Cost comparison of predictive genetic testing versus conventional clinical screening for familial adenomatous polyposis. Issue 5 (1st May 1999)

• Record Type: Journal Article
• Authors: Bapat, B; Noorani, H; Cohen, Z; Berk, T; Mitri, A; Gallie, B; Pritzker, K; Gallinger, S; Detsky, A S
• Is Part Of: Gut. Volume 44:Issue 5(1999)
• Page Start: 698
• Page End: 703
• Publication Date: 1999-05-01
• Subjects: familial adenomatous polyposis -- adenomatous polyposis coli gene -- cost analysis -- genetic testing; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gut.44.5.698
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : BACKGROUND: Mutations of the APC gene cause familial adenomatous polyposis (FAP), a hereditary colorectal cancer predisposition syndrome. AIMS: To conduct a cost comparison analysis of predictive genetic testing versus conventional clinical screening for individuals at risk of inheriting FAP, using the perspective of a third party payer. METHODS: All direct health care costs for both screening strategies were measured according to time and motion, and the expected costs evaluated using a decision analysis model. RESULTS: The baseline analysis predicted that screening a prototype FAP family would cost $4975/£3109 by molecular testing and $8031/£5019 by clinical screening strategy, when family members were monitored with the same frequency of clinical surveillance (every two to three years). Sensitivity analyses revealed that the genetic testing approach is cost saving for key variables including the kindred size, the age of screening onset, and the cost of mutation identification in a proband. However, if the APC mutation carriers were monitored at an increased (annual) frequency, the cost of the genetic screening strategy increased to $7483/£4677 and was especially sensitive to variability in age of onset of screening, family size, and cost of genetic testing of at risk relatives. CONCLUSIONS: In FAP kindreds, a predictive genetic testing strategy costs less than conventional clinical screening, provided that the frequency of surveillance is identical using either strategy. An additional significant benefit is the elimination of unnecessary colonic examinations for those family members found to be non-carriers.