-Yes | 167 (5.84%) | 109 (3.71%) | 1.75, 1.33–2.31 |
Welding fumes * | |||
-No | 1783 (62.3%) | 2013 (68.6%) | Ref |
-Yes | 1078 (37.7%) | 923 (31.4%) | 1.18, 1.04–1.35 |
Education † | |||
-Low | 402 (14.1%) | 582 (19.9%) | Ref |
-Medium | 2026 (70.9%) | 2007 (68.5%) | 1.34, 1.15–1.56 |
-High | 427 (15.0%) | 341 (11.6%) | 1.74, 1.38–2.19 |
OR and 95% CI of Lung Cancer | ||||||||
---|---|---|---|---|---|---|---|---|
Diesel Exhaust | Crystalline Silica | Welding Fumes | Any | |||||
aOR (95% CI) | OR (95% CI) | aOR (95% CI) | OR (95% CI) | aOR (95% CI) | OR (95% CI) | aOR | OR | |
NDE | 1.26 (1.04–1.53) | 1.29 (1.11–1.51) | 1.27 (1.05–1.53) | 1.33 (1.14–1.54) | 1.26 (1.04–1.52) | 1.29 (1.10–1.50) | 1.42 (1.20–1.67) | 1.28 (1.10–1.49) |
NIE | 1.02 (0.98–1.06) | 1.04 (1.01–1.06) | 1.01 (1.00–1.02) | 1.01 (1.00–1.02) | 1.03 (0.97–1.09) | 1.04 (1.02–1.06) | 1.06 (1.00–1.12) | 1.04 (1.02–1.07) |
TE | 1.29 (1.06–1.56) | 1.34 (1.15–1.56) | 1.28 (1.06–1.55) | 1.34 (1.15–1.56) | 1.29 (1.06–1.57) | 1.34 (1.25–1.56) | 1.50 (1.26–1.78) | 1.34 (1.15–1.56) |
PM | 7.8% | 12.5% | 4.9% | 3.4% | 10.8% | 13.3% | 13.4% | 14.8% |
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Collatuzzo, G.; Teglia, F.; Boffetta, P. Role of Occupation in Shaping Cancer Disparities. Cancers 2022, 14, 4259. https://doi.org/10.3390/cancers14174259
Collatuzzo G, Teglia F, Boffetta P. Role of Occupation in Shaping Cancer Disparities. Cancers. 2022; 14(17):4259. https://doi.org/10.3390/cancers14174259
Chicago/Turabian StyleCollatuzzo, Giulia, Federica Teglia, and Paolo Boffetta. 2022. "Role of Occupation in Shaping Cancer Disparities" Cancers 14, no. 17: 4259. https://doi.org/10.3390/cancers14174259
APA StyleCollatuzzo, G., Teglia, F., & Boffetta, P. (2022). Role of Occupation in Shaping Cancer Disparities. Cancers, 14(17), 4259. https://doi.org/10.3390/cancers14174259