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Published in: Breast Cancer Research 4/2000

01-08-2000 | Review

Future possibilities in the prevention of breast cancer: Intervention strategies in BRCA1 and BRCA2 mutation carriers

Author: Rosalind A Eeles

Published in: Breast Cancer Research | Issue 4/2000

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Abstract

The development of intervention strategies for carriers of mutations in the BRCA1 and BRCA2 genes has several considerations. The first are primary prevention and secondary prevention in unaffected carriers using medical/surgical or lifestyle strategies to prevent cancer development, or screening methods to detect cancers at an earlier stage. The options available are determined by the magnitude and age at onset, risk profile of cancer in carriers (the penetrance function of the gene) and the different cancer sites involved. The management of affected individuals who are BRCA1 and BRCA2 mutation carriers may be altered by their carrier status, because the tumour histology, efficacy of treatment and risk of subsequent cancer development is determined by the BRCA1 and BRCA2 germline status. Carriers of BRCA1 and BRCA2 mutations are relatively rare, so the strategies for management should be determined by international multicentre studies.
Literature
1.
go back to reference Easton D, Peto J: The contribution of inherited predisposition to cancer incidence. Cancer Surveys. 1990, 9: 395-416.PubMed Easton D, Peto J: The contribution of inherited predisposition to cancer incidence. Cancer Surveys. 1990, 9: 395-416.PubMed
2.
go back to reference Claus EB, Risch N, Thompson WD: Genetic analysis of breast cancer in the Cancer and Steroid Hormone study. Am J Hum Genet. 1991, 48: 232-242.PubMedPubMedCentral Claus EB, Risch N, Thompson WD: Genetic analysis of breast cancer in the Cancer and Steroid Hormone study. Am J Hum Genet. 1991, 48: 232-242.PubMedPubMedCentral
3.
go back to reference Easton DF, Ford D, Bishop DT, and the Breast Cancer Linkage Consortium : Breast and ovarian cancer incidence in BRCA 1 carriers. Am J Hum Genet. 1995, 56: 265-271.CrossRefPubMedPubMedCentral Easton DF, Ford D, Bishop DT, and the Breast Cancer Linkage Consortium : Breast and ovarian cancer incidence in BRCA 1 carriers. Am J Hum Genet. 1995, 56: 265-271.CrossRefPubMedPubMedCentral
4.
go back to reference Miki Y, Swensen J, Shattuck-Eidens D, et al: A strong candidate for the breast and ovarian cancer susceptibility gene, BRCA 1. Science. 1994, 266: 66-71., This paper describes the cloning of the BRCA1 geneCrossRefPubMed Miki Y, Swensen J, Shattuck-Eidens D, et al: A strong candidate for the breast and ovarian cancer susceptibility gene, BRCA 1. Science. 1994, 266: 66-71., This paper describes the cloning of the BRCA1 geneCrossRefPubMed
5.
go back to reference Wooster R, Bignell G, Lancaster J, et al: Identification of a breast cancer gene, BRCA2. Nature . 1995, 378: 789-791. 10.1038/378789a0., This paper describes the cloning of the BRCA2 geneCrossRefPubMed Wooster R, Bignell G, Lancaster J, et al: Identification of a breast cancer gene, BRCA2. Nature . 1995, 378: 789-791. 10.1038/378789a0., This paper describes the cloning of the BRCA2 geneCrossRefPubMed
6.
go back to reference Ford D, Easton DF, Peto J: Estimates of the gene frequency of BRCA-1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet. 1995, 57: 1457-1462.PubMedPubMedCentral Ford D, Easton DF, Peto J: Estimates of the gene frequency of BRCA-1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet. 1995, 57: 1457-1462.PubMedPubMedCentral
7.
go back to reference Ford D, Easton DF, Stratton MR, et al: Genetic heterogeneity and penetrance analysis of the BRCA 1 and BRCA2 genes in breast cancer families. Am J Hum Genet. 1998, 62: 676-689. 10.1086/301749., This paper describes the proportion of high-risk families due to BRCA1 and BRCA2 and their phenotypic characteristics and is used by cancer geneticists when quoting penetrance figures for the high-risk familiesCrossRefPubMedPubMedCentral Ford D, Easton DF, Stratton MR, et al: Genetic heterogeneity and penetrance analysis of the BRCA 1 and BRCA2 genes in breast cancer families. Am J Hum Genet. 1998, 62: 676-689. 10.1086/301749., This paper describes the proportion of high-risk families due to BRCA1 and BRCA2 and their phenotypic characteristics and is used by cancer geneticists when quoting penetrance figures for the high-risk familiesCrossRefPubMedPubMedCentral
8.
go back to reference Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE: Risks of cancer in BRCA 1-mutation carriers. Lancet. 1994, 343: 692-695. 10.1016/S0140-6736(94)91578-4., This is the seminal paper outlining the risks of other cancers, apart from breast cancer in BRCA1 carriersCrossRefPubMed Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE: Risks of cancer in BRCA 1-mutation carriers. Lancet. 1994, 343: 692-695. 10.1016/S0140-6736(94)91578-4., This is the seminal paper outlining the risks of other cancers, apart from breast cancer in BRCA1 carriersCrossRefPubMed
9.
go back to reference Phelan CM, Lancaster JM, Tonin P, et al: Mutation analysis of the BRCA 2 gene in 49 site-specific breast cancer families. Nature Genet. 1996, 13: 120-122.CrossRefPubMed Phelan CM, Lancaster JM, Tonin P, et al: Mutation analysis of the BRCA 2 gene in 49 site-specific breast cancer families. Nature Genet. 1996, 13: 120-122.CrossRefPubMed
10.
go back to reference Breast Cancer Linkage Consortium: Carrier risks in BRCA 2 mutation carriers. J Natl Cancer Inst. 1999, 91: 1310-1316. 10.1093/jnci/91.15.1310., This is the seminal paper outlining the risks of other cancers, apart from breast cancer in BRCA2 carriersCrossRef Breast Cancer Linkage Consortium: Carrier risks in BRCA 2 mutation carriers. J Natl Cancer Inst. 1999, 91: 1310-1316. 10.1093/jnci/91.15.1310., This is the seminal paper outlining the risks of other cancers, apart from breast cancer in BRCA2 carriersCrossRef
11.
go back to reference Struewing JP, Hartge P, Wacholder S, et al: The risk of cancer associated with specific mutations of BRCA 1 and BRCA2 among Ashkenazi Jews. N Engl J Med. 1997, 336: 1401-1408. 10.1056/NEJM199705153362001.CrossRefPubMed Struewing JP, Hartge P, Wacholder S, et al: The risk of cancer associated with specific mutations of BRCA 1 and BRCA2 among Ashkenazi Jews. N Engl J Med. 1997, 336: 1401-1408. 10.1056/NEJM199705153362001.CrossRefPubMed
12.
go back to reference Thorlacius S, Struewing JP, Hartge P, et al: Population-based study of risk of breast cancer in carriers of BRCA 2 mutation. Lancet. 1998, 352: 1337-1339. 10.1016/S0140-6736(98)03300-5.CrossRefPubMed Thorlacius S, Struewing JP, Hartge P, et al: Population-based study of risk of breast cancer in carriers of BRCA 2 mutation. Lancet. 1998, 352: 1337-1339. 10.1016/S0140-6736(98)03300-5.CrossRefPubMed
13.
go back to reference Gayther SA, Warren W, Mazoyer S, et al: Germline mutations of the BRCA 1 gene in breast/ovarian cancer families: evidence for a genotype/phenotype correlation. Nature Genet. 1995, 11: 428-433.CrossRefPubMed Gayther SA, Warren W, Mazoyer S, et al: Germline mutations of the BRCA 1 gene in breast/ovarian cancer families: evidence for a genotype/phenotype correlation. Nature Genet. 1995, 11: 428-433.CrossRefPubMed
14.
go back to reference Eeles R, Kaduri L: BRCA 1/2 carriers and endocrine risk modifiers. Endocrine-Related Cancer. 1999, 6: 521-528.CrossRefPubMed Eeles R, Kaduri L: BRCA 1/2 carriers and endocrine risk modifiers. Endocrine-Related Cancer. 1999, 6: 521-528.CrossRefPubMed
15.
go back to reference Shattuck-Eidens D, McClure M, Simard J, et al: A collaborative survey of 80 mutations in the BRCA 1 breast and ovarian cancer susceptibility gene. JAMA. 1995, 273: 535-541. 10.1001/jama.273.7.535.CrossRefPubMed Shattuck-Eidens D, McClure M, Simard J, et al: A collaborative survey of 80 mutations in the BRCA 1 breast and ovarian cancer susceptibility gene. JAMA. 1995, 273: 535-541. 10.1001/jama.273.7.535.CrossRefPubMed
16.
go back to reference Shattuck-Eidens D, Oliphant A, McClure M, et al: BRCA 1 sequence analysis in women at high risk for susceptibility mutations. JAMA. 1997, 278: 1242-1250. 10.1001/jama.278.15.1242.CrossRefPubMed Shattuck-Eidens D, Oliphant A, McClure M, et al: BRCA 1 sequence analysis in women at high risk for susceptibility mutations. JAMA. 1997, 278: 1242-1250. 10.1001/jama.278.15.1242.CrossRefPubMed
18.
go back to reference Struewing JP, Abeliovich D, Peretz T, et al: The carrier frequency of the BRCA 1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genet. 1995, 11: 198-200.CrossRefPubMed Struewing JP, Abeliovich D, Peretz T, et al: The carrier frequency of the BRCA 1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genet. 1995, 11: 198-200.CrossRefPubMed
19.
go back to reference Neuhausen S, Gilewski T, Norton L, et al: Recurrent BRCA 2 617delT mutations in Ashkenazi Jewish women affected by breast cancer. Nature Genet. 1996, 13: 126-128.CrossRefPubMed Neuhausen S, Gilewski T, Norton L, et al: Recurrent BRCA 2 617delT mutations in Ashkenazi Jewish women affected by breast cancer. Nature Genet. 1996, 13: 126-128.CrossRefPubMed
20.
go back to reference Oddoux C, Struewing JP, Clayton CM, et al: The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nature Genet . 1996, 14: 188-190.CrossRefPubMed Oddoux C, Struewing JP, Clayton CM, et al: The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nature Genet . 1996, 14: 188-190.CrossRefPubMed
21.
go back to reference Offit K, Gilewski T, McGuire P, et al: Germline BRCA 1 185delAG mutations in Jewish women with breast cancer. Lancet. 1996, 347: 1643-1645. 10.1016/S0140-6736(96)91484-1.CrossRefPubMed Offit K, Gilewski T, McGuire P, et al: Germline BRCA 1 185delAG mutations in Jewish women with breast cancer. Lancet. 1996, 347: 1643-1645. 10.1016/S0140-6736(96)91484-1.CrossRefPubMed
22.
go back to reference Roa BB, Boyd AA, Volcik K, Richards CS: Ashkenazi Jewish population frequencies for common mutations in BRCA 1 and BRCA 2. Nature Genet. 1996, 14: 185-187., This paper gives results for the frequency of BRCA1 and BRCA2 mutations in Ashkenazi familiesCrossRefPubMed Roa BB, Boyd AA, Volcik K, Richards CS: Ashkenazi Jewish population frequencies for common mutations in BRCA 1 and BRCA 2. Nature Genet. 1996, 14: 185-187., This paper gives results for the frequency of BRCA1 and BRCA2 mutations in Ashkenazi familiesCrossRefPubMed
23.
go back to reference Tonin P, Weber B, Offit K, et al: A high frequency of BRCA 1 and BRCA 2 mutations in 222 Ashkenazi Jewish breast cancer families. Nature Med. 1996, 2: 1179-1183.CrossRefPubMed Tonin P, Weber B, Offit K, et al: A high frequency of BRCA 1 and BRCA 2 mutations in 222 Ashkenazi Jewish breast cancer families. Nature Med. 1996, 2: 1179-1183.CrossRefPubMed
24.
go back to reference Craufurd D, Tyler A: Predictive testing for Huntington's disease: protocol of the UK Huntington's Prediction Consortium. J Med Genet. 1992, 29: 915-918.CrossRefPubMedPubMedCentral Craufurd D, Tyler A: Predictive testing for Huntington's disease: protocol of the UK Huntington's Prediction Consortium. J Med Genet. 1992, 29: 915-918.CrossRefPubMedPubMedCentral
25.
go back to reference Langston AA, Malone KE, Thompson JD, Daling JR, Ostrander EA: BRCA1 mutations in a population-based sample of young women with breast cancer. N Engl J Med. 1996, 334: 137-142. 10.1056/NEJM199601183340301.CrossRefPubMed Langston AA, Malone KE, Thompson JD, Daling JR, Ostrander EA: BRCA1 mutations in a population-based sample of young women with breast cancer. N Engl J Med. 1996, 334: 137-142. 10.1056/NEJM199601183340301.CrossRefPubMed
26.
go back to reference Chamberlain J: Screening for breast cancer in high-risk populations. In: Genetic Predisposition to Cancer. Edited by Eeles R, Ponder B, Easton D, Horwich A. UK: Chapman and Hall;. 1996 Chamberlain J: Screening for breast cancer in high-risk populations. In: Genetic Predisposition to Cancer. Edited by Eeles R, Ponder B, Easton D, Horwich A. UK: Chapman and Hall;. 1996
27.
go back to reference Eccles DM, Evans DGR, Mackay J, et al: Guidelines for a genetic risk-based approach to advising women with a family history of breast cancer. J Med Genet. 2000, 37: 203-209. 10.1136/jmg.37.3.203.CrossRefPubMedPubMedCentral Eccles DM, Evans DGR, Mackay J, et al: Guidelines for a genetic risk-based approach to advising women with a family history of breast cancer. J Med Genet. 2000, 37: 203-209. 10.1136/jmg.37.3.203.CrossRefPubMedPubMedCentral
28.
go back to reference Lalloo F, Boggis CR, Evans DG, Shenton A, Threlfall AG, Howell A: Screening by mammography, women with a family history of breast cancer. Eur J Cancer. 1998, 34: 937-940. 10.1016/S0959-8049(98)00005-7.CrossRefPubMed Lalloo F, Boggis CR, Evans DG, Shenton A, Threlfall AG, Howell A: Screening by mammography, women with a family history of breast cancer. Eur J Cancer. 1998, 34: 937-940. 10.1016/S0959-8049(98)00005-7.CrossRefPubMed
29.
go back to reference Klemi PJ, Toikkanen S, Rasanen O, Parvinen I, Joensuu H: Mammographic screening interval and the frequency of interval cancers in a population-based screening. Br J Cancer. 1997, 75: 762-766.CrossRefPubMedPubMedCentral Klemi PJ, Toikkanen S, Rasanen O, Parvinen I, Joensuu H: Mammographic screening interval and the frequency of interval cancers in a population-based screening. Br J Cancer. 1997, 75: 762-766.CrossRefPubMedPubMedCentral
30.
go back to reference Tokunaga M, Land CE, Tokuoka S, Nishimori I, Soda M, Akiba S: Incidence of female breast cancer among atomic bomb survivors, 1950-1985. Radiat Res. 1994, 138: 209-223.CrossRefPubMed Tokunaga M, Land CE, Tokuoka S, Nishimori I, Soda M, Akiba S: Incidence of female breast cancer among atomic bomb survivors, 1950-1985. Radiat Res. 1994, 138: 209-223.CrossRefPubMed
31.
go back to reference Kote-Jarai Z, Eeles RA: BRCA1, BRCA2 and their possible function in DNA damage response. Br J Cancer. 1999, 81: 1099-1102. 10.1038/sj.bjc.6690814., This review summarises the evidence that BRCA1 and BRCA2 are involved in the DNA damage responseCrossRefPubMedPubMedCentral Kote-Jarai Z, Eeles RA: BRCA1, BRCA2 and their possible function in DNA damage response. Br J Cancer. 1999, 81: 1099-1102. 10.1038/sj.bjc.6690814., This review summarises the evidence that BRCA1 and BRCA2 are involved in the DNA damage responseCrossRefPubMedPubMedCentral
32.
go back to reference Peacock J, McMillan T, Eeles R, et al: Radio-sensitivity of patients carrying defects in the BRCA1 gene. Lancet . 2000, Peacock J, McMillan T, Eeles R, et al: Radio-sensitivity of patients carrying defects in the BRCA1 gene. Lancet . 2000,
33.
go back to reference Locker AP, Caseldine J, Mitchell AK, Blamey RW, Roebuck EJ, Elston CW: Results from a seven-year programme of breast self-examination in 89,010 women. Br J Cancer. 1989, 60: 401-405.CrossRefPubMedPubMedCentral Locker AP, Caseldine J, Mitchell AK, Blamey RW, Roebuck EJ, Elston CW: Results from a seven-year programme of breast self-examination in 89,010 women. Br J Cancer. 1989, 60: 401-405.CrossRefPubMedPubMedCentral
35.
go back to reference Lakhani S, Sloane JP, Gusterson BA, et al: A detailed analysis of the morphological features associated with breast cancer in patients harbouring mutations in BRCA 1 and BRCA 2 predisposition genes. J Natl Cancer Inst. 1999, 90: 1138-1145. 10.1093/jnci/90.15.1138., This paper showed that the pathological features of breast cancers occurring in BRCA1 carriers are different from those in BRCA2 carriers and those without mutations in either of these genesCrossRef Lakhani S, Sloane JP, Gusterson BA, et al: A detailed analysis of the morphological features associated with breast cancer in patients harbouring mutations in BRCA 1 and BRCA 2 predisposition genes. J Natl Cancer Inst. 1999, 90: 1138-1145. 10.1093/jnci/90.15.1138., This paper showed that the pathological features of breast cancers occurring in BRCA1 carriers are different from those in BRCA2 carriers and those without mutations in either of these genesCrossRef
36.
go back to reference Jacobs IJ, Skates SJ, MacDonald N, et al: Screening for ovarian cancer: a pilot randomised controlled trial. Lancet. 1999, 353: 1207-1210. 10.1016/S0140-6736(98)10261-1.CrossRefPubMed Jacobs IJ, Skates SJ, MacDonald N, et al: Screening for ovarian cancer: a pilot randomised controlled trial. Lancet. 1999, 353: 1207-1210. 10.1016/S0140-6736(98)10261-1.CrossRefPubMed
37.
go back to reference McWhorter WP, Hernandez AO, Meikle AW, et al: A screening study of prostate cancer in high risk families. J Urol . 1992, 148: 826-828.PubMed McWhorter WP, Hernandez AO, Meikle AW, et al: A screening study of prostate cancer in high risk families. J Urol . 1992, 148: 826-828.PubMed
38.
go back to reference Lynch HT, Watson P, Lanspa SJ, et al: Natural history of colorectal cancer in hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II). Dis Colon Rectum. 1988, 31: 439-444.CrossRefPubMed Lynch HT, Watson P, Lanspa SJ, et al: Natural history of colorectal cancer in hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II). Dis Colon Rectum. 1988, 31: 439-444.CrossRefPubMed
39.
go back to reference Brunet JS, Ghadirian P, Rebeck TR, et al: Effect of smoking on breast cancer in carriers of mutant BRCA 1 or BRCA 2 genes. J Natl Cancer Inst. 1998, 90: 761-765. 10.1093/jnci/90.10.761.CrossRefPubMed Brunet JS, Ghadirian P, Rebeck TR, et al: Effect of smoking on breast cancer in carriers of mutant BRCA 1 or BRCA 2 genes. J Natl Cancer Inst. 1998, 90: 761-765. 10.1093/jnci/90.10.761.CrossRefPubMed
40.
go back to reference Struewing JP, Watson P, Easton DF, Ponder BA, Lynch HT, Tucker MA: Prophylactic oophorectomy in inherited breast/ovarian cancer families. J Natl Cancer Inst Monogr. 1995, 17: 33-35., This reference shows that prophylactic oophorectomy reduces ovarian cancer risk Struewing JP, Watson P, Easton DF, Ponder BA, Lynch HT, Tucker MA: Prophylactic oophorectomy in inherited breast/ovarian cancer families. J Natl Cancer Inst Monogr. 1995, 17: 33-35., This reference shows that prophylactic oophorectomy reduces ovarian cancer risk
41.
go back to reference Rebbeck T, Levin AM, Eisen A, et al: Breast cancer risk after bilateral prophylactic oophorectomy in BRCA 1 mutation carriers. J Natl Cancer Inst. 1999, 91: 1475-1479. 10.1093/jnci/91.17.1475., This reference shows that prophylactic oophorectomy reduces both ovarian and breast cancer risk in BRCA carriersCrossRefPubMed Rebbeck T, Levin AM, Eisen A, et al: Breast cancer risk after bilateral prophylactic oophorectomy in BRCA 1 mutation carriers. J Natl Cancer Inst. 1999, 91: 1475-1479. 10.1093/jnci/91.17.1475., This reference shows that prophylactic oophorectomy reduces both ovarian and breast cancer risk in BRCA carriersCrossRefPubMed
42.
go back to reference Jernström H, Lerman C, Ghadirian P, et al: Pregnancy and risk of early breast cancer in carriers of BRCA 1 and BRCA2. Lancet. 1999, 354: 1846-1850. 10.1016/S0140-6736(99)04336-6.CrossRefPubMed Jernström H, Lerman C, Ghadirian P, et al: Pregnancy and risk of early breast cancer in carriers of BRCA 1 and BRCA2. Lancet. 1999, 354: 1846-1850. 10.1016/S0140-6736(99)04336-6.CrossRefPubMed
43.
go back to reference Cuzick J: Future possibilities in the prevention of breast cancer: breast cancer prevention trials. Breast Cancer Res. 2000, Cuzick J: Future possibilities in the prevention of breast cancer: breast cancer prevention trials. Breast Cancer Res. 2000,
44.
go back to reference Fisher B, Costantino JP, Wickerham DL, et al: Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst. 1998, 90: 1371-1388. 10.1093/jnci/90.18.1371., See [46]CrossRefPubMed Fisher B, Costantino JP, Wickerham DL, et al: Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst. 1998, 90: 1371-1388. 10.1093/jnci/90.18.1371., See [46]CrossRefPubMed
45.
go back to reference Powles T, Eeles R, Ashley S, et al: Interim analysis of the incidence of breast cancer in the Royal Marsden Hospital tamoxifen randomised chemoprevention trial. Lancet. 1998, 352: 98-101., See [46]CrossRefPubMed Powles T, Eeles R, Ashley S, et al: Interim analysis of the incidence of breast cancer in the Royal Marsden Hospital tamoxifen randomised chemoprevention trial. Lancet. 1998, 352: 98-101., See [46]CrossRefPubMed
46.
go back to reference Veronesi U, Maisonneuve P, Costa A, et al: Prevention of breast cancer with tamoxifen: preliminary findings from the Italian randomised trial among hysterectomised women. Italian Tamoxifen Prevention Study. Lancet. 1998, 352: 93-97., These three papers [44–46] describe three trials that investigate the role of Tamoxifen as a chemopreventive agent for breast cancerCrossRefPubMed Veronesi U, Maisonneuve P, Costa A, et al: Prevention of breast cancer with tamoxifen: preliminary findings from the Italian randomised trial among hysterectomised women. Italian Tamoxifen Prevention Study. Lancet. 1998, 352: 93-97., These three papers [44–46] describe three trials that investigate the role of Tamoxifen as a chemopreventive agent for breast cancerCrossRefPubMed
47.
go back to reference Lerman C, Narod S, Schulman K, et al: BRCA 1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes. JAMA. 1996, 275: 1885-1892. 10.1001/jama.275.24.1885.CrossRefPubMed Lerman C, Narod S, Schulman K, et al: BRCA 1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes. JAMA. 1996, 275: 1885-1892. 10.1001/jama.275.24.1885.CrossRefPubMed
49.
go back to reference Meijers-Heijboer H, Verhoog L, Brekelmans C, et al: Prophylactic surgery in BRCA 1/2 mutation carriers: predictive factors and follow-up [abstract]. Am J Hum Genet. 1999, 65: 111-10.1086/302455.CrossRef Meijers-Heijboer H, Verhoog L, Brekelmans C, et al: Prophylactic surgery in BRCA 1/2 mutation carriers: predictive factors and follow-up [abstract]. Am J Hum Genet. 1999, 65: 111-10.1086/302455.CrossRef
50.
go back to reference Hartmann LC, Schaid DJ, Woods JE, et al: Efficacy of bilateral prophylactic mastectomy in women with a family history of breast cancer. N Engl J Med. 1999, 340: 77-84. 10.1056/NEJM199901143400201., This is the most commonly quoted reference to support the suggestion that prophylactic mastectomy reduces risk of breast cancer. The problem is that this study, of necessity, was retrospective and many women did not have genetic analysis performedCrossRefPubMed Hartmann LC, Schaid DJ, Woods JE, et al: Efficacy of bilateral prophylactic mastectomy in women with a family history of breast cancer. N Engl J Med. 1999, 340: 77-84. 10.1056/NEJM199901143400201., This is the most commonly quoted reference to support the suggestion that prophylactic mastectomy reduces risk of breast cancer. The problem is that this study, of necessity, was retrospective and many women did not have genetic analysis performedCrossRefPubMed
51.
go back to reference Daltrey IR, Eeles RA, Kissin MW: Bilateral prophylactic mastectomy: not just a woman's problem!. Breast. 1998, 7: 236-237. 10.1016/S0960-9776(98)90118-7.CrossRef Daltrey IR, Eeles RA, Kissin MW: Bilateral prophylactic mastectomy: not just a woman's problem!. Breast. 1998, 7: 236-237. 10.1016/S0960-9776(98)90118-7.CrossRef
52.
go back to reference Stefanek M, Enger C, Benkendorf J, Flamm-Honig S, Lerman C: Bilateral prophylactic mastectomy decision making: a vignette study. Prev Med. 1999, 29: 216-221. 10.1006/pmed.1999.0524.CrossRefPubMed Stefanek M, Enger C, Benkendorf J, Flamm-Honig S, Lerman C: Bilateral prophylactic mastectomy decision making: a vignette study. Prev Med. 1999, 29: 216-221. 10.1006/pmed.1999.0524.CrossRefPubMed
53.
go back to reference Brinton LA, Brown SL: Breast implants and cancer. J Natl Cancer Inst. 1997, 89: 1341-1349. 10.1093/jnci/89.18.1341.CrossRefPubMed Brinton LA, Brown SL: Breast implants and cancer. J Natl Cancer Inst. 1997, 89: 1341-1349. 10.1093/jnci/89.18.1341.CrossRefPubMed
54.
go back to reference Piver MS, Jishi MF, Tsukada Y, Nava G: Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian carcinoma. A report of the Gilda Radner Familial Ovarian Cancer Registry. Cancer. 1993, 71: 2751-55.CrossRefPubMed Piver MS, Jishi MF, Tsukada Y, Nava G: Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian carcinoma. A report of the Gilda Radner Familial Ovarian Cancer Registry. Cancer. 1993, 71: 2751-55.CrossRefPubMed
55.
go back to reference Breast Cancer Linkage Consortium: The pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet. 1997, 349: 1505-1510. 10.1016/S0140-6736(96)10109-4.CrossRef Breast Cancer Linkage Consortium: The pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet. 1997, 349: 1505-1510. 10.1016/S0140-6736(96)10109-4.CrossRef
56.
go back to reference Chappuis PO, Rosenblatt J, Foulkes WD: The influence of familial and hereditary factors on the prognosis of breast cancer. Ann Oncol. 1999, 10: 1163-1170. 10.1023/A:1008301314812., This reference summarizes the studies investigating survival differences in women who have breast cancer who are BRCA1/BRCA2 carriers versus sporadic casesCrossRefPubMed Chappuis PO, Rosenblatt J, Foulkes WD: The influence of familial and hereditary factors on the prognosis of breast cancer. Ann Oncol. 1999, 10: 1163-1170. 10.1023/A:1008301314812., This reference summarizes the studies investigating survival differences in women who have breast cancer who are BRCA1/BRCA2 carriers versus sporadic casesCrossRefPubMed
57.
go back to reference Verhoog LC, Brekelmans CT, Seynaeve C, et al: Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA 1. Lancet. 1998, 351: 316-321. 10.1016/S0140-6736(97)07065-7.CrossRefPubMed Verhoog LC, Brekelmans CT, Seynaeve C, et al: Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA 1. Lancet. 1998, 351: 316-321. 10.1016/S0140-6736(97)07065-7.CrossRefPubMed
58.
go back to reference Foulkes WD, Wong N, Brunet JS, et al: Germ-line BRCA 1 mutation is an adverse prognostic factor in Ashkenazi Jewish women with breast cancer. Clin Cancer Res. 1997, 3: 2465-2469.PubMed Foulkes WD, Wong N, Brunet JS, et al: Germ-line BRCA 1 mutation is an adverse prognostic factor in Ashkenazi Jewish women with breast cancer. Clin Cancer Res. 1997, 3: 2465-2469.PubMed
59.
go back to reference Lee JS, Wacholder S, Struewing JP, et al: Survival after breast cancer in Ashkenazi Jewish BRCA 1 and BRCA2 mutation carriers. J Natl Cancer Inst. 1999, 91: 259-263. 10.1093/jnci/91.3.259.CrossRefPubMed Lee JS, Wacholder S, Struewing JP, et al: Survival after breast cancer in Ashkenazi Jewish BRCA 1 and BRCA2 mutation carriers. J Natl Cancer Inst. 1999, 91: 259-263. 10.1093/jnci/91.3.259.CrossRefPubMed
60.
go back to reference Verhoog LC, Brekelmans CT, Seynaeve C, et al: Survival in hereditary breast cancer associated with germline mutations of BRCA 2. J Clin Oncol. 1999, 17: 3396-3402.PubMed Verhoog LC, Brekelmans CT, Seynaeve C, et al: Survival in hereditary breast cancer associated with germline mutations of BRCA 2. J Clin Oncol. 1999, 17: 3396-3402.PubMed
61.
go back to reference Early Breast Cancer Trialists' Collaborative Group : Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Lancet. 1992, 339: 71-85. 10.1016/0140-6736(92)90997-H. Early Breast Cancer Trialists' Collaborative Group : Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Lancet. 1992, 339: 71-85. 10.1016/0140-6736(92)90997-H.
62.
go back to reference Robson M, Gilewski T, Haas B, et al: BRCA -associated breast cancer in young women. J Clin Oncol. 1998, 16: 1642-1649.PubMed Robson M, Gilewski T, Haas B, et al: BRCA -associated breast cancer in young women. J Clin Oncol. 1998, 16: 1642-1649.PubMed
63.
go back to reference Cannistra SA: BRCA1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1254; discussion 1256-1257. 10.1056/NEJM199704243361713. Cannistra SA: BRCA1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1254; discussion 1256-1257. 10.1056/NEJM199704243361713.
64.
go back to reference Johannsson O, Ranstam J, Borg A, Olsson H: BRCA 1 mutations and survival in women with ovarian cancer. N Engl J Med. 1997, 336: 1255-1256; discussion 1256-1257. Johannsson O, Ranstam J, Borg A, Olsson H: BRCA 1 mutations and survival in women with ovarian cancer. N Engl J Med. 1997, 336: 1255-1256; discussion 1256-1257.
65.
go back to reference Whitmore SE: BRCA1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1254-1255; discussion 1256-1257. Whitmore SE: BRCA1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1254-1255; discussion 1256-1257.
66.
go back to reference Modan B: BRCA 1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1255; discussion 1256-1257. Modan B: BRCA 1 mutations and survival in women with ovarian cancer [letter]. N Engl J Med. 1997, 336: 1255; discussion 1256-1257.
67.
go back to reference Pharoah PD, Easton DF, Stockton DL, Gayther S, Ponder BA: Survival in familial, BRCA1-associated, and BRCA2-associated epithelial ovarian cancer. United Kingdom Coordinating Committee for Cancer Research (UKCCCR) Familial Ovarian Cancer Study Group. Cancer Res. 1999, 59: 868-871.PubMed Pharoah PD, Easton DF, Stockton DL, Gayther S, Ponder BA: Survival in familial, BRCA1-associated, and BRCA2-associated epithelial ovarian cancer. United Kingdom Coordinating Committee for Cancer Research (UKCCCR) Familial Ovarian Cancer Study Group. Cancer Res. 1999, 59: 868-871.PubMed
68.
go back to reference Shen SX, Weaver Z, Xu X, Li C, Weinstein M, Chen L, et al: A targeted disruption of the murine brca 1 gene causes gamma-irradiation hypersensitivity and genetic instability. Oncogene. 1998, 17: 3115-3124. 10.1038/sj.onc.1202243.CrossRefPubMed Shen SX, Weaver Z, Xu X, Li C, Weinstein M, Chen L, et al: A targeted disruption of the murine brca 1 gene causes gamma-irradiation hypersensitivity and genetic instability. Oncogene. 1998, 17: 3115-3124. 10.1038/sj.onc.1202243.CrossRefPubMed
69.
go back to reference Sharan SK, Morimatsu M, Albreicht U, et al: Embyronic lethality and radiation hypersensitivity mediated by Rad 51 in mice lacking brca 2. Nature. 1997, 386: 804-810. 10.1038/386804a0.CrossRefPubMed Sharan SK, Morimatsu M, Albreicht U, et al: Embyronic lethality and radiation hypersensitivity mediated by Rad 51 in mice lacking brca 2. Nature. 1997, 386: 804-810. 10.1038/386804a0.CrossRefPubMed
70.
go back to reference Coleman CN: Molecular biology in radiation oncology. Radiation oncology perspective of BRCA 1 and BRCA2. Acta Oncol. 1999, 38 (Suppl 13): 55-59. 10.1080/028418699432770.CrossRef Coleman CN: Molecular biology in radiation oncology. Radiation oncology perspective of BRCA 1 and BRCA2. Acta Oncol. 1999, 38 (Suppl 13): 55-59. 10.1080/028418699432770.CrossRef
71.
go back to reference Early Breast Cancer Trialists' Collaborative Group : Ovarian oblation in early breast cancer: overview of the randomised trials. Lancet. 1996, 348: 1189-1196. 10.1016/S0140-6736(96)05023-4.CrossRef Early Breast Cancer Trialists' Collaborative Group : Ovarian oblation in early breast cancer: overview of the randomised trials. Lancet. 1996, 348: 1189-1196. 10.1016/S0140-6736(96)05023-4.CrossRef
72.
go back to reference Frank TS, Manley SA, Olopade OI, et al: Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. J Clin Oncol. 1998, 16: 2417-2425.PubMed Frank TS, Manley SA, Olopade OI, et al: Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. J Clin Oncol. 1998, 16: 2417-2425.PubMed
Metadata
Title
Future possibilities in the prevention of breast cancer: Intervention strategies in BRCA1 and BRCA2 mutation carriers
Author
Rosalind A Eeles
Publication date
01-08-2000
Publisher
BioMed Central
Published in
Breast Cancer Research / Issue 4/2000
Electronic ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr70

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