Genetic testing for colon cancer susceptibility: Anticipated reactions of patients and challenges to providers

The commercial availability of genetic tests for colon cancer susceptibility is creating new opportunities and challenges for both patients and providers. To provide information useful in the education and counseling of individuals considering genetic testing, we conducted structured interviews with 45 male and female first‐degree relatives of colorectal cancer patients. Fifty‐one percent of respondents indicated that they definitely would want to obtain a genetic test for colon cancer susceptibility when it is available and 31% said that they probably would want to be tested. Interest in genetic testing was significantly higher among persons with less formal education and those with a Catholic religious preference. Motivations for genetic testing included the following: to know if more screening tests are needed, to learn if one's children are at risk and to be reassured. Barriers to testing included concerns about insurance, test accuracy and how one's family would react emotionally. Most participants anticipated that they would become depressed and anxious if they tested positive for a mutation, while many would feel guilty and still worry if they tested negative. Of note, about one‐half of respondents expected that they would decrease their use of screening tests and make fewer attempts to reduce dietary fat if they tested negative. These preliminary results underscore the importance of educating patients about the potential risks, benefits and limitations of genetic testing, with particular emphasis on the possibility of adverse psychological effects and implications for health insurance. The potential for false reassurance following a negative test result should be addressed by emphasizing the residual risks of cancer among non‐carriers of predisposing mutations. © 1996 Wiley‐Liss, Inc.

[1]  R. Rapp Sociocultural differences in the impact of amniocentesis: an anthropological research report. , 1993, Fetal diagnosis and therapy.

[2]  M. Daly,et al.  Attitudes about genetic testing for breast-ovarian cancer susceptibility. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[3]  L. Verbrugge,et al.  Gender and health: an update on hypotheses and evidence. , 1985, Journal of health and social behavior.

[4]  F. Collins,et al.  Genetic counseling for families with inherited susceptibility to breast and ovarian cancer. , 1993, JAMA.

[5]  B. Levin,et al.  Colorectal cancer screening , 1993, Cancer.

[6]  K. Ngo,et al.  Cultural and psychosocial considerations in screening for thalassemia in the Southeast Asian refugee population. , 1993, American journal of medical genetics.

[7]  R. Roos,et al.  DNA-testing for Huntington's disease in The Netherlands: a retrospective study on psychosocial effects. , 1992, American journal of medical genetics.

[8]  R. Croyle,et al.  Psychological issues in genetic testing for breast cancer susceptibility. , 1994, Archives of internal medicine.

[9]  Robin J. Leach,et al.  Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer , 1993, Cell.

[10]  K. Offit,et al.  Quantitating familial cancer risk: a resource for clinical oncologists. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  J. Struewing,et al.  Anticipated uptake and impact of genetic testing in hereditary breast and ovarian cancer families. , 1995, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[12]  D. Craufurd,et al.  UPTAKE OF PRESYMPTOMATIC PREDICTIVE TESTING FOR HUNTINGTON'S DISEASE , 1989, The Lancet.

[13]  C. Lerman,et al.  Interest in genetic testing among first-degree relatives of breast cancer patients. , 1995, American journal of medical genetics.

[14]  M. Sheridan Letter: The handicapped family. , 1975 .

[15]  Mecklin Jp,et al.  Epidemiology of HNPCC. , 1994 .

[16]  R. Croyle,et al.  Interest in genetic testing for colon cancer susceptibility: cognitive and emotional correlates. , 1993, Preventive medicine.

[17]  L. Nsiah-Jefferson Access to reproductive genetic services for low-income women and women of color. , 1993, Fetal diagnosis and therapy.

[18]  M. Hayden,et al.  Predictive testing for Huntington disease in Canada: the experience of those receiving an increased risk. , 1992, American journal of medical genetics.

[19]  G. Lenoir,et al.  DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study. , 1993, Archives of internal medicine.