Skip to main content
Top
Published in: Journal of Genetic Counseling 3/2013

01-06-2013 | Original Research

Acceptance of Genetic Counseling and Testing in a Hospital-Based Series of Patients with Gynecological Cancer

Authors: Nicky Dekker, Eleonora B. L. van Dorst, Rob B. van der Luijt, Marielle E. van Gijn, Marc van Tuil, Johan A. Offerhaus, Margreet G. E. M. Ausems

Published in: Journal of Genetic Counseling | Issue 3/2013

Login to get access

Abstract

Referral of patients with endometrial (EC) and/or ovarian cancer (OC) for genetic counseling is based on age at diagnosis and family history. Many patients with hereditary cancers are missed by following this strategy. We determined acceptance and mutation detection rate of offering genetic counseling and testing to unselected EC and OC patients. Therefore, in 2007, EC and OC patients were invited for genetic counseling and testing. Patients were asked for their reasons to accept or decline. Nineteen out of fifty-two EC patients (36 %) and twenty-two out of thirty-five OC patients (63 %) accepted genetic counseling, mainly to receive risk assessment for themselves and relatives. Counseling was declined mainly because patients did not want more tests or had no relatives for whom it was relevant. Eighteen out of nineteen EC patients (95 %) and twenty out of twenty-two OC patients (91 %) underwent genetic testing. One EC patient carried an MSH6 mutation (mutation detection rate: 6 %). BRCA1/2 mutations were found in two out of twenty OC patients (10 %). Eleven patients (29 %) received surveillance recommendations for themselves and their relatives. Finally, family history recorded by the gynecologist was compared to that taken by the clinical geneticist. Gynecologists reported family history in ten out of forty-one participants (24 %). In conclusion, genetic counseling and testing are acceptable to patients with OC and/or EC. The 10 % BRCA1/2 mutation detection rate and underreporting of family history by gynecologists warrant referral for genetic counseling for all OC patients, followed by BRCA1/2 testing if indicated. We recommend that microsatellite instability and immunohistochemical analysis be performed in all EC patients, followed by genetic counseling if appropriate. These strategies will lead to better cancer prevention in gynecological cancer patients and their relatives.
Literature
go back to reference Aarnio, M., Sankila, R., Pukkala, E., Salovaara, R., Aaltonen, L. A., de la Chapelle, A., et al. (1999). Cancer risks in mutation carriers of DNA-mismatch-repair genes. International Journal of Cancer, 81(2), 214–218.CrossRef Aarnio, M., Sankila, R., Pukkala, E., Salovaara, R., Aaltonen, L. A., de la Chapelle, A., et al. (1999). Cancer risks in mutation carriers of DNA-mismatch-repair genes. International Journal of Cancer, 81(2), 214–218.CrossRef
go back to reference American Society of Clinical Oncology. (2003). Statement of the American Society of Clinical Oncology policy statement update: Genetic Testing for Cancer susceptibility. Journal of Clinical Oncology, 21(12), 2397–2406.CrossRef American Society of Clinical Oncology. (2003). Statement of the American Society of Clinical Oncology policy statement update: Genetic Testing for Cancer susceptibility. Journal of Clinical Oncology, 21(12), 2397–2406.CrossRef
go back to reference Armstrong, K., Calzone, K., Stopfer, J., Fitzgerald, G., Coyne, J., & Weber, B. (2000). Factors associated with decisions about clinical BRCA1/2 testing. Cancer Epidemiology, Biomarkers and Prevention, 9(11), 1251–1254.PubMed Armstrong, K., Calzone, K., Stopfer, J., Fitzgerald, G., Coyne, J., & Weber, B. (2000). Factors associated with decisions about clinical BRCA1/2 testing. Cancer Epidemiology, Biomarkers and Prevention, 9(11), 1251–1254.PubMed
go back to reference Auranen, A., & Joutsiniemi, T. (2011). A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families. ACTA Obstetricia et Gynecologica Scandinavica, 90(5), 437–444.PubMedCrossRef Auranen, A., & Joutsiniemi, T. (2011). A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families. ACTA Obstetricia et Gynecologica Scandinavica, 90(5), 437–444.PubMedCrossRef
go back to reference Backes, F. J., Hampel, H., Backes, K. A., Vaccarello, L., Lewandowski, G., Bell, J. A., et al. (2009). Are prediction models for Lynch syndrome valid for probands with endometrial cancer? Familial Cancer, 8(4), 483–487.PubMedCrossRef Backes, F. J., Hampel, H., Backes, K. A., Vaccarello, L., Lewandowski, G., Bell, J. A., et al. (2009). Are prediction models for Lynch syndrome valid for probands with endometrial cancer? Familial Cancer, 8(4), 483–487.PubMedCrossRef
go back to reference Backes, F. J., Mitchell, E., Hampel, H., & Cohn, D. E. (2011). Endometrial cancer patients and compliance with genetic counseling: room for improvement. Gynecologic Oncology, 123(3), 532–536.PubMedCrossRef Backes, F. J., Mitchell, E., Hampel, H., & Cohn, D. E. (2011). Endometrial cancer patients and compliance with genetic counseling: room for improvement. Gynecologic Oncology, 123(3), 532–536.PubMedCrossRef
go back to reference Baer, H. J., Brawarsky, P., Murray, M. F., & Haas, J. S. (2010). Familial risk of cancer and knowledge and use of genetic testing. Journal of General Internal Medicine, 25(7), 717–724.PubMedCrossRef Baer, H. J., Brawarsky, P., Murray, M. F., & Haas, J. S. (2010). Familial risk of cancer and knowledge and use of genetic testing. Journal of General Internal Medicine, 25(7), 717–724.PubMedCrossRef
go back to reference Balmaña, J., Diez, O., Rubio, I., Castiglione, M., & ESMO Guidelines Working Group. (2010). BRCA in breast cancer: ESMO Clinical Practice Guidelines. Annals of Oncology, 21(Suppl 5), v20–22.PubMedCrossRef Balmaña, J., Diez, O., Rubio, I., Castiglione, M., & ESMO Guidelines Working Group. (2010). BRCA in breast cancer: ESMO Clinical Practice Guidelines. Annals of Oncology, 21(Suppl 5), v20–22.PubMedCrossRef
go back to reference Banno, K., Susumu, N., Yanokura, M., Hirao, T., Iwata, T., Hirasawa, A., et al. (2004). Association of HNPCC and endometrial cancers. International Journal of Clinical Oncology, 9(4), 262–269.PubMedCrossRef Banno, K., Susumu, N., Yanokura, M., Hirao, T., Iwata, T., Hirasawa, A., et al. (2004). Association of HNPCC and endometrial cancers. International Journal of Clinical Oncology, 9(4), 262–269.PubMedCrossRef
go back to reference Bonadona, V., Bonaïti, B., Olschwang, S., Grandjouan, S., Huiart, L., Longy, M., et al. (2011). Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. Journal of the American Medical Association, 305(22), 2304–2310.PubMedCrossRef Bonadona, V., Bonaïti, B., Olschwang, S., Grandjouan, S., Huiart, L., Longy, M., et al. (2011). Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. Journal of the American Medical Association, 305(22), 2304–2310.PubMedCrossRef
go back to reference Brozek, I., Ochman, K., Debniak, J., Morzuch, L., Ratajska, M., Stepnowska, M., et al. (2008). High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecologic Oncology, 108(2), 433–437.PubMedCrossRef Brozek, I., Ochman, K., Debniak, J., Morzuch, L., Ratajska, M., Stepnowska, M., et al. (2008). High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecologic Oncology, 108(2), 433–437.PubMedCrossRef
go back to reference Devlin, L., Graham, C. A., Price, J. H., & Morrison, P. J. (2008). Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts. Ulster Medical Journal, 77(1), 25–30.PubMed Devlin, L., Graham, C. A., Price, J. H., & Morrison, P. J. (2008). Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts. Ulster Medical Journal, 77(1), 25–30.PubMed
go back to reference Domanska, K., Carlsson, C., Bendahl, P. O., & Nilbert, M. (2009). Knowledge about hereditary non-polyposis colorectal cancer; mutation carriers and physicians at equal levels. BMC Medical Genetics, 10, 30.PubMedCrossRef Domanska, K., Carlsson, C., Bendahl, P. O., & Nilbert, M. (2009). Knowledge about hereditary non-polyposis colorectal cancer; mutation carriers and physicians at equal levels. BMC Medical Genetics, 10, 30.PubMedCrossRef
go back to reference Dove-Edwin, I., Sasieni, P., Adams, J., & Thomas, H. J. (2005). Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study. British Medical Journal, 331(7524), 1047.PubMedCrossRef Dove-Edwin, I., Sasieni, P., Adams, J., & Thomas, H. J. (2005). Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study. British Medical Journal, 331(7524), 1047.PubMedCrossRef
go back to reference Drew, Y., & Calvert, H. (2008). The potential of PARP inhibitors in genetic breast and ovarian cancers. Annals of the New York Academy of Sciences, 1138, 136–145.PubMedCrossRef Drew, Y., & Calvert, H. (2008). The potential of PARP inhibitors in genetic breast and ovarian cancers. Annals of the New York Academy of Sciences, 1138, 136–145.PubMedCrossRef
go back to reference Frank, T. S., Deffenbaugh, A. M., Reid, J. E., Hulick, M., Ward, B. E., Lingenfelter, B., et al. (2002). Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. Journal of Clinical Oncology, 20(6), 1480–1490.PubMedCrossRef Frank, T. S., Deffenbaugh, A. M., Reid, J. E., Hulick, M., Ward, B. E., Lingenfelter, B., et al. (2002). Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. Journal of Clinical Oncology, 20(6), 1480–1490.PubMedCrossRef
go back to reference Garg, K., & Soslow, R. A. (2009). Lynch syndrome (hereditary non-polyposis colorectal cancer) and endometrial carcinoma. Journal of Clinical Pathology, 62(8), 679–684.PubMedCrossRef Garg, K., & Soslow, R. A. (2009). Lynch syndrome (hereditary non-polyposis colorectal cancer) and endometrial carcinoma. Journal of Clinical Pathology, 62(8), 679–684.PubMedCrossRef
go back to reference Geer, K. P., Ropka, M. E., Cohn, W. F., Jones, S. M., & Miesfeldt, S. (2001). Factors influencing patients’ decisions to decline cancer genetic counseling services. Journal of Genetic Counseling, 10(1), 25–40.PubMedCrossRef Geer, K. P., Ropka, M. E., Cohn, W. F., Jones, S. M., & Miesfeldt, S. (2001). Factors influencing patients’ decisions to decline cancer genetic counseling services. Journal of Genetic Counseling, 10(1), 25–40.PubMedCrossRef
go back to reference Godard, B., Pratte, A., Dumont, M., Simard-Lebrun, A., & Simard, J. (2007). Factors associated with an individual’s decision to withdraw from genetic testing for breast and ovarian cancer susceptibility: implications for counseling. Genetic Testing, 11(1), 45–54.PubMedCrossRef Godard, B., Pratte, A., Dumont, M., Simard-Lebrun, A., & Simard, J. (2007). Factors associated with an individual’s decision to withdraw from genetic testing for breast and ovarian cancer susceptibility: implications for counseling. Genetic Testing, 11(1), 45–54.PubMedCrossRef
go back to reference Goodfellow, P. J., Buttin, B. M., Herzog, T. J., Rader, J. S., Gibb, R. K., Swisher, E., et al. (2003). Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. Proceedings of the National Academy of the Sciences, 100(10), 5908–5913.CrossRef Goodfellow, P. J., Buttin, B. M., Herzog, T. J., Rader, J. S., Gibb, R. K., Swisher, E., et al. (2003). Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. Proceedings of the National Academy of the Sciences, 100(10), 5908–5913.CrossRef
go back to reference Hampel, H., Frankel, W., Panescu, J., Lockman, J., Sotamaa, K., Fix, D., et al. (2006). Screening for Lynch syndrome (Hereditary Nonpolyposis Colorectal Cancer) among endometrial cancer patients. Cancer Research, 66(15), 7810–7817.PubMedCrossRef Hampel, H., Frankel, W., Panescu, J., Lockman, J., Sotamaa, K., Fix, D., et al. (2006). Screening for Lynch syndrome (Hereditary Nonpolyposis Colorectal Cancer) among endometrial cancer patients. Cancer Research, 66(15), 7810–7817.PubMedCrossRef
go back to reference Hes, F. J. (2008). Lynch syndrome: still not a familiar picture. World Journal of Surgical Oncology, 6, 21.PubMedCrossRef Hes, F. J. (2008). Lynch syndrome: still not a familiar picture. World Journal of Surgical Oncology, 6, 21.PubMedCrossRef
go back to reference Hoogerbrugge, N. (2010). Recognizing hereditary cancer: new simple referral criteria for solid cancers. Netherlands Journal of Oncology, 7, 330–337. Hoogerbrugge, N. (2010). Recognizing hereditary cancer: new simple referral criteria for solid cancers. Netherlands Journal of Oncology, 7, 330–337.
go back to reference Jacobi, C. E., Van Ierland, Y., Van Asperen, C. J., Hallensleben, E., Devilee, P., et al. (2007). Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort. Genetics in Medicine, 9(3), 173–179.PubMedCrossRef Jacobi, C. E., Van Ierland, Y., Van Asperen, C. J., Hallensleben, E., Devilee, P., et al. (2007). Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort. Genetics in Medicine, 9(3), 173–179.PubMedCrossRef
go back to reference Järvinen, H. J., Aarnio, M., Mustonen, H., Aktan-Collan, K., Aaltonen, L. A., Peltomäki, P., et al. (2000). Controlled 15-year trial on screening for colorectal cancer in families with hereditary non-polyposis colorectal cancer. Gastroenterology, 118(5), 829–834.PubMedCrossRef Järvinen, H. J., Aarnio, M., Mustonen, H., Aktan-Collan, K., Aaltonen, L. A., Peltomäki, P., et al. (2000). Controlled 15-year trial on screening for colorectal cancer in families with hereditary non-polyposis colorectal cancer. Gastroenterology, 118(5), 829–834.PubMedCrossRef
go back to reference Julian-Reynier, C., Eisinger, F., Chabal, F., Aurran, Y., Bignon, Y. J., Noguès, C., et al. (1998). Cancer genetic clinics: why do women who already have cancer attend? European Journal of Cancer, 34(10), 1549–1553.PubMedCrossRef Julian-Reynier, C., Eisinger, F., Chabal, F., Aurran, Y., Bignon, Y. J., Noguès, C., et al. (1998). Cancer genetic clinics: why do women who already have cancer attend? European Journal of Cancer, 34(10), 1549–1553.PubMedCrossRef
go back to reference Khoo, U. S., Ngan, H. Y., Cheung, A. N., Chan, K. Y., Lu, J., Chan, V. W., et al. (2000). Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations. Human Mutation, 16(1), 88–89.PubMedCrossRef Khoo, U. S., Ngan, H. Y., Cheung, A. N., Chan, K. Y., Lu, J., Chan, V. W., et al. (2000). Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations. Human Mutation, 16(1), 88–89.PubMedCrossRef
go back to reference Khoo, U. S., Chan, K. Y., Cheung, A. N., Xue, W. C., Shen, D. H., Fung, K. Y., et al. (2002). Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population. Human Mutation, 19(3), 307–308.PubMedCrossRef Khoo, U. S., Chan, K. Y., Cheung, A. N., Xue, W. C., Shen, D. H., Fung, K. Y., et al. (2002). Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population. Human Mutation, 19(3), 307–308.PubMedCrossRef
go back to reference Lacour, R. A., Daniels, M. S., Westin, S. N., Meyer, L. A., Burke, C. C., Burns, K. A., et al. (2008). What women with ovarian cancer think and know about genetic testing. Gynecologic Oncology, 111(1), 132–136.PubMedCrossRef Lacour, R. A., Daniels, M. S., Westin, S. N., Meyer, L. A., Burke, C. C., Burns, K. A., et al. (2008). What women with ovarian cancer think and know about genetic testing. Gynecologic Oncology, 111(1), 132–136.PubMedCrossRef
go back to reference Leenen, C. H., Van Lier, M. G., Van Doorn, H. C., Van Leerdam, M. E., Kooi, S. G., De Waard, J., et al. (2012). Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years. Gynecologic Oncology, 125(2), 414–420.PubMedCrossRef Leenen, C. H., Van Lier, M. G., Van Doorn, H. C., Van Leerdam, M. E., Kooi, S. G., De Waard, J., et al. (2012). Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years. Gynecologic Oncology, 125(2), 414–420.PubMedCrossRef
go back to reference Liede, A., Malik, I. A., Aziz, Z., De los Rios, P., Kwan, E., & Narod, S. A. (2002). Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan. American Journal of Human Genetics, 71(3), 595–606.PubMedCrossRef Liede, A., Malik, I. A., Aziz, Z., De los Rios, P., Kwan, E., & Narod, S. A. (2002). Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan. American Journal of Human Genetics, 71(3), 595–606.PubMedCrossRef
go back to reference Ligtenberg, M. J., Kuiper, R. P., Chan, T. L., Goossens, M., Hebeda, K. M., Voorendt, M., et al. (2009). Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. Nature Genetics, 41(1), 112–117.PubMedCrossRef Ligtenberg, M. J., Kuiper, R. P., Chan, T. L., Goossens, M., Hebeda, K. M., Voorendt, M., et al. (2009). Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. Nature Genetics, 41(1), 112–117.PubMedCrossRef
go back to reference Lim, M. C., Seo, S. S., Kang, S., Seong, M. W., Lee, B. Y., & Park, S. Y. (2010). Hereditary non-polyposis colorectal cancer/Lynch syndrome in Korean patients with endometrial cancer. Japanese Journal of Clinical Oncology, 40(12), 1121–1127.PubMedCrossRef Lim, M. C., Seo, S. S., Kang, S., Seong, M. W., Lee, B. Y., & Park, S. Y. (2010). Hereditary non-polyposis colorectal cancer/Lynch syndrome in Korean patients with endometrial cancer. Japanese Journal of Clinical Oncology, 40(12), 1121–1127.PubMedCrossRef
go back to reference Long, K. C., & Kauff, N. D. (2011). Hereditary ovarian cancer: recent molecular insights and their impact on screening strategies. Current Opinion in Oncology, 23(5), 526–530.PubMedCrossRef Long, K. C., & Kauff, N. D. (2011). Hereditary ovarian cancer: recent molecular insights and their impact on screening strategies. Current Opinion in Oncology, 23(5), 526–530.PubMedCrossRef
go back to reference Lynch, H. T., Watson, P., Tinley, S., Snyder, C., Durham, C., Lynch, J., et al. (1999). An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer. Cancer Genetica and Cytogenetics, 109(2), 91–98.CrossRef Lynch, H. T., Watson, P., Tinley, S., Snyder, C., Durham, C., Lynch, J., et al. (1999). An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer. Cancer Genetica and Cytogenetics, 109(2), 91–98.CrossRef
go back to reference Majdak, E. J., De Bock, G. H., Brozek, I., Perkowska, M., Ochman, K., Debniak, J., et al. (2005). Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases – preliminary report. European Journal of Cancer, 41(1), 143–150.PubMedCrossRef Majdak, E. J., De Bock, G. H., Brozek, I., Perkowska, M., Ochman, K., Debniak, J., et al. (2005). Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases – preliminary report. European Journal of Cancer, 41(1), 143–150.PubMedCrossRef
go back to reference Malander, S., Ridderheim, M., Måsbäck, A., Loman, N., Kristoffersson, U., Olsson, H., et al. (2004). One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden. European Journal of Cancer, 40(3), 422–428.PubMedCrossRef Malander, S., Ridderheim, M., Måsbäck, A., Loman, N., Kristoffersson, U., Olsson, H., et al. (2004). One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden. European Journal of Cancer, 40(3), 422–428.PubMedCrossRef
go back to reference Manders, P., Spruijt, L., Kets, C. M., Willems, H. W., Bodmer, D., Hebeda, K. M., et al. (2011). Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. European Journal of Cancer, 47(9), 1407–1413.PubMedCrossRef Manders, P., Spruijt, L., Kets, C. M., Willems, H. W., Bodmer, D., Hebeda, K. M., et al. (2011). Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. European Journal of Cancer, 47(9), 1407–1413.PubMedCrossRef
go back to reference Meyer, L. A., Anderson, M. E., Lacour, R. A., Suri, A., Daniels, M. S., Urbauer, D. L., et al. (2010). Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities. Obstetrics and Gynecology, 115(5), 945–952.PubMedCrossRef Meyer, L. A., Anderson, M. E., Lacour, R. A., Suri, A., Daniels, M. S., Urbauer, D. L., et al. (2010). Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities. Obstetrics and Gynecology, 115(5), 945–952.PubMedCrossRef
go back to reference Murphy, M. A., & Wentzensen, N. (2011). Frequency of mismatch repair deficiency in ovarian cancer: a systematic review. International Journal of Cancer, 129, 1914–1922.CrossRef Murphy, M. A., & Wentzensen, N. (2011). Frequency of mismatch repair deficiency in ovarian cancer: a systematic review. International Journal of Cancer, 129, 1914–1922.CrossRef
go back to reference Netherlands Foundation for the Detection of Hereditary Tumours (STOET) and Dutch Society for Clinical Genetics (VKGN). (2005, 2010). Hereditary Tumours: guidelines for diagnostics and prevention. 3rd edition, 2005 and 4th edition Netherlands Foundation for the Detection of Hereditary Tumours (STOET) and Dutch Society for Clinical Genetics (VKGN). (2005, 2010). Hereditary Tumours: guidelines for diagnostics and prevention. 3rd edition, 2005 and 4th edition
go back to reference Pal, T., Permuth-Wey, J., Betts, J. A., Krischer, J. P., Fiorica, J., Arango, H., et al. (2005). BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer, 104(12), 2807–2816.PubMedCrossRef Pal, T., Permuth-Wey, J., Betts, J. A., Krischer, J. P., Fiorica, J., Arango, H., et al. (2005). BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer, 104(12), 2807–2816.PubMedCrossRef
go back to reference Plaschke, J., Engel, C., Krüger, S., Holinski-Feder, E., Pagenstecher, C., Mangold, E., et al. (2004). Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German hereditary nonpolyposis colorectal cancer consortium. Journal of Clinical Oncology, 22(22), 4486–4494.PubMedCrossRef Plaschke, J., Engel, C., Krüger, S., Holinski-Feder, E., Pagenstecher, C., Mangold, E., et al. (2004). Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German hereditary nonpolyposis colorectal cancer consortium. Journal of Clinical Oncology, 22(22), 4486–4494.PubMedCrossRef
go back to reference Pruthi, S., Gostout, B. S., & Lindor, N. M. (2010). Identification and management of women with BRCA mutations or hereditary predisposition for breast and ovarian cancer. Mayo Clinic Proceedings, 85(12), 1111–1120.PubMedCrossRef Pruthi, S., Gostout, B. S., & Lindor, N. M. (2010). Identification and management of women with BRCA mutations or hereditary predisposition for breast and ovarian cancer. Mayo Clinic Proceedings, 85(12), 1111–1120.PubMedCrossRef
go back to reference Ramsoekh, D., Wagner, A., Van Leerdam, M. E., Dinjens, W. N., Steyerberg, E. W., Halley, D. J., et al. (2008). A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting. Gut, 57(11), 1539–1544.PubMedCrossRef Ramsoekh, D., Wagner, A., Van Leerdam, M. E., Dinjens, W. N., Steyerberg, E. W., Halley, D. J., et al. (2008). A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting. Gut, 57(11), 1539–1544.PubMedCrossRef
go back to reference Ready, K. J., Daniels, M. S., Sun, C. C., Peterson, S. K., Northrup, H., & Lu, K. H. (2010). Obstetrics/gynecology residents’ knowledge of hereditary breast and ovarian cancer and Lynch syndrome. Journal of Cancer Education, 25(3), 401–404.PubMedCrossRef Ready, K. J., Daniels, M. S., Sun, C. C., Peterson, S. K., Northrup, H., & Lu, K. H. (2010). Obstetrics/gynecology residents’ knowledge of hereditary breast and ovarian cancer and Lynch syndrome. Journal of Cancer Education, 25(3), 401–404.PubMedCrossRef
go back to reference Renkonen-Sinisalo, L., Bützow, R., Leminen, A., Lehtovirta, P., Mecklin, J. P., & Järvinen, H. J. (2006). Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome. International Journal of Cancer, 120(4), 821–824.CrossRef Renkonen-Sinisalo, L., Bützow, R., Leminen, A., Lehtovirta, P., Mecklin, J. P., & Järvinen, H. J. (2006). Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome. International Journal of Cancer, 120(4), 821–824.CrossRef
go back to reference Resnick, K., Straughn, J. M., Jr., Backes, F., Hampel, H., Matthews, K. S., & Cohn, D. E. (2009). Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients. Obstetrics and Gynecology, 114(3), 530–536.PubMedCrossRef Resnick, K., Straughn, J. M., Jr., Backes, F., Hampel, H., Matthews, K. S., & Cohn, D. E. (2009). Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients. Obstetrics and Gynecology, 114(3), 530–536.PubMedCrossRef
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.PubMedCrossRef 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.PubMedCrossRef
go back to reference Rubin, S. C., Blackwood, M. A., Bandera, C., Behbakht, K., Benjamin, I., et al. (1998). BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing. American Journal of Obstetrics and Gynecology, 178(4), 670–677.PubMedCrossRef Rubin, S. C., Blackwood, M. A., Bandera, C., Behbakht, K., Benjamin, I., et al. (1998). BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing. American Journal of Obstetrics and Gynecology, 178(4), 670–677.PubMedCrossRef
go back to reference Sarantaus, L., Vahteristo, P., Bloom, E., Tamminen, A., Unkila-Kallio, L., et al. (2001). BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients. European Journal of Human Genetics, 9(6), 424–430.PubMedCrossRef Sarantaus, L., Vahteristo, P., Bloom, E., Tamminen, A., Unkila-Kallio, L., et al. (2001). BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients. European Journal of Human Genetics, 9(6), 424–430.PubMedCrossRef
go back to reference Schlich-Bakker, K. J., Ten Kroode, H. F., Wárlám-Rodenhuis, C. C., Van den Bout, J., & Ausems, M. G. (2007). Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer. Genetics in Medicine, 9(11), 766–777.PubMedCrossRef Schlich-Bakker, K. J., Ten Kroode, H. F., Wárlám-Rodenhuis, C. C., Van den Bout, J., & Ausems, M. G. (2007). Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer. Genetics in Medicine, 9(11), 766–777.PubMedCrossRef
go back to reference Sijmons, R. H., Boonstra, A. E., Reefhuis, J., Hordijk-Hos, J. M., De Walle, H. E., et al. (2000). Accuracy of family history of cancer: clinical genetic implications. European Journal of Human Genetics, 8(3), 181–186.PubMedCrossRef Sijmons, R. H., Boonstra, A. E., Reefhuis, J., Hordijk-Hos, J. M., De Walle, H. E., et al. (2000). Accuracy of family history of cancer: clinical genetic implications. European Journal of Human Genetics, 8(3), 181–186.PubMedCrossRef
go back to reference Soegaard, M., Kjaer, S. K., Cox, M., Wozniak, E., Høgdall, E., Høgdall, C., et al. (2008). BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark. Clinical Cancer Research, 14(12), 3761–3767.PubMedCrossRef Soegaard, M., Kjaer, S. K., Cox, M., Wozniak, E., Høgdall, E., Høgdall, C., et al. (2008). BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark. Clinical Cancer Research, 14(12), 3761–3767.PubMedCrossRef
go back to reference Tonin, P. N., Mes-Masson, A. M., Narod, S. A., Ghadirian, P., & Provencher, D. (1999). Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history. Clinical Genetics, 55(5), 318–324.PubMedCrossRef Tonin, P. N., Mes-Masson, A. M., Narod, S. A., Ghadirian, P., & Provencher, D. (1999). Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history. Clinical Genetics, 55(5), 318–324.PubMedCrossRef
go back to reference Tonin, P. N., Maugard, C. M., Perret, C., Mes-Masson, A. M., & Provencher, D. M. (2007). A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families. Familial Cancer, 6(4), 491–497.PubMedCrossRef Tonin, P. N., Maugard, C. M., Perret, C., Mes-Masson, A. M., & Provencher, D. M. (2007). A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families. Familial Cancer, 6(4), 491–497.PubMedCrossRef
go back to reference Trainer, A. H., Meiser, B., Watts, K., Mitchell, G., Tucker, K., & Friedlander, M. (2010). Moving toward personalized medicine: treatment-focused genetic testing of women newly diagnosed with ovarian cancer. International Journal of Gynecological Cancer, 20(5), 704–716.PubMedCrossRef Trainer, A. H., Meiser, B., Watts, K., Mitchell, G., Tucker, K., & Friedlander, M. (2010). Moving toward personalized medicine: treatment-focused genetic testing of women newly diagnosed with ovarian cancer. International Journal of Gynecological Cancer, 20(5), 704–716.PubMedCrossRef
go back to reference Umar, A., Boland, C. R., Terdiman, J. P., Syngal, S., De la Chapelle, A., Rüschoff, J., et al. (2004). Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. Journal of the National Cancer Institute, 96(4), 261–268.PubMedCrossRef Umar, A., Boland, C. R., Terdiman, J. P., Syngal, S., De la Chapelle, A., Rüschoff, J., et al. (2004). Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. Journal of the National Cancer Institute, 96(4), 261–268.PubMedCrossRef
go back to reference Van Asperen, C. J., Van Dijk, S., Zoeteweij, M. W., Timmermans, D. R., De Bock, G. H., Meijers-Heijboer, E. J., et al. (2002). What do women really want to know? Motives for attending familial breast cancer clinics. Journal of Medical Genetics, 39(6), 410–414.PubMedCrossRef Van Asperen, C. J., Van Dijk, S., Zoeteweij, M. W., Timmermans, D. R., De Bock, G. H., Meijers-Heijboer, E. J., et al. (2002). What do women really want to know? Motives for attending familial breast cancer clinics. Journal of Medical Genetics, 39(6), 410–414.PubMedCrossRef
go back to reference Van der Kolk, D. M., de Bock, G. H., Leegte, B. K., Schaapveld, M., Mourits, M. J., de Vries, J., et al. (2010). Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age. Breast Cancer Research and Treatment, 124(3), 643–651.PubMedCrossRef Van der Kolk, D. M., de Bock, G. H., Leegte, B. K., Schaapveld, M., Mourits, M. J., de Vries, J., et al. (2010). Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age. Breast Cancer Research and Treatment, 124(3), 643–651.PubMedCrossRef
go back to reference Van Riel, E., Wárlám-Rodenhuis, C. C., Verhoef, S., Rutgers, E. J., & Ausems, M. G. (2010). BRCA testing of breast cancer patients: medical specialists’ referral patterns, knowledge and attitudes to genetic testing. European Journal of Cancer Care, 19(3), 369–376.PubMedCrossRef Van Riel, E., Wárlám-Rodenhuis, C. C., Verhoef, S., Rutgers, E. J., & Ausems, M. G. (2010). BRCA testing of breast cancer patients: medical specialists’ referral patterns, knowledge and attitudes to genetic testing. European Journal of Cancer Care, 19(3), 369–376.PubMedCrossRef
go back to reference Vasen, H. F. (2005). Clinical description of the Lynch syndrome [hereditary nonpolyposis colorectal cancer (HNPCC)]. Familial Cancer, 4(3), 219–225.PubMedCrossRef Vasen, H. F. (2005). Clinical description of the Lynch syndrome [hereditary nonpolyposis colorectal cancer (HNPCC)]. Familial Cancer, 4(3), 219–225.PubMedCrossRef
go back to reference Vasen, H. F., Watson, P., Mecklin, J. P., & Lynch, H. T. (1999). New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch Syndrome) proposed by the international collaborative group on HNPCC. Gastroenterology, 116(6), 1453–1456.PubMedCrossRef Vasen, H. F., Watson, P., Mecklin, J. P., & Lynch, H. T. (1999). New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch Syndrome) proposed by the international collaborative group on HNPCC. Gastroenterology, 116(6), 1453–1456.PubMedCrossRef
go back to reference Weissman, S. M., Burt, R., Church, J., Erdman, S., Hampel, H., Holter, S., et al. (2012). Identification of individuals at risk for lynch syndrome using targeted evaluations and genetic testing: national society of genetic counselors and the collaborative group of the Americas on inherited colorectal cancer joint practice guideline. Journal of Genetic Counseling, 21(4), 484–493.PubMedCrossRef Weissman, S. M., Burt, R., Church, J., Erdman, S., Hampel, H., Holter, S., et al. (2012). Identification of individuals at risk for lynch syndrome using targeted evaluations and genetic testing: national society of genetic counselors and the collaborative group of the Americas on inherited colorectal cancer joint practice guideline. Journal of Genetic Counseling, 21(4), 484–493.PubMedCrossRef
go back to reference Wevers, M. R., Hahn, D. E., Verhoef, S., Bolhaar, M. D., Ausems, M. G., Aaronson, N. K., et al. (2012). Breast cancer genetic counseling after diagnosis but before treatment: A pilot study on treatment consequences and psychological impact. Patient Education and Counseling; in press Wevers, M. R., Hahn, D. E., Verhoef, S., Bolhaar, M. D., Ausems, M. G., Aaronson, N. K., et al. (2012). Breast cancer genetic counseling after diagnosis but before treatment: A pilot study on treatment consequences and psychological impact. Patient Education and Counseling; in press
go back to reference Wideroff, L., Vadaparampil, S. T., Greene, M. H., Taplin, S., Olson, L., & Freedman, A. N. (2005). Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians. Journal of Medical Genetics, 42(10), 749–755.PubMedCrossRef Wideroff, L., Vadaparampil, S. T., Greene, M. H., Taplin, S., Olson, L., & Freedman, A. N. (2005). Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians. Journal of Medical Genetics, 42(10), 749–755.PubMedCrossRef
go back to reference Wijnen, J., De Leeuw, W., Vasen, H., Van der Klift, H., Møller, P., Stormorken, A., et al. (1999). Familial endometrial cancer in female carriers of MSH6 germline mutations. Nature Genetics, 23(2), 142–144.PubMedCrossRef Wijnen, J., De Leeuw, W., Vasen, H., Van der Klift, H., Møller, P., Stormorken, A., et al. (1999). Familial endometrial cancer in female carriers of MSH6 germline mutations. Nature Genetics, 23(2), 142–144.PubMedCrossRef
go back to reference Yazici, H., Glendon, G., Yazici, H., Burnie, S. J., Saip, P., Buyru, F., et al. (2002). BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: a high incidence of mutations in non-familial cases. Human Mutation, 20(1), 28–34.PubMedCrossRef Yazici, H., Glendon, G., Yazici, H., Burnie, S. J., Saip, P., Buyru, F., et al. (2002). BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: a high incidence of mutations in non-familial cases. Human Mutation, 20(1), 28–34.PubMedCrossRef
go back to reference Yong, M. C., Zhou, X. J., & Lee, S. C. (2003). The importance of paternal family history in hereditary breast cancer is underappreciated by health care professionals. Oncology, 64(3), 220–226.PubMedCrossRef Yong, M. C., Zhou, X. J., & Lee, S. C. (2003). The importance of paternal family history in hereditary breast cancer is underappreciated by health care professionals. Oncology, 64(3), 220–226.PubMedCrossRef
go back to reference Zilliacus, E., Meiser, B., Gleeson, M., Watts, K., Tucker, K., Lobb, E. A., et al. (2012) Are we being overly cautious? A qualitative inquiry into the experiences and perceptions of treatment-focused germline BRCA genetic testing amongst women recently diagnosed with breast cancer. Supportive Care in Cancer; in press. Zilliacus, E., Meiser, B., Gleeson, M., Watts, K., Tucker, K., Lobb, E. A., et al. (2012) Are we being overly cautious? A qualitative inquiry into the experiences and perceptions of treatment-focused germline BRCA genetic testing amongst women recently diagnosed with breast cancer. Supportive Care in Cancer; in press.
Metadata
Title
Acceptance of Genetic Counseling and Testing in a Hospital-Based Series of Patients with Gynecological Cancer
Authors
Nicky Dekker
Eleonora B. L. van Dorst
Rob B. van der Luijt
Marielle E. van Gijn
Marc van Tuil
Johan A. Offerhaus
Margreet G. E. M. Ausems
Publication date
01-06-2013
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 3/2013
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-012-9553-3

Other articles of this Issue 3/2013

Journal of Genetic Counseling 3/2013 Go to the issue