Skip to main content
Canadian Journal of Gastroenterology logoLink to Canadian Journal of Gastroenterology
editorial
. 2012 Jul;26(7):417–418. doi: 10.1155/2012/507989

Tackling colorectal cancer as a public health issue: What can the gastroenterologist do?

Catherine Dubé 1,
PMCID: PMC3395440  PMID: 22803014

Colorectal cancer (CRC) is an important public health issue. It is the second leading cause of cancer death among Canadians (9200 estimated deaths in 2012), the third most common cancer diagnosis overall (23,300 estimated new cases in 2012) and it will be responsible for 13.3% of all new cancer diagnoses in Canada this year (1). CRC lends itself particularly well to screening because it is a slowly progressive disease that is asymptomatic in its early stages, affecting a well-described target population and can be cured if treated early. Moreover, there is very good evidence supporting the effectiveness of screening for reducing CRC incidence as well as CRC-related mortality, yielding mortality reductions ranging between 12% and 43% depending on the screening modality and data analysis (2,3). Organized CRC screening is also cost effective (46). In fact, of all cancer screening interventions, CRC screening is recognized as one of the most effective. Yet, screening rates remain low in Canada. The 2008 Canadian Community Health Survey revealed that only 32% (range 16% to 46%) of Canadians 50 to 74 years of age reported having undergone either a fecal occult blood test in the past two years or a sigmoidoscopy/colonoscopy in the past five years for nonsymptomatic reasons (7).

In the current issue of the Canadian Journal of Gastroenterology, Wang et al (8) (pages 419–423) from Edmonton (Alberta) report on the CRC screening delay in average-risk individuals as well as those with a positive family history. Organized CRC screening has yet to be implemented in Alberta, such that CRC screening occurs in an opportunistic fashion (ie, either being initiated by patients or through recommendation from their treating physician[s]). There was a delay in the time to first screening of 14.4 years and 8.2 years in those with a significant family history of CRC and those at average risk, respectively. When questioned about the perceived risk of CRC, 56.2% and 42.7% of those with a family history and of those at average risk, respectively, rated their risk inappropriately, most of the time underestimating that risk. These findings are supported by a recent pan-Canadian survey of 4050 Canadians 45 to 74 years of age on their understanding and attitudes toward getting screened for CRC. In this survey, 92% of Canadians agreed that cancer screening was a medical test to detect cancer; however, 53% mistakenly believed that initial screening should happen only after symptoms are noticed (9).

Multiple barriers can limit population participation, one of which, as identified by Wang et al, is the lack of patient awareness of their personal risk for CRC and the lack of initiation of screening by family doctors. However, there is also the need to move from an opportunistic model of screening to that of established programs that can monitor the participation in the target population and develop interventions to increase that participation. Ultimately, it is the achievement of a high level of participation that will impact CRC incidence and mortality. As a reference, the European Guidelines for Quality Assurance in Colorectal Cancer Screening and Diagnosis (10) recommend to achieve a participation rate of at least 65% among the target population.

While public health and primary care should be devoting efforts toward increasing awareness of and participation in screening, gastroenterologists and endoscopists are faced with other issues such as maintaining the fine balance between timely access to care for patients with symptoms while ensuring that CRC screening can effectively take place. This becomes particularly challenging when gastroenterologists recommend that screening of the average-risk population be performed using colonoscopy because limitations in infrastructure and manpower make this approach to CRC screening practically incompatible with the goal of reaching participation rates of at least 65%. Up until recently, this dilemma was a significant cause of limited access to screening: primary care physicians and gastroenterologists alike have little confidence in the traditional guaiac-based fecal occult blood test, leading to a preference for screening colonoscopy. However, with the availability of the more sensitive fecal immunochemical test (FIT), this tension between screening and acute care can hopefully be resolved because FIT represents a reasonable alternative to colonoscopy for screening of the average-risk population (4,5,1113). Depending on the cut-off for FIT positivity and the number of samples taken, the number needed to colonoscope to diagnose a CRC from a population of FIT-positive individuals varies between 9.8 and 18.5 (11,14). This is in contrast to the number needed to colonoscope from a population of average-risk individuals, which ranges between 191 and 240 (11, personal communication: A Rostom, Forzani & MacPhail Colon Cancer Screening Centre, Department of Gastroenterology, University of Calgary, Calgary, Alberta). This not only frees endoscopy space, but also reduces the exposure of the screened population to the risks of complications from colonoscopy.

Gastroenterologists and endoscopists at large need to approach CRC as a public health problem, sharing the ultimate goal to reduce CRC-related morbidity and mortality in the population through CRC screening. In this optic, they should support and recommend the screening modality that optimizes the balance between access (to optimize population participation) and ability to detect CRC. Freeing endoscopy space by restricting screening-related colonoscopies to individuals with abnormal FIT results, higher-risk individuals, and to those requiring adenoma and/or CRC surveillance, will significantly reduce the tension created by the competing demands between acute care and screening. Once access to colonoscopy can be assured, is it then possible for public health initiatives to successfully promote and facilitate CRC screening to formally institute organized screening without fear of creating backlogs for acute care gastroenterology. This, in turn, will finally enable us to effectively participate in reducing the burden of CRC in the population.

REFERENCES

  • 1.Canadian Cancer Society’s Steering Committee on Cancer Statistics . Canadian Cancer Statistics 2012. Toronto: Canadian Cancer Society; 2012. [Google Scholar]
  • 2.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;103:1541–9. doi: 10.1111/j.1572-0241.2008.01875.x. [DOI] [PubMed] [Google Scholar]
  • 3.Atkin WS, Edwards R, Kralj-Hans I, et al. Once-only flexible sigmoidoscopy screening in prevention of colorectal cancer: A multicentre randomized controlled trial. Lancet. 2010;375:1624–33. doi: 10.1016/S0140-6736(10)60551-X. [DOI] [PubMed] [Google Scholar]
  • 4.Zauber AG, Lansdorp-Vogelaar I, Knudsen AB, Wilschut J, Van BM, Kuntz KM. Evaluating test strategies for colorectal cancer screening: A decision analysis for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;149:659–69. doi: 10.7326/0003-4819-149-9-200811040-00244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Heitman SJ, Hilsden RJ, Au F, Dowden S, Manns BJ. Colorectal cancer screening for average-risk North Americans: An economic evaluation. PLoS Med. 2010;7:e1000370. doi: 10.1371/journal.pmed.1000370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Sharp L, Tilson L, Whyte S, et al. Cost-effectiveness of population-based screening for colorectal cancer: A comparison of guaiac-based faecal occult blood testing, faecal immunochemical testing and flexible sigmoidoscopy. Br J Cancer. 2012;106:805–16. doi: 10.1038/bjc.2011.580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Canadian Community Health Survey . Ottawa: Statistics Canada; 2008. [Google Scholar]
  • 8.Wang H, Gies N, Wong C, Sadowski D, Moysey B, Fedorak R. Patients undergoing colorectal cancer screening underestimate their cancer risk and delay presentation for screening. Can J Gastroenterol. 2012;26:419–23. doi: 10.1155/2012/937184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Canadian Partnership Against Cancer, Canadians’ Awareness and Attitudes towards Colorectal Cancer Screening. Jan, 2012.
  • 10.European Commission . European guidelines for quality assurance in colorectal cancer screening and diagnosis, – 1st edn. In: Segnan N, Patnick J, von Karsa L, editors. Luxembourg: Publications Office of the European Union; 2012. [DOI] [PubMed] [Google Scholar]
  • 11.Quintero E, Castells A, Bujanda L, Cubiella J, et al. Colonoscopy versus fecal immunochemical testing in colorectal-cancer screening. N Engl J Med. 2012;366:697–706. doi: 10.1056/NEJMoa1108895. [DOI] [PubMed] [Google Scholar]
  • 12.van Rossum LG, van Rijn AF, Laheij RJ, et al. Random comparison of guaiac and immunochemical fecal occult blood tests for colorectal cancer in a screening population. Gastroenterology. 2008;135:82–90. doi: 10.1053/j.gastro.2008.03.040. [DOI] [PubMed] [Google Scholar]
  • 13.Hol L, van Leerdam ME, Van BM, et al. Screening for colorectal cancer: Randomised trial comparing guaiac-based and immunochemical faecal occult blood testing and flexible sigmoidoscopy. Gut. 2010;59:62–8. doi: 10.1136/gut.2009.177089. [DOI] [PubMed] [Google Scholar]
  • 14.van Roon AHC, Wilschut JA, Hol L, et al. Diagnostic yield improves with collection of 2 samples in fecal immunochemical test screening without affecting attendance. Clin Gastroenterol Hepatol. 2011;9:333–9. doi: 10.1016/j.cgh.2010.12.012. [DOI] [PubMed] [Google Scholar]

Articles from Canadian Journal of Gastroenterology are provided here courtesy of Wiley

RESOURCES