The use and interpretation of commercial APC gene testing for familial adenomatous polyposis.

BACKGROUND The use of commercially available tests for genes linked to familial cancer has aroused concern about the impact of these tests on patients. Familial adenomatous polyposis is an autosomal dominant disease caused by a germ-line mutation of the adenomatous polyposis coli (APC) gene that causes colorectal cancer if prophylactic colectomy is not performed. We evaluated the clinical use of commercial APC gene testing. METHODS We assessed indications for APC gene testing, whether informed consent was obtained and genetic counseling was offered before testing, and the interpretation of the results through telephone interviews with physicians and genetic counselors in a nationwide sample of 177 patients from 125 families who underwent testing during 1995. RESULTS Of the 177 patients tested, 83.0 percent had clinical features of familial adenomatous polyposis or were at risk for the disease-both valid indications for being tested. The appropriate strategy for presymptomatic testing was used in 79.4 percent (50 of 63 patients). Only 18.6 percent (33 of 177) received genetic counseling before the test, and only 16.9 percent (28 of 166) provided written informed consent. In 31.6 percent of the cases the physicians misinterpreted the test results. Among the patients with unconventional indications for testing, the rate of positive results was only 2.3 percent (1 of 44). CONCLUSIONS Patients who underwent genetic tests for familial adenomatous polyposis often received inadequate counseling and would have been given incorrectly interpreted results. Physicians should be prepared to offer genetic counseling if they order genetic tests.

[1]  K. Kahn,et al.  The use and misuse of upper gastrointestinal endoscopy. , 1988, Annals of internal medicine.

[2]  T. Smyrk,et al.  Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus. , 1992, American journal of human genetics.

[3]  L. Goldman,et al.  Ordering Patterns and Clinical Impact of Cardiovascular Nuclear Medicine Procedures , 1980, Circulation.

[4]  L. Goldman,et al.  Clinical utility and management impact of M-mode echocardiography. , 1983, The American journal of medicine.

[5]  G. Petersen,et al.  Genetic testing and counseling in familial adenomatous polyposis. , 1996, Oncology.

[6]  G. Guyatt,et al.  The contribution of a non-invasive test to clinical care. The impact of echocardiography on diagnosis, management and patient anxiety. , 1988, Journal of clinical epidemiology.

[7]  J. McPherson,et al.  Identification of deletion mutations and three new genes at the familial polyposis locus , 1991, Cell.

[8]  R. Lewontin,et al.  Pitfalls of genetic testing. , 1996, The New England journal of medicine.

[9]  H. Bussey,et al.  Familial polyposis coli. , 1975, Pathology annual.

[10]  M. Brown,et al.  The use of gene tests to detect hereditary predisposition to cancer: economic considerations. , 1995, Journal of the National Cancer Institute.

[11]  S. Bülow,et al.  Familial polyposis coli. , 1987, Seminars in surgical oncology.

[12]  Margaret Robertson,et al.  Identification and characterization of the familial adenomatous polyposis coli gene , 1991, Cell.

[13]  K. Kinzler,et al.  Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. , 1991, Science.

[14]  L. Leape,et al.  The appropriateness of use of coronary angiography in New York State. , 1993, JAMA.

[15]  R. Brook,et al.  How coronary angiography is used. Clinical determinants of appropriateness. , 1987, JAMA.

[16]  M. Skolnick,et al.  Statement of the American Society of Clinical Oncology : Genetic testing for cancer susceptibility. Commentaries , 1996 .

[17]  Y. Nakamura,et al.  Screening guidelines and premorbid diagnosis of familial adenomatous polyposis using linkage. , 1991, Gastroenterology.

[18]  G. Petersen,et al.  Gene tests and counseling for colorectal cancer risk: lessons from familial polyposis. , 1995, Journal of the National Cancer Institute. Monographs.

[19]  N. Holtzman Are we ready to screen for inherited susceptibility to cancer? , 1996, Oncology.

[20]  S. Altschul,et al.  Identification of FAP locus genes from chromosome 5q21. , 1991, Science.