Skip to main content
Top
Published in: Journal of Genetic Counseling 4/2009

01-08-2009 | Original Research

The Effectiveness of Family History Questionnaires in Cancer Genetic Counseling

Authors: Susan Randall Armel, Jeanna McCuaig, Amy Finch, Rochelle Demsky, Tony Panzarella, Joan Murphy, Barry Rosen

Published in: Journal of Genetic Counseling | Issue 4/2009

Login to get access

Abstract

The number of individuals receiving genetic counseling for hereditary breast and ovarian cancer syndrome has steadily risen. To triage patients for genetic counseling and to help reduce the amount of time needed by a genetic counselor in direct patient contact, many clinics have implemented the use of family history questionnaires. Although such questionnaires are widely used, scant literature exists evaluating their effectiveness. This article explores the extent to which family history questionnaires are being used in Ontario and addresses the utility of such questionnaires in one familial cancer clinic. By comparing the pedigrees created from questionnaires to those updated during genetic counseling, the accuracy and effectiveness of the questionnaires was explored. Of 121 families recruited into the study, 12% acquired changes to their pedigree that led to a revised probability estimate for having a BRCA1 or BRCA2 mutation and 5% acquired changes that altered their eligibility for genetic testing. No statistically significant difference existed between the eligibility for genetic testing prior to and post counseling. This suggests that family history questionnaires can be effective at obtaining a family history and accurately assessing eligibility for genetic testing. Based on the variables that were significantly associated with a change in probability estimate, we further present recommendations for improving the clarity of such questionnaires and therefore the ease of use by patients.
Appendix
Available only for authorised users
Literature
go back to reference Antoniou, A., Pharoah, P. D., Narod, S., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. American Journal of Human Genetics, 72, 1117–1130. doi:https://doi.org/10.1086/375033.CrossRef Antoniou, A., Pharoah, P. D., Narod, S., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. American Journal of Human Genetics, 72, 1117–1130. doi:https://​doi.​org/​10.​1086/​375033.CrossRef
go back to reference Berry, D. A., Iversen, E. S,. Jr, Gudbjartsson, D. F., Hiller, E. H., Garber, J. E., Peshkin, B. N., et al. (2002). BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. Journal of Clinical Oncology, 20(11), 2701–2712. doi:https://doi.org/10.1200/JCO.2002.05.121.CrossRef Berry, D. A., Iversen, E. S,. Jr, Gudbjartsson, D. F., Hiller, E. H., Garber, J. E., Peshkin, B. N., et al. (2002). BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. Journal of Clinical Oncology, 20(11), 2701–2712. doi:https://​doi.​org/​10.​1200/​JCO.​2002.​05.​121.CrossRef
go back to reference Brener, D., Schulz, C., Schluger, A., & Offit, K. (1996). A self-administered family history questionnaire (FHQ) utilized in an outpatient setting to assess cancer risk. American Journal of Human Genetics, 59, A333. Brener, D., Schulz, C., Schluger, A., & Offit, K. (1996). A self-administered family history questionnaire (FHQ) utilized in an outpatient setting to assess cancer risk. American Journal of Human Genetics, 59, A333.
go back to reference FamyGenetix Ltd. (2001). Cyrillic 3. Oxford: UK. FamyGenetix Ltd. (2001). Cyrillic 3. Oxford: UK.
go back to reference Hallowell, N., Murton, F., Statham, H., Green, J. M., & Richards, M. P. (1997). Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview, and observational study. BMJ (Clinical Research Ed), 281, 7076–283. Hallowell, N., Murton, F., Statham, H., Green, J. M., & Richards, M. P. (1997). Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview, and observational study. BMJ (Clinical Research Ed), 281, 7076–283.
go back to reference NCIC. (2007). Canadian Cancer Statistics 2007. Toronto: Canada. NCIC. (2007). Canadian Cancer Statistics 2007. Toronto: Canada.
go back to reference Risch, H. A., McLaughlin, J. R., Cole, D. E., Rosen, B., Bradley, L., Kwan, E., et al. (2001). Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. American Journal of Human Genetics, 68(3), 700–710. doi:https://doi.org/10.1086/318787.CrossRef Risch, H. A., McLaughlin, J. R., Cole, D. E., Rosen, B., Bradley, L., Kwan, E., et al. (2001). Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. American Journal of Human Genetics, 68(3), 700–710. doi:https://​doi.​org/​10.​1086/​318787.CrossRef
go back to reference Risch, H. A., McLaughlin, J. R., Cole, D. E., Rosen, B., Bradley, L., Fan, I., et al. (2006). Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. Journal of the National Cancer Institute, 98(23), 1694–1706.CrossRef Risch, H. A., McLaughlin, J. R., Cole, D. E., Rosen, B., Bradley, L., Fan, I., et al. (2006). Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. Journal of the National Cancer Institute, 98(23), 1694–1706.CrossRef
go back to reference Satagopan, J. M., Offit, K., Foulkes, W., Robson, M. E., Wacholder, S., Eng, C. M., et al. (2001). The lifetime risks of breast cancer in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations. Cancer Epidemiology, Biomarkers & Prevention, 10(5), 467–473. Satagopan, J. M., Offit, K., Foulkes, W., Robson, M. E., Wacholder, S., Eng, C. M., et al. (2001). The lifetime risks of breast cancer in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations. Cancer Epidemiology, Biomarkers & Prevention, 10(5), 467–473.
go back to reference Whittemore, A. S., Gong, G., & Itnyre, J. (1997). Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: results from three U.S. population-based case-control studies of ovarian cancer. American Journal of Human Genetics, 60(3), 496–504.PubMedPubMedCentral Whittemore, A. S., Gong, G., & Itnyre, J. (1997). Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: results from three U.S. population-based case-control studies of ovarian cancer. American Journal of Human Genetics, 60(3), 496–504.PubMedPubMedCentral
Metadata
Title
The Effectiveness of Family History Questionnaires in Cancer Genetic Counseling
Authors
Susan Randall Armel
Jeanna McCuaig
Amy Finch
Rochelle Demsky
Tony Panzarella
Joan Murphy
Barry Rosen
Publication date
01-08-2009
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 4/2009
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-009-9228-x

Other articles of this Issue 4/2009

Journal of Genetic Counseling 4/2009 Go to the issue