Skip to main content
Log in

Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review

  • Review Article
  • Published:
Journal of Genetic Counseling

Abstract

Approximately 25 % of individuals undergoing genetic counseling for cancer experiences clinically relevant levels of distress, anxiety and/or depression. However, these general psychological outcomes that are used in many studies do not provide detailed information on the specific psychosocial problems experienced by counselees. The aim of this review was to investigate the specific psychosocial issues encountered by individuals undergoing genetic counseling for cancer, and to identify overarching themes across these issues. A literature search was performed, using four electronic databases (PubMed, PsychInfo, CINAHL and Embase). Papers published between January 2000 and January 2013 were selected using combinations, and related indexing terms of the keywords: ‘genetic counseling’, ‘psychology’ and ‘cancer’. In total, 25 articles met our inclusion criteria. We identified the specific issues addressed by these papers, and used meta-ethnography to identify the following six overarching themes: coping with cancer risk, practical issues, family issues, children-related issues, living with cancer, and emotions. A large overlap in the specific issues and themes was found between these studies, suggesting that research on specific psychosocial problems within genetic counseling has reached a point of saturation. As a next step, efforts should be made to detect and monitor these problems of counselees at an early stage within the genetic counseling process.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  • Aktan-Collan, K. I., Kaariainen, H. A., Kolttola, E. M., Pylvanainen, K., Jarvinen, H. J., Haukkala, A. H., et al. (2011). Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome. Familial Cancer, 10, 43–50.

    Article  PubMed  Google Scholar 

  • Appleton, S., Fry, A., Rees, G., Rush, R., & Cull, A. (2000). Psychosocial effects of living with an increased risk of breast cancer: an exploratory study using telephone focus groups. Psycho-Oncology, 9, 511–521.

    Article  CAS  PubMed  Google Scholar 

  • Atkins, S., Lewin, S., Smith, H., Engel, M., Fretheim, A., & Volmink, J. (2008). Conducting a meta-ethnography of qualitative literature: lessons learnt. BMC Medical Research Methodology, 8, 21.

    Article  PubMed Central  PubMed  Google Scholar 

  • Bakos, A. D., Hutson, S. P., Loud, J. T., Peters, J. A., Giusti, R. M., & Greene, M. H. (2008). BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience. Health Expectations, 11, 220–231.

    Article  PubMed Central  PubMed  Google Scholar 

  • Barnett-Page, E., & Thomas, J. (2009). Methods for the synthesis of qualitative research: a critical review. BMC.Med.Res.Methodol, 9, 59.

    Article  PubMed Central  PubMed  Google Scholar 

  • Bennett, P., Parsons, E., Brain, K., & Hood, K. (2010). Long-term cohort study of women at intermediate risk of familial breast cancer: experiences of living at risk. Psycho-Oncology, 19, 390–398.

    Article  CAS  PubMed  Google Scholar 

  • Bjorvatn, C., Eide, G. E., Hanestad, B. R., Oyen, N., Havik, O. E., Carlsson, A., et al. (2007). Risk perception, worry and satisfaction related to genetic counseling for hereditary cancer. Journal of Genetic Counseling, 16, 211–222.

    Article  PubMed  Google Scholar 

  • Bjorvatn, C., Eide, G. E., Hanestad, B. R., & Havik, O. E. (2008). Anxiety and depression among subjects attending genetic counseling for hereditary cancer. Patient Education and Counseling, 71, 234–243.

    Article  PubMed  Google Scholar 

  • Bonadona, V., Saltel, P., Desseigne, F., Mignotte, H., Saurin, J. C., Wang, Q., et al. (2002). Cancer patients who experienced diagnostic genetic testing for cancer susceptibility: reactions and behavior after the disclosure of a positive test result. Cancer Epidemiology, Biomarkers & Prevention, 11, 97–104.

    Google Scholar 

  • Bradbury, A. R., Patrick-Miller, L., Egleston, B. L., Olopade, O. I., Daly, M. B., Moore, C. W., et al. (2012). When parents disclose BRCA1/2 test results: their communication and perceptions of offspring response. Cancer, 118, 3417–3425.

    Article  PubMed Central  PubMed  Google Scholar 

  • Brady, M. J., Cella, D. F., Mo, F., Bonomi, A. E., Tulsky, D. S., Lloyd, S. R., et al. (1997). Reliability and validity of the Functional Assessment of Cancer Therapy-Breast quality-of-life instrument. Journal of Clinical Oncology, 15, 974–986.

    CAS  PubMed  Google Scholar 

  • Braithwaite, D., Emery, J., Walter, F., Prevost, A. T., & Sutton, S. (2006). Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis. Familial Cancer, 5, 61–75.

    Article  PubMed  Google Scholar 

  • Britten, N., Campbell, R., Pope, C., Donovan, J., Morgan, M., & Pill, R. (2002). Using meta ethnography to synthesise qualitative research: a worked example. Journal of Health Services Research & Policy, 7, 209–215.

    Article  Google Scholar 

  • Broadstock, M., Michie, S., & Marteau, T. (2000). Psychological consequences of predictive genetic testing: a systematic review. European Journal of Human Genetics, 8, 731–738.

    Article  CAS  PubMed  Google Scholar 

  • Butow, P. N., Lobb, E. A., Meiser, B., Barratt, A., & Tucker, K. M. (2003). Psychological outcomes and risk perception after genetic testing and counselling in breast cancer: a systematic review. The Medical Journal of Australia, 178, 77–81.

    PubMed  Google Scholar 

  • Campbell, R., Pound, P., Morgan, M., Daker-White, G., Britten, N., Pill, R., et al. (2011). Evaluating meta-ethnography: systematic analysis and synthesis of qualitative research. Health Technology Assessment, 15, 1–164.

    CAS  PubMed  Google Scholar 

  • Carlsson, C., & Nilbert, M. (2007). Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing. Journal of Genetic Counseling, 16, 811–820.

    Article  CAS  PubMed  Google Scholar 

  • Cheung, E. L., Olson, A. D., Yu, T. M., Han, P. Z., & Beattie, M. S. (2010). Communication of BRCA results and family testing in 1,103 high-risk women. Cancer Epidemiology, Biomarkers & Prevention, 19, 2211–2219.

    Article  CAS  Google Scholar 

  • Claes, E., Evers-Kiebooms, G., Boogaerts, A., Decruyenaere, M., Denayer, L., & Legius, E. (2003). Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. American Journal of Medical Genetics. Part A, 116A, 11–19.

    Article  PubMed  Google Scholar 

  • Coyne, J. C., Benazon, N. R., Gaba, C. G., Calzone, K., & Weber, B. L. (2000). Distress and psychiatric morbidity among women from high-risk breast and ovarian cancer families. Journal of Consulting and Clinical Psychology, 68, 864–874.

    Article  CAS  PubMed  Google Scholar 

  • Crump, R. J., Fitzgerald, R. P., & Legge, M. (2010). ‘Going-to-have-cancerness’: a study of living with increased risk of BRCA1 and BRCA2 mutations for six South Island women. Journal of Primary Health Care, 2, 311–317.

    PubMed  Google Scholar 

  • d’Agincourt-Canning, L. (2006). A gift or a yoke? Women’s and men’s responses to genetic risk information from BRCA1 and BRCA2 testing. Clinical Genetics, 70, 462–472.

    Article  PubMed  Google Scholar 

  • Di Prospero, L. S., Seminsky, M., Honeyford, J., Doan, B., Franssen, E., Meschino, W., et al. (2001). Psychosocial issues following a positive result of genetic testing for BRCA1 and BRCA2 mutations: findings from a focus group and a needs-assessment survey. CMAJ, 164, 1005–1009.

    PubMed Central  PubMed  Google Scholar 

  • Dixon-Woods, M., Agarwal, S., Jones, D., Young, B., & Sutton, A. (2005). Synthesising qualitative and quantitative evidence: a review of possible methods. Journal of Health Services Research & Policy, 10, 45–53.

    Article  Google Scholar 

  • Douglas, H. A., Hamilton, R. J., & Grubs, R. E. (2009). The effect of BRCA gene testing on family relationships: A thematic analysis of qualitative interviews. Journal of Genetic Counseling, 18, 418–435.

    Article  PubMed  Google Scholar 

  • Douma, K. F., Aaronson, N. K., Vasen, H. F., & Bleiker, E. M. (2008). Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature. Psycho-Oncology, 17, 737–745.

    Article  CAS  PubMed  Google Scholar 

  • Douma, K. F., Aaronson, N. K., Vasen, H. F., Gerritsma, M. A., Gundy, C. M., Janssen, E. P., et al. (2010). Psychological distress and use of psychosocial support in familial adenomatous polyposis. Psycho-Oncology, 19, 289–298.

    Article  PubMed  Google Scholar 

  • Duncan, R. E., Gillam, L., Savulescu, J., Williamson, R., Rogers, J. G., & Delatycki, M. B. (2008). “You’re one of us now”: young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP). American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 148C, 47–55.

    Article  PubMed  Google Scholar 

  • Ersig, A. L., Williams, J. K., Hadley, D. W., & Koehly, L. M. (2009). Communication, encouragement, and cancer screening in families with and without mutations for hereditary nonpolyposis colorectal cancer: a pilot study. Genetics in Medicine, 11, 728–734.

    Article  PubMed Central  PubMed  Google Scholar 

  • Esplen, M. J., Madlensky, L., Aronson, M., Rothenmund, H., Gallinger, S., Butler, K., et al. (2007). Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning. Clinical Genetics, 72, 394–401.

    Article  CAS  PubMed  Google Scholar 

  • Frost, C. J., Venne, V., Cunningham, D., & Gerritsen-McKane, R. (2004). Decision making with uncertain information: learning from women in a high risk breast cancer clinic. Journal of Genetic Counseling, 13, 221–236.

    Article  PubMed  Google Scholar 

  • Gallacher, K., Jani, B., Morrison, D., Macdonald, S., Blane, D., Erwin, P., et al. (2013). Qualitative Systematic Reviews of Treatment Burden in Stroke, Heart Failure and Diabetes - Methodological Challenges and Solutions. BMC Medical Research Methodology, 13, 10.

    Article  PubMed Central  PubMed  Google Scholar 

  • Garber, J. E., & Offit, K. (2005). Hereditary cancer predisposition syndromes. Journal of Clinical Oncology, 23, 276–292.

    Article  PubMed  Google Scholar 

  • Hallowell, N., Foster, C., Eeles, R., Ardern-Jones, A., & Watson, M. (2004). Accommodating risk: responses to BRCA1/2 genetic testing of women who have had cancer. Social Science & Medicine, 59, 553–565.

    Article  CAS  Google Scholar 

  • Hallowell, N., Ardern-Jones, A., Eeles, R., Foster, C., Lucassen, A., Moynihan, C., et al. (2005). Communication about genetic testing in families of male BRCA1/2 carriers and non-carriers: patterns, priorities and problems. Clinical Genetics, 67, 492–502.

    Article  CAS  PubMed  Google Scholar 

  • Hallowell, N., Arden-Jones, A., Eeles, R., Foster, C., Lucassen, A., Moynihan, C., et al. (2006). Guilt, blame and responsibility: men’s understanding of their role in the transmission of BRCA1/2 mutations within their family. Sociology of Health & Illness, 28, 969–988.

    Article  Google Scholar 

  • Hamilton, R., & Hurley, K. E. (2010). Conditions and consequences of a BRCA mutation in young, single women of childbearing age. Oncology Nursing Forum, 37, 627–634.

    Article  PubMed  Google Scholar 

  • Hamilton, J. G., Lobel, M., & Moyer, A. (2009a). Emotional distress following genetic testing for hereditary breast and ovarian cancer: a meta-analytic review. Health Psychology, 28, 510–518.

    Article  PubMed Central  PubMed  Google Scholar 

  • Hamilton, R., Williams, J. K., Skirton, H., & Bowers, B. J. (2009b). Living with genetic test results for hereditary breast and ovarian cancer. Journal of Nursing Scholarship, 41, 276–283.

    Article  PubMed  Google Scholar 

  • Kasparian, N. A., Wakefield, C. E., & Meiser, B. (2007). Assessment of psychosocial outcomes in genetic counseling research: an overview of available measurement scales. Journal of Genetic Counseling, 16, 693–712.

    Article  PubMed  Google Scholar 

  • Kasparian, N. A., Meiser, B., Butow, P. N., Simpson, J. M., & Mann, G. J. (2008). Predictors of psychological distress among individuals with a strong family history of malignant melanoma. Clinical Genetics, 73, 121–131.

    Article  CAS  PubMed  Google Scholar 

  • Keller, M., Jost, R., Haunstetter, C. M., Sattel, H., Schroeter, C., Bertsch, U., et al. (2008). Psychosocial outcome following genetic risk counselling for familial colorectal cancer. A comparison of affected patients and family members. Clinical Genetics, 74, 414–424.

    Article  CAS  PubMed  Google Scholar 

  • Kenen, R., Ardern-Jones, A., & Eeles, R. (2003). Living with chronic risk: healthy women with a family history of breast/ovarian cancer. Health, Risk & Society, 5, 315–331.

    Article  Google Scholar 

  • Lammens, C. R., Aaronson, N. K., Wagner, A., Sijmons, R. H., Ausems, M. G., Vriends, A. H., et al. (2010). Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences. Journal of Clinical Oncology, 28, 3008–3014.

    Article  PubMed  Google Scholar 

  • Landsbergen, K. M., Prins, J. B., Brunner, H. G., & Hoogerbrugge, N. (2009a). Genetic testing offered directly after the diagnosis of colorectal cancer: a pilot study on the reactions of patients. Genetic Counseling, 20, 317–325.

    CAS  PubMed  Google Scholar 

  • Landsbergen, K. M., Prins, J. B., Brunner, H. G., Kraaimaat, F. W., & Hoogerbrugge, N. (2009b). Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impact. Familial Cancer, 8, 325–337.

    Article  PubMed Central  PubMed  Google Scholar 

  • Lim, J., Macluran, M., Price, M., Bennett, B., & Butow, P. (2004). Short- and long-term impact of receiving genetic mutation results in women at increased risk for hereditary breast cancer. Journal of Genetic Counseling, 13, 115–133.

    Article  PubMed  Google Scholar 

  • Lindor, N. M., McMaster, M. L., Lindor, C. J., & Greene, M. H. (2008). Concise handbook of familial cancer susceptibility syndromes - second edition. Journal of the National Cancer Institute. Monographs, 1–93.

  • Lodder, L., Frets, P. G., Trijsburg, R. W., Tibben, A., Meijers-Heijboer, E. J., Duivenvoorden, H. J., et al. (2001). Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testing. European Journal of Human Genetics, 9, 492–500.

    Article  CAS  PubMed  Google Scholar 

  • MacDonald, D. J., Sarna, L., Weitzel, J. N., & Ferrell, B. (2010). Women’s perceptions of the personal and family impact of genetic cancer risk assessment: focus group findings. Journal of Genetic Counseling, 19, 148–160.

    Article  PubMed  Google Scholar 

  • Maheu, C. (2009). Implications of living with a strong family history of breast cancer. Canadian Journal of Nursing Research, 41, 100–112.

    PubMed  Google Scholar 

  • McCann, S., MacAuley, D., Barnett, Y., Bunting, B., Bradley, A., Jeffers, L., et al. (2009). Family communication, genetic testing and colonoscopy screening in hereditary non-polyposis colon cancer: a qualitative study. Psycho-Oncology, 18, 1208–1215.

    Article  PubMed  Google Scholar 

  • Meiser, B. (2005). Psychological impact of genetic testing for cancer susceptibility: an update of the literature. Psycho-Oncology, 14, 1060–1074.

    Article  PubMed  Google Scholar 

  • Meiser, B., Butow, P., Friedlander, M., Barratt, A., Schnieden, V., Watson, M., et al. (2002). Psychological impact of genetic testing in women from high-risk breast cancer families. European Journal of Cancer, 38, 2025–2031.

    Article  CAS  PubMed  Google Scholar 

  • Meiser, B., Tucker, K., Friedlander, M., Barlow-Stewart, K., Lobb, E., Saunders, C., et al. (2008). Genetic counselling and testing for inherited gene mutations in newly diagnosed patients with breast cancer: a review of the existing literature and a proposed research agenda. Breast Cancer Research, 10, 216.

    Article  PubMed Central  PubMed  Google Scholar 

  • Mellon, S., Gold, R., Janisse, J., Cichon, M., Tainsky, M. A., Simon, M. S., et al. (2008). Risk perception and cancer worries in families at increased risk of familial breast/ovarian cancer. Psycho-Oncology, 17, 756–766.

    Article  PubMed Central  PubMed  Google Scholar 

  • Mendes, A. F., Santos, T. A., & Sousa, L. (2011). Experiencing genetic counselling for hereditary cancers: the client’s perspective. European Journal of Cancer Care (Engl), 20, 204–211.

    Article  CAS  Google Scholar 

  • Mireskandari, S., Sangster, J., Meiser, B., Thewes, B., Groombridge, C., Spigelman, A., et al. (2009). Psychosocial impact of familial adenomatous polyposis on young adults: a qualitative study. Journal of Genetic Counseling, 18, 409–417.

    Article  PubMed  Google Scholar 

  • Noblit, G. W., & Hare, R. D. (1988). Meta-Ethnography: Synthesizing Qualitative Studies. London: Sage.

    Google Scholar 

  • Pasacreta, J. V. (2003). Psychosocial issues associated with genetic testing for breast and ovarian cancer risk: an integrative review. Cancer Investigation, 21, 588–623.

    Article  PubMed  Google Scholar 

  • Patenaude, A. F., Dorval, M., DiGianni, L. S., Schneider, K. A., Chittenden, A., & Garber, J. E. (2006). Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tell. Journal of Clinical Oncology, 24, 700–706.

    Article  PubMed  Google Scholar 

  • Payne, K., Nicholls, S., McAllister, M., Macleod, R., Donnai, D., & Davies, L. M. (2008). Outcome measurement in clinical genetics services: a systematic review of validated measures. Value in Health, 11, 497–508.

    Article  PubMed  Google Scholar 

  • Pound, P., Britten, N., Morgan, M., Yardley, L., Pope, C., Daker-White, G., et al. (2005). Resisting medicines: a synthesis of qualitative studies of medicine taking. Social Science & Medicine, 61, 133–155.

    Article  Google Scholar 

  • Resta, R., Biesecker, B. B., Bennett, R. L., Blum, S., Hahn, S. E., Strecker, M. N., et al. (2006). A new definition of Genetic Counseling: National Society of Genetic Counselors’ Task Force report. Journal of Genetic Counseling, 15, 77–83.

    Article  PubMed  Google Scholar 

  • Riley, B. D., Culver, J. O., Skrzynia, C., Senter, L. A., Peters, J. A., Costalas, J. W., et al. (2012). Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling, 21, 151–161.

    Article  PubMed  Google Scholar 

  • Ring, N., Jepson, R., & Ritchie, K. (2011). Methods of synthesizing qualitative research studies for health technology assessment. International Journal of Technology Assessment in Health Care, 27, 384–390.

    Article  PubMed  Google Scholar 

  • Schlich-Bakker, K. J., ten Kroode, H. F., & Ausems, M. G. (2006a). A literature review of the psychological impact of genetic testing on breast cancer patients. Patient Education and Counseling, 62, 13–20.

    Article  PubMed  Google Scholar 

  • Schlich-Bakker, K. J., Warlam-Rodenhuis, C. C., van Echtelt, J., van den Bout, J., Ausems, M. G., & ten Kroode, H. F. (2006b). Short term psychological distress in patients actively approached for genetic counselling after diagnosis of breast cancer. European Journal of Cancer, 42, 2722–2728.

    Article  PubMed  Google Scholar 

  • Sprangers, M. A., te Velde, A., & Aaronson, N. K. (1999). The construction and testing of the EORTC colorectal cancer-specific quality of life questionnaire module (QLQ-CR38). European Organization for Research and Treatment of Cancer Study Group on Quality of Life. European Journal of Cancer, 35, 238–247.

    Article  CAS  PubMed  Google Scholar 

  • Street, R. L., Jr., Makoul, G., Arora, N. K., & Epstein, R. M. (2009). How does communication heal? Pathways linking clinician-patient communication to health outcomes. Patient Education and Counseling, 74, 295–301.

    Article  PubMed  Google Scholar 

  • Stromsvik, N., Raheim, M., Oyen, N., & Gjengedal, E. (2009). Men in the women’s world of hereditary breast and ovarian cancer–a systematic review. Familial Cancer, 8, 221–229.

    Article  PubMed  Google Scholar 

  • Stromsvik, N., Raheim, M., Oyen, N., Engebretsen, L. F., & Gjengedal, E. (2010). Stigmatization and male identity: Norwegian males’ experience after identification as BRCA1/2 mutation carriers. Journal of Genetic Counseling, 19, 360–370.

    Article  PubMed  Google Scholar 

  • Stromsvik, N., Raheim, M., & Gjengedal, E. (2011). Cancer worry among Norwegian male BRCA1/2 mutation carriers. Familial Cancer, 10, 597–603.

    Article  PubMed Central  PubMed  Google Scholar 

  • Stroup, A. M., & Smith, K. R. (2007). Familial effects of BRCA1 genetic mutation testing: changes in perceived family functioning. Cancer Epidemiology, Biomarkers & Prevention, 16, 135–141.

    Article  CAS  Google Scholar 

  • Tercyak, K. P., Peshkin, B. N., DeMarco, T. A., Brogan, B. M., & Lerman, C. (2002). Parent–child factors and their effect on communicating BRCA1/2 test results to children. Patient Education and Counseling, 47, 145–153.

    Article  PubMed  Google Scholar 

  • Tercyak, K. P., Peshkin, B. N., DeMarco, T. A., Patenaude, A. F., Schneider, K. A., Garber, J. E., et al. (2007). Information needs of mothers regarding communicating BRCA1/2 cancer genetic test results to their children. Genetic Testing, 11, 249–255.

    Article  PubMed Central  PubMed  Google Scholar 

  • Trepanier, A., Ahrens, M., McKinnon, W., Peters, J., Stopfer, J., Grumet, S. C., et al. (2004). Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. Journal of Genetic Counseling, 13, 83–114.

    Article  PubMed  Google Scholar 

  • Turner-Cobb, J. M., Bloor, L. E., Whittemore, A. S., West, D., & Spiegel, D. (2006). Disengagement and social support moderate distress among women with a family history of breast cancer. The Breast Journal, 12, 7–15.

    Article  PubMed  Google Scholar 

  • Vadaparampil, S. T., Miree, C. A., Wilson, C., & Jacobsen, P. B. (2006). Psychosocial and behavioral impact of genetic counseling and testing. Breast Disease, 27, 97–108.

    PubMed  Google Scholar 

  • Vadaparampil, S. T., Quinn, G. P., Brzosowicz, J., & Miree, C. A. (2008). Experiences of genetic counseling for BRCA1/2 among recently diagnosed breast cancer patients: a qualitative inquiry. Journal of Psychosocial Oncology, 26, 33–52.

    Article  PubMed  Google Scholar 

  • Vos, J., van Asperen, C. J., Oosterwijk, J. C., Menko, F. H., Collee, M . J., Garcia, E. G. et al. (2013). The counselees’ self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters. Psycho-Oncology, 22, 902–910.

  • Wagner Costalas, J., Itzen, M., Malick, J., Babb, J. S., Bove, B., Godwin, A. K., et al. (2003). Communication of BRCA1 and BRCA2 results to at-risk relatives: a cancer risk assessment program’s experience. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 119C, 11–18.

    Article  PubMed  Google Scholar 

  • Walter, F. M., Emery, J., Braithwaite, D., & Marteau, T. M. (2004). Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research. Annals of Family Medicine, 2, 583–594.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgement

This study is supported financially by the Dutch Cancer Society (grant number NKI 2008–4016).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Eveline MA Bleiker.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eijzenga, W., Hahn, D.E., Aaronson, N.K. et al. Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review. J Genet Counsel 23, 133–146 (2014). https://doi.org/10.1007/s10897-013-9649-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10897-013-9649-4

Keywords

Navigation