J Breast Cancer.  2008 Jun;11(2):95-101. 10.4048/jbc.2008.11.2.95.

Practice Patterns of Surgeons for the Management of Hereditary Breast Cancer in Korea

Affiliations
  • 1Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam; 1Department of Surgery, Soonchunhyang University College of Medicine, Seoul; 2Department of Surgery, Ulsan University College of Me

Abstract

PURPOSE: The aim of this study is to examine practice patterns of surgeons for the management of hereditary breast cancer in Korea.
METHODS
A structured questionnaire was circulated to the members of the Korean Breast Cancer Society through email distribution between 6 July and 14 August 2007. A total of 43 surgeons from 42 hospitals responded to the survey.
RESULTS
Of the respondents, 81.4% (n=35) asked for information related to the family histories of cancer and 58.1% (n=25) recommended genetic testing for their patients. Indications for genetic testing recommended by the 25 surgeons were the following: breast cancer patients with family histories of breast or ovarian cancer (96%), bilateral breast cancer (80%), early-onset (64%) or male breast cancer (52%), and a double primary malignancy with breast and ovarian cancer (36%). Of the respondents, 52% (13/25) performed genetic counseling before genetic testing, and the surgeons (81.3%, 13/16) or genetic counselors (18.7%, 3/16) provided the genetic counseling. Although 154 BRCA1/2 mutation carriers of 95 families have been identified so far, only 12 family members were managed for prophylaxis by tamoxifen chemoprevention (n=2), a contralateral prophylactic mastectomy (n=2) or a prophylactic oophorectomy (n=8). There was no report of a bilateral prophylactic mastectomy being performed.
CONCLUSION
Although BRCA1/2 mutation carriers for highrisk patients with hereditary breast cancer have been identified in Korea, practice and management for cancer prevention does not seem to be actively performed. The Korean Hereditary Breast Cancer (KOHBRA) Study will serve to establish the Korean guidelines of evidence-based clinical practice for hereditary breast cancer.

Keyword

Hereditary breast cancer; Practice patterns for management; Questionnaire

MeSH Terms

Breast
Breast Neoplasms
Breast Neoplasms, Male
Chemoprevention
Counseling
Surveys and Questionnaires
Electronic Mail
Female
Genetic Counseling
Genetic Testing
Humans
Korea
Male
Mastectomy
Ovarian Neoplasms
Ovariectomy
Tamoxifen
Tamoxifen

Cited by  10 articles

Contralateral Prophylactic Mastectomy and Prophylactic Salphingo-Oophorectomy in a BRCA1-Positive Breast Cancer Patient: A Case Report
Ku Sang Kim, Sairhee Kim, Sang Ah Han, Eunyoung Kang, Yong Tark Jeon, Tae-Hyeon Ha, Chan-Yeong Heo, Mijung Jang, Sun Mi Kim, Jee Hyun Kim, Kyu Eun Lee, Sung-Won Kim
J Breast Cancer. 2008;11(4):218-222.    doi: 10.4048/jbc.2008.11.4.218.

The Breast and Ovarian Cancer Risks in Korea Due to Inherited Mutations in BRCA1 and BRCA2: A Preliminary Report
Sang Ah Han, Sue K. Park, Sei-Hyun Ahn, Byung Ho Son, Min Hyuk Lee, Doo Ho Choi, Dong-Young Noh, Wonshik Han, Eun Sook Lee, Seo Kyung Han, Lee Su Kim, Yongsik Jung, Ku Sang Kim, Young Jin Suh, Byung-In Moon, Seok-Jin Nam, Woo-Chul Noh, Jeong Eon Lee, Sung-Won Kim,
J Breast Cancer. 2009;12(2):92-99.    doi: 10.4048/jbc.2009.12.2.92.

Incidental Detection of Ductal Carcinoma In Situ of the Breast from Bilateral Prophylactic Mastectomy of Asymptomatic BRCA2 Mutation Carrier: A Case Report
Min-Young Choi, Jeong Eon Lee, Sung-Won Kim, Se Kyung Lee, Sung Mo Hur, Sangmin Kim, Min Young Koo, Soo Youn Bae, Jun-Ho Choe, Jung-Han Kim, Jee Soo Kim, Seok Jin Nam, Jung-Hyun Yang
J Breast Cancer. 2010;13(3):311-317.    doi: 10.4048/jbc.2010.13.3.311.

Single-Port Access Laparoscopic Prophylactic Bilateral Salpingo-Oophorectomy in BRCA-Positive Breast Cancer Patient: A Case Report
Tae-Joong Kim, Min-Young Choi, Se Kyung Lee, Sung Mo Hur, Sangmin Kim, Min Young Koo, Soo Youn Bae, Dong Hui Cho, Jun-Ho Choe, Jung-Han Kim, Jee Soo Kim, Byoung-Gie Kim, Duk-Soo Bae, Jeong Eon Lee, Seok Jin Nam, Jung-Hyun Yang
J Breast Cancer. 2010;13(4):437-442.    doi: 10.4048/jbc.2010.13.4.437.

The Change of Practice Patterns of the Hereditary Breast Cancer Management in Korea after the Korean Hereditary Breast Cancer Study
Eunyoung Kang, Sei-Hyun Ahn, Woo-Chul Noh, Dong-Young Noh, Yongsik Jung, Lee Su Kim, Doo Ho Choi, Young Jin Suh, Ku Sang Kim, Jeong Eon Lee, Min Hyuk Lee, Seok-Jin Nam, Byung-In Moon, Byung Ho Son, Jung-Hyun Yang, Cha Kyong Yom, Sung Yong Kim, Sue K. Park, Sung-Won Kim,
J Breast Cancer. 2010;13(4):418-430.    doi: 10.4048/jbc.2010.13.4.418.

Usage Patterns of Surveillance, Chemoprevention and Risk-Reducing Surgery in Korean BRCA Mutation Carriers: 5 Years of Experience at a Single Institution
Do Hoon Koo, Il Yong Chung, Eunyoung Kang, Sang Ah Han, Sung-Won Kim
J Breast Cancer. 2011;14(Suppl 1):S17-S23.    doi: 10.4048/jbc.2011.14.S.S17.

The Prevalence of Ovarian Cancer in Korean Women at High-Risk for Hereditary Breast-Ovarian Cancer
Jihyoun Lee, Eunyoung Kang, Sung-Won Kim, Boyoung Park, Sue K. Park, Sei-Hyun Ahn, Hy-De Lee, Joon Jeong, Sung Hoo Jung, Byoung Kil Lee, Myung Chul Chang, Young Tae Bae, Young Up Cho, Ki-Tae Hwang, Hyun-Ah Kim, Eun-Kyu Kim, Nam Sun Paik, Sehwan Han, Chan Seok Yoon, Min Hyuk Lee,
J Breast Cancer. 2011;14(Suppl 1):S24-S30.    doi: 10.4048/jbc.2011.14.S.S24.

The Korean Hereditary Breast Cancer Study: Review and Future Perspectives
Eunyoung Kang, Sung-Won Kim
J Breast Cancer. 2013;16(3):245-253.    doi: 10.4048/jbc.2013.16.3.245.

Korean Hereditary Breast Cancer
Sung-Won Kim
J Korean Med Assoc. 2009;52(10):952-962.    doi: 10.5124/jkma.2009.52.10.952.

The Effect of the Cancer Genetic Education Program for Nurses
Kyung Sook Choi, Eun Sil Jang, Myung-Hee Jun, Ji-Young Jung, Jung Ae Park
J Korean Oncol Nurs. 2010;10(2):240-246.    doi: 10.5388/jkon.2010.10.2.240.


Reference

1. Claus EB, Schildkraut JM, Thompson WD, Risch NJ. The genetic attributable risk of breast and ovarian cancer. Cancer. 1996. 77:2318–2324.
Article
2. Friedman LS, Ostermeyer EA, Szabo CI, Dowd P, Lynch ED, Rowell SE, et al. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat Genet. 1994. 8:399–404.
Article
3. Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, et al. Identification of the breast cancer susceptibility gene BRCA2. Nature. 1995. 378:789–792.
Article
4. Kang DH, Kim SW, Noh DY, Ahn YO, You KY. Hereditary breast cancer syndrome. Breast. 2005. 2:179–188.
5. Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, et al. 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. Am J Hum Genet. 2003. 72:1117–1130.
Article
6. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families: the breast cancer linkage consortium. Am J Hum Genet. 1998. 62:676–689.
Article
7. Kim SW, Lee CS, Fey JV, Borgen PI, Boyd J. Prevalence of BRCA2 mutations in a hospital based series of unselected breast cancer cases. J Med Genet. 2005. 42:e5.
Article
8. Couch FJ, DeShano ML, Blackwood MA, Calzone K, Stopfer J, Campeau L, et al. BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. N Engl J Med. 1997. 336:1409–1415.
Article
9. Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, et al. BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing. JAMA. 1997. 278:1242–1250.
Article
10. Frank TS, Deffenbaugh AM, Reid JE, Hulick M, Ward BE, Lingenfelter B, et al. Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. J Clin Oncol. 2002. 20:1480–1490.
Article
11. Ferla CV, Cascio S, Rinaldi G, Badalamenti G, Carreca I, Surmacz E, et al. Founder mutations in BRCA1 and BRCA2 genes. Ann Oncol. 2007. 18:93–98.
Article
12. Warner E, Foulkes W, Goodwin P, Meschino W, Blondal J, Paterson C, et al. Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer. J Natl Cancer Inst. 1999. 91:1241–1247.
Article
13. Johannesdottir G, Gudmundsson J, Bergthorsson JT, Arason A, Agnarsson BA, Eiriksdottir G, et al. High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients. Cancer Res. 1996. 56:3663–3665.
14. Oh JW, Noh DY, Choi KJ, Kang SB, Kim IS, Noh MS, et al. BRCA 1 germline mutation in Korean breast and ovarian cancer patients. J Korean Oncology. 1995. 27:1061–1069.
15. Kang HC, Kim IJ, Park JH, Kwon HJ, Won YJ, Heo SC, et al. Germline mutations of BRCA1 and BRCA2 in Korean breast and/or ovarian cancer families. Hum Mutat. 2002. 20:235.
Article
16. Choi DH, Lee MH, Bale AE, Carter D, Haffty BG. Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. J Clin Oncol. 2004. 22:1638–1645.
Article
17. Ahn SH, Son BH, Yoon KS, Noh DY, Han W, Kim SW, et al. BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations. Cancer Letters. 2007. 245:90–95.
Article
18. Green MJ, Biesecker BB, McInerney AM, Mauger D, Fost N. An Interactive Computer Program Can Effectively Educate Patients About Genetic Testing for Breast Cancer Susceptibility. Am J Med Genet. 2001. 103:16–23.
Article
19. Narod SA, Offit K. Prevention and management of hereditary breast cancer. J Clin Oncol. 2005. 23:1656–1663.
Article
20. Meijers-Heijboer H, van Geel B, van Putten WL, Henzen-Logmans SC, Seynaeve C, Menke-Pluymers MB, et al. Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation. N Engl J Med. 2001. 345:159–164.
Article
Full Text Links
  • JBC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr