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Reducing Canadian Colorectal
Cancer Mortality Through Screening In 1998, following discussion with experts and stakeholders in Canada, Health Canada established a National Committee on Colorectal Cancer Screening comprised of members from provinces and key organizations from across the country. The Committee's mandate was to explore the scope and issues surrounding population-based colorectal cancer (CRC) screening, and to develop a set of final recommendations. During its 2 years, the Committee examined evidence from randomized controlled trials (RCTs) and statistical modeling. The Committee also reviewed recommendations/reports from other countries which had undertaken similar evaluations, and information from expert opinion. Throughout the process, the Committee members were encouraged to identify issues or gaps in data/knowledge for which they required more information to formulate the final set of recommendations. (A companion document, Technical Report for the National Committee on CRC Screening, presents the technical information that was considered over the 2 years). The National Committee came to a consensus and developed its recommendations for population-based CRC screening in Canada. Evidence, Information and Issues Considered for Recommendations Based on evidence from available randomized controlled trials1-4, the National Committee agreed that there was strong evidence to support that fecal occult blood screening could reduce CRC mortality by 15% to 33% in a targeted population of 50 to 74 year olds. Since an estimated 6,400 CRC deaths were expected to occur in Canada in 2001, and since the majority of these would be among Canadians aged 50 or older, the National Committee believed there could be a substantial potential for population benefit with CRC screening. However the National Committee also recognized that CRC screening carries some risks and opportunity costs. Among the various tests which have been used for screening, only the Fecal Occult Blood Test (FOBT), to date, has been shown to be effective and evaluated in randomized trials as the initial screening test. By itself, and used alone, it carries negligible risk; nonetheless, follow-up with colonoscopy (as has been the practice in most RCT's), presents low but measurable risks of serious complications. The issue of follow-up with another test is important because FOBTs are associated with false positive results.5 The Population Health Model (POHEM) developed by Statistics Canada estimated that 75 deaths and 611 perforations could result from diagnostic colonoscopy with a biennial screening program that starts in Canada in 2000 and ends in 2009. This is in contrast to an estimated reduction in CRC mortality of 16.7% (or 7,740 deaths) with biennial screening over the same 10 year period. At the individual level, the lifetime probability of death from CRC would fall from 0.29% to 0.19% for an individual who participates in all screening events, of a biennial program, from the age of 50 to 74; the lifetime risk of colonoscopy-induced death would be 0.005% for that same individual. Clearly, these estimates are difficult to verify/quantify at the population-level, as most studies reporting colonoscopy complications are carried out in patient groups that include symptomatic individuals. The risks among a healthy screening population are so low that they are difficult to estimate from the RCT's presented to date. Nevertheless, the National Committee concluded that while the benefits clearly outweigh the risks, any individual contemplating screening with the FOBT should be made aware of both the risks and benefits prior to the initial screen, and should give an informed consent to be screened. For a screening test to have a population-based impact, there must be adequate uptake (i.e. participation) in the target population. Thus, the National Committee evaluated the potential acceptability of the test and concluded that there was little or no information available on the likely participation rate that could be expected with a biennial screening program. In the RCTs to date1-4, adherence to the initial screening test (the FOBT) ranged from 53% to 67% in non-volunteer populations, with 38% to 46% of those invited completing all of the recommended screening and diagnostic tests. However, participation rates in RCTs, where the test efficacy is questionable by definition, may be different than when the test is proven to have a mortality benefit. Finally, the National Committee recognized that any recommendations about population-based CRC screening will have resource implications. Resources may differ among provinces so provincial strategies may need to take this into account. Prime resource impacts include the costs of the initial medical consultation prior to taking the FOBT, and the availability of resources for colonoscopy or other follow-up diagnostic tests, such as double contrast barium enema or flexible sigmoidscopy for some geographic areas. Based on participation and re-screen rates of 67% and 93% respectively among Canadians aged 50 to 74, the POHEM estimated the cost-effectiveness of a biennial FOBT screening program to be $11,907 per life year gained. The literature has reported that screening average risk individuals for CRC is as cost-effective as screening for other cancers.6 The cost per life year gained has been quoted at $20,000 (US), which falls well within the range of commonly accepted, cost-effective screening programs.7 The National Committee strongly urges the need for regular, periodic review of new technologies for CRC screening. Furthermore, the National Committee also stresses the importance of on-going research into CRC and evaluation of CRC prevention interventions. As a result of the aforementioned, the National Committee therefore recommends that:
These recommendations represent the consensus opinion of the group, with the exception of one participant. This participant did not feel that population-based screening should be promulgated if there was a possibility to do serious harm. The remainder of the participants acknowledged this risk, but felt that it was outweighed by the possibility of benefit. Consequently, the majority opinion was that this information should be provided to individuals for their own informed decision making. The recommendations represent the overall consensus of the individual Committee members, and not necessarily the endorsement by the respective organizations. (See Appendix A of the Technical Report for membership list.)
[Population-based Colorectal Cancer Screening]
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Last Updated: 2002-12-20 | ![]() |