Incidence trends in lung and bladder cancers in the Nordic Countries before and after the smoking epidemic
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
34074862
DOI
10.1097/cej.0000000000000694
PII: 00008469-202205000-00002
Knihovny.cz E-zdroje
- MeSH
- incidence MeSH
- kouření škodlivé účinky epidemiologie MeSH
- lidé MeSH
- nádory močového měchýře * epidemiologie etiologie MeSH
- plíce MeSH
- registrace MeSH
- věkové rozložení MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Dánsko epidemiologie MeSH
- Finsko epidemiologie MeSH
- Skandinávie a severské státy epidemiologie MeSH
- Švédsko epidemiologie MeSH
Cigarette smoking epidemic, which started before the World War II, completely changed the cancer landscape. Reliable incidence data spanning the stepwise spreading epidemic are rare, but the Nordic cancer registries are unique sources in being able to catch the pre-epidemic situation in the female population where smoking became more prevalent after the War. For Swedish men, smoking prevalence has decease early and cancer rates may herald postsmoking rates. We used data from the NORDCAN database, constructed by the cancer registries of Denmark, Finland, Norway and Sweden, for the analysis of incidence changes in lung and bladder cancers from year 1943 (Denmark), from 1953 (Finland and Norway) and from 1960 (Sweden) until year 2016. The analyses revealed four novel observation relevant to the smoking epidemic. (1) The incidence of lung cancer in Norwegian women in the 1950s, when the smoking prevalence was very low, was 1.8/100 000 (world standard rate), which is at the level of lowest global female rates known to-date; (2) the earliest lung-to-bladder incidence ratio among Norwegian women was 0.64, probably benchmarking the incidence rates prior to the smoking epidemic; (3) bladder cancer incidence for Finnish women diagnosed in the 1950s was 1.2/100 000 which is at the level of the lowest rates currently known and (4) Swedish men with the lowest smoking prevalence in Europe, showed an epochal crossing of lung and bladder cancer incidence rates before year 2015. The data suggest that the approaching of the incidence rates for lung and bladder cancer can be expected in the course of the abating smoking epidemic.
Biomedical Center Faculty of Medicine Charles University in Pilsen Pilsen Czech Republic
Cancer Gene Therapy Group Translational Immunology Research Program University of Helsinki
Comprehensive Cancer Center Helsinki University Hospital Helsinki Finland
Department of surgical and perioperative sciences Urology and andrology Umeå University Umeå Sweden
Department of Urology Helsinki University Hospital and University of Helsinki Helsinki Finland
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Pediatric Neurooncology German Cancer Research Center Heidelberg Germany
Zobrazit více v PubMed
Andersen ZJ, Jørgensen JT, Grøn R, Brauner EV, Lynge E (2017). Active smoking and risk of breast cancer in a Danish nurse cohort study. BMC Cancer. 17:556.
Andersson TM, Engholm G, Brink AL, Pukkala E, Stenbeck M, Tryggvadottir L, et al. (2018). Tackling the tobacco epidemic in the Nordic countries and lower cancer incidence by 1/5 in a 30-year period-the effect of envisaged scenarios changing smoking prevalence. Eur J Cancer. 103:288–298.
Brown KF, Rumgay H, Dunlop C, Ryan M, Quartly F, Cox A, et al. (2018). The fraction of cancer attributable to modifiable risk factors in England, Wales, Scotland, Northern Ireland, and the United Kingdom in 2015. Br J Cancer. 118:1130–1141.
Clemmensen KK, Lynge E, Clemmensen IH (2012). Nationwide tobacco surveys and sales data in Denmark from 1920 to 2010. Dan Med J. 59:A4448.
Collaborators, Global Burden of Disease Tobacco (2017). Smoking prevalence and attributable disease burden in 195 countries and territories, 1990-2015: a systematic analysis from the Global Burden of Disease Study 2015. Lancet. 389: 1885–1906.
Dobruch J, Daneshmand S, Fisch M, Lotan Y, Noon AP, Resnick MJ, et al. (2016). Gender and bladder cancer: a collaborative review of etiology, biology, and outcomes. Eur Urol. 69:300–310.
Engholm G, Ferlay J, Christensen N, Bray F, Gjerstorff ML, Klint A, et al. (2010). NORDCAN--a Nordic tool for cancer information, planning, quality control and research. Acta Oncol. 49:725–736.
Frank C, Fallah M, Ji J, Sundquist J, Hemminki K (2014). The population impact of familial cancer, a major cause of cancer. Int J Cancer. 134:1899–1906.
IARC (2004). Tobacco Smoke and Involuntary Smoking. Lyon: IARC.
IARC (2012). Personal Habits and Indoor Combustions . vol. 100E. Lyon: International Agency for Research on Cancer.
Islami F, Torre LA, Jemal A (2015). Global trends of lung cancer mortality and smoking prevalence. Transl Lung Cancer Res. 4:327–338.
Jäppinen P, Tola S (1986). Smoking among Finnish pulp and paper workers--evaluation of its confounding effect on lung cancer and coronary heart disease rates. Scand J Work Environ Health. 12:619–626.
Kraft P, Svendsen T, Hauknes A (1998). Intention to stop smoking among Norwegian smokers: the role of nicotine dependence, type of cigarettes, and age at onset of daily smoking. Addict Behav. 23:133–137.
Lee PN (2018). Tar level of cigarettes smoked and risk of smoking-related diseases. Inhal Toxicol. 30:5–18.
Lee PN, Thornton AJ, Hamling JS (2016). Epidemiological evidence on environmental tobacco smoke and cancers other than lung or breast. Regul Toxicol Pharmacol. 80:134–163.
Li Y, Tindle HA, Hendryx MS, Xun P, He K, Liang X, Luo J (2019). Smoking Cessation and the Risk of Bladder Cancer among Postmenopausal Women. Cancer Prev Res (Phila). 12:305–314.
Lipfert FW, Wyzga RE (2019). Longitudinal relationships between lung cancer mortality rates, smoking, and ambient air quality: a comprehensive review and analysis. Crit Rev Toxicol. 49:790–818.
Liu X, Hemminki K, Forsti A, Sundquist K, Sundquist J, Ji J (2015). Cancer risk in patients with type 2 diabetes mellitus and their relatives. Int J Cancer.
Lund I, Lund KE (2014). Lifetime smoking habits among Norwegian men and women born between 1890 and 1994: a cohort analysis using cross-sectional data. BMJ Open. 4:e005539.
Lund KE, Vedøy TF, Bauld L (2017). Do never smokers make up an increasing share of snus users as cigarette smoking declines? Changes in smoking status among male snus users in Norway 2003-15. Addiction. 112:340–348.
Malmstrom PU, Gardmark T, Sherif A, Strock V, Hosseini, Aliabad A, Jahnson S, et al. (2019). Incidence, survival and mortality trends of bladder cancer in Sweden 1997-2016. Scand J Urol. 53:193–199.
Marcos-Gragera R, Mallone S, Kiemeney LA, Vilardell L, Malats N, Allory Y, Sant M (2015). Urinary tract cancer survival in Europe 1999-2007: results of the population-based study EUROCARE-5. Eur J Cancer. 51:2217–2230.
Norberg M, Lundqvist G, Nilsson M, Gilljam H, Weinehall L (2011). Changing patterns of tobacco use in a middle-aged population: the role of snus, gender, age, and education. Glob Health Action. 4.
Osler M (1992). Smoking habits in Denmark from 1953 to 1991: a comparative analysis of results from three nationwide health surveys among adult Danes in 1953-1954, 1986-1987 and 1990-1991. Int J Epidemiol. 21:862–871.
Patja K, Hakala SM, Boström G, Nordgren P, Haglund M (2009). Trends of tobacco use in Sweden and Finland: do differences in tobacco policy relate to tobacco use? Scand J Public Health. 37:153–160.
Polednak AP (1994). Trends in cancer incidence in Connecticut, 1935-1991. Cancer. 74:2863–2872.
Proctor RN (2001). Tobacco and the global lung cancer epidemic. Nat Rev Cancer. 1:82–86.
Pukkala E, Engholm G, Hojsgaard Schmidt LK, Storm H, Khan S, Lambe M, et al. (2018). Nordic Cancer Registries - an overview of their procedures and data comparability. Acta Oncol. 57:440–455.
Roupret M, Babjuk M, Comperat E, Zigeuner R, Sylvester RJ, Burger M, et al. (2018). European association of urology guidelines on upper urinary tract urothelial carcinoma: 2017 update. Eur Urol. 73:111–122.
Shopland DR (1995). Tobacco use and its contribution to early cancer mortality with a special emphasis on cigarette smoking. Environ Health Perspect. 103 (Suppl 8):131–142.
Siegel R, Naishadham D, Jemal A (2012). Cancer statistics, 2012. CA Cancer J Clin. 62:10–29.
Tenkanen L, Hakulinen T, Hakama M, Saxén E (1985). Sauna, dust and migration as risk factors in lung cancer among smoking and non-smoking males in Finland. Int J Cancer. 35:637–642.
Tindle HA, Stevenson Duncan M, Greevy RA, Vasan RS, Kundu S, Massion PP, Freiberg MS (2018). Lifetime smoking history and risk of lung cancer: results from the Framingham Heart Study. J Natl Cancer Inst. 110:1201–1207.
Tolstrup JS, Pisinger VSC, Egan KK, Christensen AI (2018). Trends in smoking and smokeless tobacco use among Danish Adolescents, 1997-2014. Tob Prev Cessat. 4:10.
Welty CJ, Wright JL, Hotaling JM, Bhatti P, Porter MP, White E (2014). Persistence of urothelial carcinoma of the bladder risk among former smokers: results from a contemporary, prospective cohort study. Urol Oncol. 32:25.e21–25.e25.
Survival in Lung Cancer in the Nordic Countries Through A Half Century
Survival in gastric and esophageal cancers in the Nordic countries through a half century
Incidence and survival in laryngeal and lung cancers in Finland and Sweden through a half century
Incidence and survival in oral and pharyngeal cancers in Finland and Sweden through half century
Survival in bladder and upper urinary tract cancers in Finland and Sweden through 50 years