No retraction, correction or concern found when last checked on Oct 19, 2026.
The colorectal cancer epidemic: challenges and opportunities for primary, secondary and tertiary prevention
Hermann Brenner, Chen Chen
British Journal of Cancer · 2018 · Review
Abstract
Colorectal cancer (CRC) is both one of the most common and one of the most preventable cancers globally, with powerful but strongly missed potential for primary, secondary and tertiary prevention. CRC incidence has traditionally been the highest in affluent Western countries, but it is now increasing rapidly with economic development in many other parts of the world. CRC shares several main risk factors, such as smoking, excessive alcohol consumption, physical inactivity and being overweight, with other common diseases; therefore, primary prevention efforts to reduce these risk factors are expected to have multiple beneficial effects that extend beyond CRC prevention, and should have high public health impact. A sizeable reduction in the incidence and mortality of CRC can also be achieved by offering effective screening tests, such as faecal immunochemical tests, flexible sigmoidoscopy and colonoscopy, in organised screening programmes which have been implemented in an increasing number of countries. Countries with early and high uptake rates of effective screening have exhibited major declines in CRC incidence and mortality, in contrast to most other countries. Finally, increasing evidence shows that the prognosis and quality of life of CRC patients can be substantially improved by tertiary prevention measures, such as the administration of low-dose aspirin and the promotion of physical activity.
References 103
- 1.
Ferlay J, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int. J. Cancer. 2015;136:E359-386.
Not in our library10.1002/ijc.29210
- 2.
Babaei M, et al. Minimally invasive colorectal cancer surgery in Europe: implementation and outcomes. Med. (Baltim.). 2016;95:e3812.
Not in our library10.1097/md.0000000000003812
- 3.
Brenner H, Kloor M, Pox CP. Colorectal cancer. Lancet. 2014;383:1490-1502.
Not in our library10.1016/s0140-6736(13)61649-9
- 4.
Babaei M, et al. Neoadjuvant therapy in rectal cancer patients with clinical Stage II to III across European countries: variations and outcomes. Clin. Colorectal Cancer. 2018;17:e129-e142.
Not in our library10.1016/j.clcc.2017.09.002
- 5.
Babaei M, et al. Administration of adjuvant chemotherapy for stage II-III colon cancer patients: an European population-based study. Int. J. Cancer. 2018;142:1480-1489.
Not in our library10.1002/ijc.31168
- 6.
Jemal, A. et al. Annual report to the nation on the status of cancer, 1975–2014, featuring survival. J. Natl. Cancer Inst. 109 (2017).
Not in our library10.1093/jnci/djx030
- 7.
Holleczek B, et al. On-going improvement and persistent differences in the survival for patients with colon and rectum cancer across Europe 1999–2007—Results from the EUROCARE-5 study. Eur. J. Cancer. 2015;51:2158-2168.
Not in our library10.1016/j.ejca.2015.07.024
- 8.
Siegel RL, et al. Colorectal cancer statistics, 2017. CA Cancer J. Clin. 2017;67:177-193.
Not in our library10.3322/caac.21395
- 9.
Arnold M, et al. Global patterns and trends in colorectal cancer incidence and mortality. Gut. 2017;66:683-691.
Not in our library10.1136/gutjnl-2015-310912
- 10.
Brenner H, Schrotz-King P, Holleczek B, Katalinic A, Hoffmeister M. Declining bowel cancer incidence and mortality in Germany: an analysis of time trends in the first ten years after the introduction of screening colonoscopy. Dtsch. Ärzteblatt Int. 2016;113:101-106.
Not in our library10.3238/arztebl.2016.0101
- 11.
Chen C, Lacke E, Stock C, Hoffmeister M, Brenner H. Colonoscopy and sigmoidoscopy use among older adults in different countries: a systematic review. Prev. Med. 2017;103:33-42.
Not in our library10.1016/j.ypmed.2017.07.021
- 12.
Siegel, R. L. et al. Colorectal cancer incidence patterns in the United States, 1974–2013. J. Natl. Cancer Inst. 109 (2017).
Not in our library10.1093/jnci/djw322
- 13.
Botteri E, et al. Smoking and colorectal cancer: a meta-analysis. JAMA. 2008;300:2765-2778.
Not in our library10.1001/jama.2008.839
- 14.
Bagnardi V, et al. Alcohol consumption and site-specific cancer risk: a comprehensive dose-response meta-analysis. Br. J. Cancer. 2015;112:580-593.
Not in our library10.1038/bjc.2014.579
- 15.
Freisling H, et al. Comparison of general obesity and measures of body fat distribution in older adults in relation to cancer risk: meta-analysis of individual participant data of seven prospective cohorts in Europe. Br. J. Cancer. 2017;116:1486-1497.
Not in our library10.1038/bjc.2017.106
- 16.
Vieira AR, et al. Foods and beverages and colorectal cancer risk: a systematic review and meta-analysis of cohort studies, an update of the evidence of the WCRF-AICR continuous update project. Ann. Oncol. 2017;28:1788-1802.
Not in our library10.1093/annonc/mdx171
- 17.
Boyle T, Keegel T, Bull F, Heyworth J, Fritschi L. Physical activity and risks of proximal and distal colon cancers: a systematic review and meta-analysis. J. Natl. Cancer Inst. 2012;104:1548-1561.
Not in our library10.1093/jnci/djs354
- 18.
Algra AM, Rothwell PM. Effects of regular aspirin on long-term cancer incidence and metastasis: a systematic comparison of evidence from observational studies versus randomised trials. Lancet Oncol. 2012;13:518-527.
Not in our library10.1016/s1470-2045(12)70112-2
- 19.
Cao Y, et al. Population-wide impact of long-term use of aspirin and the risk for cancer. JAMA Oncol. 2016;2:762-769.
Not in our library10.1001/jamaoncol.2015.6396
- 20.
Green J, et al. Menopausal hormone therapy and risk of gastrointestinal cancer: nested case-control study within a prospective cohort, and meta-analysis. Int. J. Cancer. 2012;130:2387-2396.
Not in our library10.1002/ijc.26236
- 21.
http://www.tobaccoatlas.org/topic/cigarette-use-globally/ Accessed 3 Jan 2018.
Not in our library
- 22.
- 23.
Young JP, et al. Rising incidence of early-onset colorectal cancer in Australia over two decades: report and review. J. Gastroenterol. Hepatol. 2015;30:6-13.
Not in our library10.1111/jgh.12792
- 24.
Hidayat K, Yang CM, Shi BM. Body fatness at an early age and risk of colorectal cancer. Int. J. Cancer. 2018;142:729-740.
Not in our library10.1002/ijc.31100
- 25.
Ogino S, Chan AT, Fuchs CS, Giovannucci E. Molecular pathological epidemiology of colorectal neoplasia: an emerging transdisciplinary and interdisciplinary field. Gut. 2011;60:397-411.
Not in our library10.1136/gut.2010.217182
- 26.
Hughes LAE, Simons CCJM, van den Brandt PA, van Engeland M, Weijenberg MP. Lifestyle, diet, and colorectal cancer risk according to (Epi)genetic instability: current evidence and future directions of molecular pathological epidemiology. Curr. Colorectal Cancer Rep. 2017;13:455-469.
Not in our library10.1007/s11888-017-0395-0
- 27.
Rescigno, T., Micolucci, L., Tecce, M. F., Capasso, A. Bioactive nutrients and nutrigenomics in age-related diseases. Molecules22, pii: E105 (2017).
Not in our library10.3390/molecules22010105
- 28.
Slattery ML, et al. Infrequently expressed miRNAs in colorectal cancer tissue and tumor molecular phenotype. Mod. Pathol. 2017;30:1152-1169.
Not in our library10.1038/modpathol.2017.38
- 29.
Ogino S, et al. Integrative analysis of exogenous, endogenous, tumour and immune factors for precision medicine. Gut. 2018;67:1168-1180.
Not in our library10.1136/gutjnl-2017-315537
- 30.
Carr PR, et al. Lifestyle factors and risk of sporadic colorectal cancer by microsatellite instability status: a systematic review and meta-analyses. Ann. Oncol. 2018;29:825-834.
Not in our library10.1093/annonc/mdy059
- 31.
Oosterhoff M, Joore M, Ferreira I. The effects of school-based lifestyle interventions on body mass index and blood pressure: a multivariate multilevel meta-analysis of randomized controlled trials. Obes. Rev. 2016;17:1131-1153.
Not in our library10.1111/obr.12446
- 32.
Bibbins-Domingo K. Aspirin use for the primary prevention of cardiovascular disease and colorectal cancer: U.S. preventive services task force recommendation statement. Ann. Intern. Med. 2016;164:836-845.
Not in our library10.7326/m16-0577
- 33.
Singh Ranger G. The role of aspirin in colorectal cancer chemoprevention. Crit. Rev. Oncol. Hematol. 2016;104:87-90.
Not in our library10.1016/j.critrevonc.2016.05.011
- 34.
Marjoribanks J, Farquhar C, Roberts H, Lethaby A, Lee J. Long-term hormone therapy for perimenopausal and postmenopausal women. Cochrane Database Syst. Rev. 2017;1:Cd004143.
Not in our library10.1002/14651858.cd004143.pub5
- 35.
Gartlehner G, et al. Hormone therapy for the primary prevention of chronic conditions in postmenopausal women: evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2017;318:2234-2249.
Not in our library10.1001/jama.2017.16952
- 36.
Brenner H, Altenhofen L, Stock C, Hoffmeister M. Natural history of colorectal adenomas: birth cohort analysis among 3.6 million participants of screening colonoscopy. Cancer Epidemiol. Biomark. Prev. 2013;22:1043-1051.
Not in our library10.1158/1055-9965.epi-13-0162
- 37.
Hewitson P, Glasziou P, Watson E, Towler B, Irwig L. Cochrane systematic review of colorectal cancer screening using the fecal occult blood test (hemoccult): an update. Am. J. Gastroenterol. 2008;103:1541-1549.
Not in our library10.1111/j.1572-0241.2008.01875.x
- 38.
Scholefield JH, Moss SM, Mangham CM, Whynes DK, Hardcastle JD. Nottingham trial of faecal occult blood testing for colorectal cancer: a 20-year follow-up. Gut. 2012;61:1036-1040.
Not in our library10.1136/gutjnl-2011-300774
- 39.
Shaukat A, et al. Long-term mortality after screening for colorectal cancer. N. Engl. J. Med. 2013;369:1106-1114.
Not in our library10.1056/nejmoa1300720
- 40.
Hol L, et al. Screening for colorectal cancer: randomised trial comparing guaiac-based and immunochemical faecal occult blood testing and flexible sigmoidoscopy. Gut. 2010;59:62-68.
Not in our library10.1136/gut.2009.177089
- 41.
Brenner H, Tao S. Superior diagnostic performance of faecal immunochemical tests for haemoglobin in a head-to-head comparison with guaiac based faecal occult blood test among 2235 participants of screening colonoscopy. Eur. J. Cancer. 2013;49:3049-3054.
Not in our library10.1016/j.ejca.2013.04.023
- 42.
Robertson DJ, et al. Recommendations on fecal immunochemical testing to screen for colorectal neoplasia: a consensus statement by the US Multi-Society Task Force on colorectal cancer. Am. J. Gastroenterol. 2017;112:37-53.
Not in our library10.1038/ajg.2016.492
- 43.
Gies Anton, Bhardwaj Megha, Stock Christian, Schrotz-King Petra, Brenner Hermann. Quantitative fecal immunochemical tests for colorectal cancer screening. International Journal of Cancer. 2018;143(2):234-244.
Not in our library10.1002/ijc.31233
- 44.
Rex DK, et al. Colorectal cancer screening: recommendations for physicians and patients from the U.S. Multi-Society Task Force on colorectal cancer. Gastroenterology. 2017;153:307-323.
Not in our library10.1053/j.gastro.2017.05.013
- 45.
Schreuders EH, et al. Colorectal cancer screening: a global overview of existing programmes. Gut. 2015;64:1637-1649.
Not in our library10.1136/gutjnl-2014-309086
- 46.
van der Vlugt M, et al. Adherence to colorectal cancer screening: four rounds of faecal immunochemical test-based screening. Br. J. Cancer. 2017;116:44-49.
Not in our library10.1038/bjc.2016.399
- 47.
Imperiale TF, et al. Multitarget stool DNA testing for colorectal-cancer screening. N. Engl. J. Med. 2014;370:1287-1297.
Not in our library10.1056/nejmoa1311194
- 48.
Brenner H, Werner S, Chen H. Multitarget stool DNA testing for colorectal-cancer screening. N. Engl. J. Med. 2014;371:184-185.
Not in our library10.1056/nejmc1405215
- 49.
Brenner H, Chen H. Fecal occult blood versus DNA testing: indirect comparison in a colorectal cancer screening population. Clin. Epidemiol. 2017;9:377-384.
Not in our library10.2147/clep.s136565
- 50.
Lin JS, et al. Screening for colorectal cancer: updated evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2016;315:2576-2594.
Not in our library10.1001/jama.2016.3332
- 51.
- 52.
Segnan N, et al. Once-only sigmoidoscopy in colorectal cancer screening: follow-up findings of the Italian Randomized Controlled Trial—SCORE. J. Natl. Cancer Inst. 2011;103:1310-1322.
Not in our library10.1093/jnci/djr284
- 53.
Holme O, et al. Effect of flexible sigmoidoscopy screening on colorectal cancer incidence and mortality: a randomized clinical trial. JAMA. 2014;312:606-615.
Not in our library10.1001/jama.2014.8266
- 54.
Schoen RE, et al. Colorectal-cancer incidence and mortality with screening flexible sigmoidoscopy. N. Engl. J. Med. 2012;366:2345-2357.
Not in our library10.1056/nejmoa1114635
- 55.
Brenner H, Stock C, Hoffmeister M. Effect of screening sigmoidoscopy and screening colonoscopy on colorectal cancer incidence and mortality: systematic review and meta-analysis of randomised controlled trials and observational studies. BMJ. 2014;348:g2467.
Not in our library10.1136/bmj.g2467
- 56.
Kaminski MF, et al. The NordICC Study: rationale and design of a randomized trial on colonoscopy screening for colorectal cancer. Endoscopy. 2012;44:695-702.
Not in our library10.1055/s-0032-1306895
- 57.
Doubeni CA, et al. Effectiveness of screening colonoscopy in reducing the risk of death from right and left colon cancer: a large community-based study. Gut. 2018;67:291-298.
Not in our library10.1136/gutjnl-2016-312712
- 58.
Brenner H, Stock C, Hoffmeister M. In the era of widespread endoscopy use, randomized trials may strongly underestimate the effects of colorectal cancer screening. J. Clin. Epidemiol. 2013;66:1144-1150.
Not in our library10.1016/j.jclinepi.2013.05.008
- 59.
Chen C, Stock C, Hoffmeister M, Brenner H. Public health impact of colonoscopy use on colorectal cancer mortality in Germany and the United States. Gastrointest. Endosc. 2018;87:213-221.e212.
Not in our library10.1016/j.gie.2017.04.005
- 60.
Wolf AMD, et al. Colorectal cancer screening for average-risk adults: 2018 guideline update from the American Cancer Society. CA Cancer J. Clin. 2018;68:250-281.
Not in our library10.3322/caac.21457
- 61.
Frampton MJ, et al. Implications of polygenic risk for personalised colorectal cancer screening. Ann. Oncol. 2016;27:429-434.
Not in our library10.1093/annonc/mdv540
- 62.
Weigl K, et al. Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score. Clin. Epidemiol. 2018;10:143-152.
Not in our library10.2147/clep.s145636
- 63.
Jeon J, et al. Determining risk of colorectal cancer and starting age of screening based on lifestyle, environmental, and genetic factors. Gastroenterology. 2018;154:2152-2164.e19.
Not in our library10.1053/j.gastro.2018.02.021
- 64.
Weigl K, et al. Genetic risk score is associated with prevalence of advanced neoplasms in a colorectal cancer screening population. Gastroenterology. 2018;155:88-98.e10.
Not in our library10.1053/j.gastro.2018.03.030
- 65.
Lansdorp-Vogelaar I, Knudsen AB, Brenner H. Cost-effectiveness of colorectal cancer screening. Epidemiol. Rev. 2011;33:88-100.
Not in our library10.1093/epirev/mxr004
- 66.
van Hees F, et al. The value of models in informing resource allocation in colorectal cancer screening: the case of The Netherlands. Gut. 2015;64:1985-1997.
Not in our library10.1136/gutjnl-2015-309316
- 67.
Brenner H, Altenhofen L, Stock C, Hoffmeister M. Prevention, early detection, and overdiagnosis of colorectal cancer within 10 years of screening colonoscopy in Germany. Clin. Gastroenterol. Hepatol. 2015;13:717-723.
Not in our library10.1016/j.cgh.2014.08.036
- 68.
Knudsen AB, et al. Estimation of benefits, burden, and harms of colorectal cancer screening strategies: modeling study for the US Preventive Services Task Force. JAMA. 2016;315:2595-2609.
Not in our library10.1001/jama.2016.6828
- 69.
Lew JB, et al. Long-term evaluation of benefits, harms, and cost-effectiveness of the National Bowel Cancer Screening Program in Australia: a modelling study. Lancet Public Health. 2017;2:e331-e340.
Not in our library10.1016/s2468-2667(17)30105-6
- 70.
Walter V, Jansen L, Hoffmeister M, Brenner H. Smoking and survival of colorectal cancer patients: systematic review and meta-analysis. Ann. Oncol. 2014;25:1517-1525.
Not in our library10.1093/annonc/mdu040
- 71.
Walter V, et al. Smoking and survival of colorectal cancer patients: population-based study from Germany. Int. J. Cancer. 2015;137:1433-1445.
Not in our library10.1002/ijc.29511
- 72.
Ordonez-Mena JM, et al. Impact of prediagnostic smoking and smoking cessation on colorectal cancer prognosis: a meta-analysis of individual patient data from cohorts within the CHANCES consortium. Ann. Oncol. 2018;29:472-483.
Not in our library10.1093/annonc/mdx761
- 73.
Walter V, et al. Alcohol consumption and survival of colorectal cancer patients: a population-based study from Germany. Am. J. Clin. Nutr. 2016;103:1497-1506.
Not in our library10.3945/ajcn.115.127092
- 74.
Sharma A, et al. Tobacco smoking and postoperative outcomes after colorectal surgery. Ann. Surg. 2013;258:296-300.
Not in our library10.1097/sla.0b013e3182708cc5
- 75.
Dinicola S, et al. Nicotine increases survival in human colon cancer cells treated with chemotherapeutic drugs. Toxicol. Vitr. 2013;27:2256-2263.
Not in our library10.1016/j.tiv.2013.09.020
- 76.
Warren GW, et al. Nicotinic modulation of therapeutic response in vitro and in vivo. Int. J. Cancer. 2012;131:2519-2527.
Not in our library10.1002/ijc.27556
- 77.
Vincenzi B, et al. Cigarettes smoking habit may reduce benefit from cetuximab-based treatment in advanced colorectal cancer patients. Expert. Opin. Biol. Ther. 2009;9:945-949.
Not in our library10.1517/14712590903081694
- 78.
Cucina A, et al. Nicotine stimulates proliferation and inhibits apoptosis in colon cancer cell lines through activation of survival pathways. J. Surg. Res. 2012;178:233-241.
Not in our library10.1016/j.jss.2011.12.029
- 79.
Wei PL, et al. Nicotine enhances colon cancer cell migration by induction of fibronectin. Ann. Surg. Oncol. 2011;18:1782-1790.
Not in our library10.1245/s10434-010-1504-3
- 80.
Van Blarigan EL, Meyerhardt JA. Role of physical activity and diet after colorectal cancer diagnosis. J. Clin. Oncol. 2015;33:1825-1834.
Not in our library10.1200/jco.2014.59.7799
- 81.
Otto SJ, et al. Association of change in physical activity and body weight with quality of life and mortality in colorectal cancer: a systematic review and meta-analysis. Support. Care Cancer. 2015;23:1237-1250.
Not in our library10.1007/s00520-014-2480-0
- 82.
Walter V, et al. Physical activity and survival of colorectal cancer patients: Population-based study from Germany. Int. J. Cancer. 2017;140:1985-1997.
Not in our library10.1002/ijc.30619
- 83.
Friedenreich CM, Shaw E, Neilson HK, Brenner DR. Epidemiology and biology of physical activity and cancer recurrence. J. Mol. Med. 2017;95:1029-1041.
Not in our library10.1007/s00109-017-1558-9
- 84.
Lee J, Meyerhardt JA, Giovannucci E, Jeon JY. Association between body mass index and prognosis of colorectal cancer: a meta-analysis of prospective cohort studies. PLoS One. 2015;10:e0120706.
Not in our library10.1371/journal.pone.0120706
- 85.
Walter V, et al. Prognostic relevance of prediagnostic weight loss and overweight at diagnosis in patients with colorectal cancer. Am. J. Clin. Nutr. 2016;104:1110-1120.
Not in our library10.3945/ajcn.116.136531
- 86.
Carr PR, et al. Associations of red and processed meat with survival after colorectal cancer and differences according to timing of dietary assessment. Am. J. Clin. Nutr. 2016;103:192-200.
Not in our library10.3945/ajcn.115.121145
- 87.
van Zutphen M, Kampman E, Giovannucci EL, van Duijnhoven FJB. Lifestyle after colorectal cancer diagnosis in relation to survival and recurrence: a review of the literature. Curr. Colorectal Cancer Rep. 2017;13:370-401.
Not in our library10.1007/s11888-017-0386-1
- 88.
Van Blarigan EL, et al. Association of survival with adherence to the American Cancer Society Nutrition and Physical Activity Guidelines for Cancer Survivors after colon cancer diagnosis: the CALGB 89803/Alliance trial. JAMA Oncol. 2018;4:783-790.
Not in our library10.1001/jamaoncol.2018.0126
- 89.
Li P, et al. Aspirin use after diagnosis but not prediagnosis improves established colorectal cancer survival: a meta-analysis. Gut. 2015;64:1419-1425.
Not in our library10.1136/gutjnl-2014-308260
- 90.
Sostres C, Gargallo CJ, Lanas A. Aspirin, cyclooxygenase inhibition and colorectal cancer. World J. Gastrointest. Pharmacol. Ther. 2014;5:40-49.
Not in our library10.4292/wjgpt.v5.i1.40
- 91.
Frouws MA, et al. The mortality reducing effect of aspirin in colorectal cancer patients: Interpreting the evidence. Cancer Treat. Rev. 2017;55:120-127.
Not in our library10.1016/j.ctrv.2016.12.008
- 92.
- 93.
Weberpals J, Jansen L, Carr PR, Hoffmeister M, Brenner H. Beta blockers and cancer prognosis—The role of immortal time bias: a systematic review and meta-analysis. Cancer Treat. Rev. 2016;47:1-11.
Not in our library10.1016/j.ctrv.2016.04.004
- 94.
Garland CF, Gorham ED. Dose-response of serum 25-hydroxyvitamin D in association with risk of colorectal cancer: a meta-analysis. J. Steroid Biochem. Mol. Biol. 2017;168:1-8.
Not in our library10.1016/j.jsbmb.2016.12.003
- 95.
Zgaga L, et al. Plasma vitamin D concentration influences survival outcome after a diagnosis of colorectal cancer. J. Clin. Oncol. 2014;32:2430-2439.
Not in our library10.1200/jco.2013.54.5947
- 96.
Maalmi H, et al. Relationship of very low serum 25-hydroxyvitamin D3 levels with long-term survival in a large cohort of colorectal cancer patients from Germany. Eur. J. Epidemiol. 2017;32:961-971.
Not in our library10.1007/s10654-017-0298-z
- 97.
Ng K, et al. SUNSHINE: Randomized double-blind phase II trial of vitamin D supplementation in patients with previously untreated metastatic colorectal cancer. J. Clin. Oncol. 2017;35(15_suppl):3506.
Not in our library10.1200/jco.2017.35.15_suppl.3506
- 98.
Brenner H, Jansen L, Saum KU, Holleczek B, Schöttker B. Vitamin D supplementation trials aimed at reducing mortality have much higher power when focusing on people with low serum 25-hydroxyvitamin D concentrations. J. Nutr. 2017;147:1325-1333.
Not in our library10.3945/jn.117.250191
- 99.
World Cancer Research Fund, American Institute for Cancer Research. Continuous Update Project analysing research on cancer prevention and survival. Diet, nutrition, physical activity and colorectal cancer 2017. https://www.wcrf.org/sites/default/files/Colorectal-Cancer-2017-Report.pdf. Accessed 16 Mar 2018.
Not in our library
- 100.
The German Centre for Cancer Registry Data (ZfKD). https://www.krebsdaten.de/Krebs/EN/Database/databasequery_step1_node.html. Accessed 3 Feb 2018.
Not in our library
- 101.
U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2014 Incidence and Mortality Web-based Report. Atlanta: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute; 2017. https://nccd.cdc.gov/uscs/. Accessed 3 Feb 2018.
Not in our library
- 102.
The Netherlands Comprehensive Cancer Organisation (IKNL). The Netherlands Cancer Registry. https://www.cijfersoverkanker.nl/home-36.html. Accessed 3 Feb 2018.
Not in our library
- 103.
Office for National Statistics (ONS). Cancer Registration Statistics, England. https://www.ons.gov.uk/peoplepopulationandcommunity/healthandsocialcare/conditionsanddiseases/datasets/cancerregistrationstatisticscancerregistrationstatisticsengland. Accessed 3 Feb 2018.
Not in our library
Cited by papers we hold 1
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.