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Published in: Breast Cancer Research 6/2003

Open Access 01-12-2003 | Research article

Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2mutation status

Authors: Niklas Loman, Anna Bladström, Oskar Johannsson, Åke Borg, Håkan Olsson

Published in: Breast Cancer Research | Issue 6/2003

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Abstract

Background

Relatives of breast cancer cases have an increased risk of the disease. The risk increases with increasing numbers and decreasing age of onset of affected relatives. In families with a BRCA1 or a BRCA2 mutation, individual carrier status predicts the risk of breast cancer. In relatives of cases where both BRCA1 and BRCA2 mutations are excluded, the risk remains undetermined.

Methods

Standardized incidence ratios (SIRs) and cumulative cancer incidences were calculated for relatives of a population-based set of early-onset breast cancer index cases (younger than age 41 years) with a defined BRCA mutation status (n = 203).

Results

In first-degree relatives (FDRs) of mutation-negative cases, breast cancer incidences (SIR = 2.3), prostate cancer incidences (SIR = 1.7), cervix cancer incidences (SIR = 3.3) and nonmelanoma skin cancer incidences (SIR = 2.8) were increased. The risks of breast cancer, prostate cancer and nonmelanoma skin cancer were further increased in FDRs of breast cancer cases younger than 36 years of age. In high-risk individuals with at least one relative with breast cancer apart from the index case, but no BRCA mutation in the family, breast cancer incidence was increased (SIR = 5.3); again the prostate cancer incidence was elevated (SIR = 2.5). The cumulative incidence of breast cancer at ages 50 and 70 years for FDRs of index cases without a BRCA mutation was 3.6% and 12.8%, respectively. Similarly, the cumulative incidence of breast cancer for high-risk women was 6.3% and 21.1% at ages 50 and 70 years, and that for FDRs of BRCA mutation carriers was 17.2% and 27.7% at the same ages.

Conclusion

The incidence of breast cancer is increased for FDRs of women with early-onset breast cancer irrespective of the BRCA status in the family. Risk increases with decreasing age and with increasing number of affected relatives. The incidences of prostate cancer, cervix cancer and nonmelanoma skin cancer are elevated for FDRs of early-onset breast cancer cases without a BRCA mutation, indicating a possible association between these cancers and early-onset breast cancer.
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Literature
1.
go back to reference Pharoah PDP, Day NE, Duffy S, Easton D, Ponder BAJ: Family history and risk of breast cancer: a systematic review and meta-analysis. Int J Cancer. 1997, 71: 800-809. 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.3.CO;2-R.CrossRefPubMed Pharoah PDP, Day NE, Duffy S, Easton D, Ponder BAJ: Family history and risk of breast cancer: a systematic review and meta-analysis. Int J Cancer. 1997, 71: 800-809. 10.1002/(SICI)1097-0215(19970529)71:5<800::AID-IJC18>3.3.CO;2-R.CrossRefPubMed
2.
go back to reference Andersson H, Bladström A, Olsson H, Möller TR: Familial breast and ovarian cancer: a Swedish population-based register study. Am J Epidemiol. 2000, 152: 1154-1163. 10.1093/aje/152.12.1154.CrossRef Andersson H, Bladström A, Olsson H, Möller TR: Familial breast and ovarian cancer: a Swedish population-based register study. Am J Epidemiol. 2000, 152: 1154-1163. 10.1093/aje/152.12.1154.CrossRef
3.
go back to reference Claus E, Risch N, Thompson W: Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. Cancer. 1994, 73: 643-651.CrossRefPubMed Claus E, Risch N, Thompson W: Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. Cancer. 1994, 73: 643-651.CrossRefPubMed
4.
go back to reference Gail MH, Brinton LA, Byar DP, Corle DK, Green SB, Schairer C, Mulvihill JJ: Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. J Natl Cancer Inst. 1989, 81: 1879-1886. 10.1093/jnci/81.24.1879.CrossRefPubMed Gail MH, Brinton LA, Byar DP, Corle DK, Green SB, Schairer C, Mulvihill JJ: Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. J Natl Cancer Inst. 1989, 81: 1879-1886. 10.1093/jnci/81.24.1879.CrossRefPubMed
5.
go back to reference Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994, 266: 66-71.CrossRefPubMed Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994, 266: 66-71.CrossRefPubMed
6.
go back to reference Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N, Gregory S, Gumbs C, Micklem G, Barfoot R, Hamoudi R, Patel S, Rice C, Biggs P, Hashim Y, Smith A, Connor F, Arason A, Gudmundsson J, Ficenec D, Kelsell D, Ford D, Tonin P, Bishop DT, Spurr NK, Ponder BAJ, Eeles R, Peto J, Devilee P, Cornelisse C, Lynch H, Narod S, Lenoir G, Egilsson V, Barkadottir RB, Easton DF, Bentley DR, Futreal PA, Ashworth A, Stratton MR: Identification of the breast cancer susceptibility gene BRCA2. Nature. 1995, 378: 789-792. 10.1038/378789a0.CrossRefPubMed Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N, Gregory S, Gumbs C, Micklem G, Barfoot R, Hamoudi R, Patel S, Rice C, Biggs P, Hashim Y, Smith A, Connor F, Arason A, Gudmundsson J, Ficenec D, Kelsell D, Ford D, Tonin P, Bishop DT, Spurr NK, Ponder BAJ, Eeles R, Peto J, Devilee P, Cornelisse C, Lynch H, Narod S, Lenoir G, Egilsson V, Barkadottir RB, Easton DF, Bentley DR, Futreal PA, Ashworth A, Stratton MR: Identification of the breast cancer susceptibility gene BRCA2. Nature. 1995, 378: 789-792. 10.1038/378789a0.CrossRefPubMed
7.
go back to reference Tavtigian SV, Simmard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S, Thorlacius S, Offit K, Stoppa-Lyonnet D, Belanger C, Bell R, Berry S, Bogden R, Chen Q, Davies T, Dumont M, Frye C, Hattier T, Jammulapati S, Janecki T, Jiang P, Kehrer R, Leblanc J-F, Mitchell JT, McArthur-Morrison J, Nguyen K, Peng Y, Samson C, Schroeder M, Snyder SC, Steele L, Stringfellow M, Stroup C, Swedlund B, Swensen J, Teng D, Thomas A, Tran T, Tranchant T, Weaver-Feldhaus J, Wong AKC, Shizuya H, Eyfjord JE, Cannon-Albright L, Labrie F, Skolnick MH, Weber B, Kamb A, Goldgar DE: The complete BRCA2 gene and mutations in chomosome13q linked kindreds. Nat Genet. 1996, 12: 333-337.CrossRefPubMed Tavtigian SV, Simmard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S, Thorlacius S, Offit K, Stoppa-Lyonnet D, Belanger C, Bell R, Berry S, Bogden R, Chen Q, Davies T, Dumont M, Frye C, Hattier T, Jammulapati S, Janecki T, Jiang P, Kehrer R, Leblanc J-F, Mitchell JT, McArthur-Morrison J, Nguyen K, Peng Y, Samson C, Schroeder M, Snyder SC, Steele L, Stringfellow M, Stroup C, Swedlund B, Swensen J, Teng D, Thomas A, Tran T, Tranchant T, Weaver-Feldhaus J, Wong AKC, Shizuya H, Eyfjord JE, Cannon-Albright L, Labrie F, Skolnick MH, Weber B, Kamb A, Goldgar DE: The complete BRCA2 gene and mutations in chomosome13q linked kindreds. Nat Genet. 1996, 12: 333-337.CrossRefPubMed
8.
go back to reference Dörum A, Heimdal K, Hovig E, Inganäs M, Möller P: Penetrance of BRCA1 1675delA and 1135 insA with respect to breast cancer and ovarian cancer. Am J Hum Genet. 1999, 65: 671-679. 10.1086/302530.CrossRefPubMedPubMedCentral Dörum A, Heimdal K, Hovig E, Inganäs M, Möller P: Penetrance of BRCA1 1675delA and 1135 insA with respect to breast cancer and ovarian cancer. Am J Hum Genet. 1999, 65: 671-679. 10.1086/302530.CrossRefPubMedPubMedCentral
9.
go back to reference Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE, Breast Cancer Linkage Consortium: Risks of cancer in BRCA1-mutation carriers. Lancet. 1994, 343: 692-695. 10.1016/S0140-6736(94)91578-4.CrossRefPubMed Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE, Breast Cancer Linkage Consortium: Risks of cancer in BRCA1-mutation carriers. Lancet. 1994, 343: 692-695. 10.1016/S0140-6736(94)91578-4.CrossRefPubMed
10.
go back to reference Goldgar DE, Neuhausen SL, Steele L, Fields P, Ward JH, Tran T, Ngyuen K, Stratton MR, Easton DF: A 45-year follow-up of kindred 107 and the search for BRCA2. J Natl Cancer Inst Monogr. 1995, 17: 15-19. Goldgar DE, Neuhausen SL, Steele L, Fields P, Ward JH, Tran T, Ngyuen K, Stratton MR, Easton DF: A 45-year follow-up of kindred 107 and the search for BRCA2. J Natl Cancer Inst Monogr. 1995, 17: 15-19.
11.
go back to reference Struewing JP, Hartge P, Wacholder S, Baker SM, Berlin M, McAdams M, Timmerman MM, Brody LC, Tucker MA: The risk of cancer associated with specific mutations of BRCA1 and BRCA2among Ashkenazi Jews. N Engl J Med. 1997, 336: 1401-1408. 10.1056/NEJM199705153362001.CrossRefPubMed Struewing JP, Hartge P, Wacholder S, Baker SM, Berlin M, McAdams M, Timmerman MM, Brody LC, Tucker MA: The risk of cancer associated with specific mutations of BRCA1 and BRCA2among 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, Olafsdottir GH, Sigvaldason H, Tryggvadottir L, Wacholder S, Tulinius H, Eyrfjörd JE: Population-basd study of risk of breast cancer in carriers of BRCA2 mutation. Lancet. 1998, 352: 1337-1339. 10.1016/S0140-6736(98)03300-5.CrossRefPubMed Thorlacius S, Struewing JP, Hartge P, Olafsdottir GH, Sigvaldason H, Tryggvadottir L, Wacholder S, Tulinius H, Eyrfjörd JE: Population-basd study of risk of breast cancer in carriers of BRCA2 mutation. Lancet. 1998, 352: 1337-1339. 10.1016/S0140-6736(98)03300-5.CrossRefPubMed
13.
go back to reference Hopper JL, Southey MC, Dite GS, Jolley DJ, Giles GG, McCredie MR, Easton DF, Venter DJ: Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study. Cancer Epidemiol Biomarkers Prev. 1999, 8: 741-747.PubMed Hopper JL, Southey MC, Dite GS, Jolley DJ, Giles GG, McCredie MR, Easton DF, Venter DJ: Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study. Cancer Epidemiol Biomarkers Prev. 1999, 8: 741-747.PubMed
14.
go back to reference Anglian Breast Cancer Study Group: Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Br J Cancer. 2000, 83: 1301-1308. 10.1054/bjoc.2000.1407.CrossRefPubMedCentral Anglian Breast Cancer Study Group: Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Br J Cancer. 2000, 83: 1301-1308. 10.1054/bjoc.2000.1407.CrossRefPubMedCentral
15.
go back to reference Antoniou A, Pharoah PDP, Narod S, Risch HA, Eyfjord JE, Hopper J, Loman N, Olsson H, Johansson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles D, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Tulinius H, Thorlacius S, Nevanlinna H, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF: Average risks of breast and ovarian cancer associated with mutations in BRCA1 or BRCA2 detected in case series unselected for family history: a combined analysis of 22 studies. Am Hum Genet. 2003, 75: 1117-1130. 10.1086/375033.CrossRef Antoniou A, Pharoah PDP, Narod S, Risch HA, Eyfjord JE, Hopper J, Loman N, Olsson H, Johansson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles D, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Tulinius H, Thorlacius S, Nevanlinna H, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF: Average risks of breast and ovarian cancer associated with mutations in BRCA1 or BRCA2 detected in case series unselected for family history: a combined analysis of 22 studies. Am Hum Genet. 2003, 75: 1117-1130. 10.1086/375033.CrossRef
16.
go back to reference Brose MS, Rebbeck TR, Calzone KA, Stopfer JE, Nathanson KL, Weber BL: Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. J Natl Cancer Inst. 2002, 94: 1365-1372. 10.1093/jnci/94.18.1365.CrossRefPubMed Brose MS, Rebbeck TR, Calzone KA, Stopfer JE, Nathanson KL, Weber BL: Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. J Natl Cancer Inst. 2002, 94: 1365-1372. 10.1093/jnci/94.18.1365.CrossRefPubMed
17.
go back to reference Huusko P, Gillanders E, Vahteristo P-S, Sarantaus L, Jou S, Kainu T, Rapakko K, Jones M, Markey C, Eerola H, Allinen M, Vehmanen P, Leisti J, Blanco G, Blomqvist C, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi O: Genome-wide scanning for linkage in Finnish breast cancer families [abstract]. Annual Meeting of the American Society of Human Genetics: San Diego. 2001, [http://www.faseb.org/genetics/ashg01/f149.htm] Huusko P, Gillanders E, Vahteristo P-S, Sarantaus L, Jou S, Kainu T, Rapakko K, Jones M, Markey C, Eerola H, Allinen M, Vehmanen P, Leisti J, Blanco G, Blomqvist C, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi O: Genome-wide scanning for linkage in Finnish breast cancer families [abstract]. Annual Meeting of the American Society of Human Genetics: San Diego. 2001, [http://​www.​faseb.​org/​genetics/​ashg01/​f149.​htm]
18.
go back to reference Zuppan P, Hall JM, Lee MK, Ponglikitmongkol M, King M-C: Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease. Am J Hum Genet. 1991, 48: 1065-1068.PubMedPubMedCentral Zuppan P, Hall JM, Lee MK, Ponglikitmongkol M, King M-C: Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease. Am J Hum Genet. 1991, 48: 1065-1068.PubMedPubMedCentral
19.
go back to reference Imbert A, Chaffanet M, Essioux L, Noguchi T, Adelaide J, Kerangueven F, Pasilier DL, Bonaiti-Pellie C, Sobol H, Birnboum D, Pebusque M: Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome. Genomics. 1996, 32: 29-32. 10.1006/geno.1996.0073.CrossRefPubMed Imbert A, Chaffanet M, Essioux L, Noguchi T, Adelaide J, Kerangueven F, Pasilier DL, Bonaiti-Pellie C, Sobol H, Birnboum D, Pebusque M: Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome. Genomics. 1996, 32: 29-32. 10.1006/geno.1996.0073.CrossRefPubMed
20.
go back to reference Seitz S, Rohde K, Bender E, Nothnagel A, Kolble K, Schlag P, Scherneck S: Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families. Oncogene. 1997, 14: 741-746. 10.1038/sj.onc.1200881.CrossRefPubMed Seitz S, Rohde K, Bender E, Nothnagel A, Kolble K, Schlag P, Scherneck S: Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families. Oncogene. 1997, 14: 741-746. 10.1038/sj.onc.1200881.CrossRefPubMed
21.
go back to reference Kainu T, Juo S, Desper R, Schaffer A, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi O, Tirkkonen M, Syrjakoski K, Kuukasjarvi T, Koivisto P, Karhu R, Holli K, Arason A, Johannesdottir G, Bergthorsson J, Johannsdottir H, Egilsson V, Barkardottir R, Johannsson O, Haraldsson K, Sandberg T, Holmberg E, Gronberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhonen S, Nevanlinna H: Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. Proc Natl Acad Sci USA. 2000, 97: 9603-9608. 10.1073/pnas.97.17.9603.CrossRefPubMedPubMedCentral Kainu T, Juo S, Desper R, Schaffer A, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi O, Tirkkonen M, Syrjakoski K, Kuukasjarvi T, Koivisto P, Karhu R, Holli K, Arason A, Johannesdottir G, Bergthorsson J, Johannsdottir H, Egilsson V, Barkardottir R, Johannsson O, Haraldsson K, Sandberg T, Holmberg E, Gronberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhonen S, Nevanlinna H: Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. Proc Natl Acad Sci USA. 2000, 97: 9603-9608. 10.1073/pnas.97.17.9603.CrossRefPubMedPubMedCentral
22.
go back to reference Sekine M, Nagata H, Tsuji S, Hirai Y, Fujimoto S, Hatae M, Kobayashi I, Fujii T, Ngata I, Ushijima K, Obata K, Suzuki M, Yoshinaga M, Umesaki H, Satoh S, Enomoto T, Motoyama S, Tanaka K: Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25. Hum Mol Genet. 2001, 10: 1421-1429. 10.1093/hmg/10.13.1421.CrossRefPubMed Sekine M, Nagata H, Tsuji S, Hirai Y, Fujimoto S, Hatae M, Kobayashi I, Fujii T, Ngata I, Ushijima K, Obata K, Suzuki M, Yoshinaga M, Umesaki H, Satoh S, Enomoto T, Motoyama S, Tanaka K: Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25. Hum Mol Genet. 2001, 10: 1421-1429. 10.1093/hmg/10.13.1421.CrossRefPubMed
23.
go back to reference Antoniou AC, Pharoah PDP, McMullan G, Day NE, Ponder BAJ, Easton D: Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study. Genet Epidemiol. 2001, 21: 1-18. 10.1002/gepi.1014.CrossRefPubMed Antoniou AC, Pharoah PDP, McMullan G, Day NE, Ponder BAJ, Easton D: Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study. Genet Epidemiol. 2001, 21: 1-18. 10.1002/gepi.1014.CrossRefPubMed
24.
go back to reference Loman N, Johannsson O, Kristoffersson U, Olsson H, Borg Å: Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. J Natl Cancer Inst. 2001, 93: 1215-1223. 10.1093/jnci/93.16.1215.CrossRefPubMed Loman N, Johannsson O, Kristoffersson U, Olsson H, Borg Å: Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. J Natl Cancer Inst. 2001, 93: 1215-1223. 10.1093/jnci/93.16.1215.CrossRefPubMed
25.
go back to reference StataCorp: Stata Statistical Software, release 6.0. College Station, TX: Stata Corporation. 1999 StataCorp: Stata Statistical Software, release 6.0. College Station, TX: Stata Corporation. 1999
26.
go back to reference Bratt O, Kristoffersson U, Lundgren R, Olsson H: The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer: a population-based cohort study. Eur J. 1997, 33: 2237-2240. 10.1016/S0959-8049(97)00320-1. Bratt O, Kristoffersson U, Lundgren R, Olsson H: The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer: a population-based cohort study. Eur J. 1997, 33: 2237-2240. 10.1016/S0959-8049(97)00320-1.
27.
go back to reference Kalish LA, McDougal WS, McKinlay JB: Family history and the risk of prostate cancer. Urology. 2000, 56: 803-806. 10.1016/S0090-4295(00)00780-9.CrossRefPubMed Kalish LA, McDougal WS, McKinlay JB: Family history and the risk of prostate cancer. Urology. 2000, 56: 803-806. 10.1016/S0090-4295(00)00780-9.CrossRefPubMed
28.
go back to reference Hayes RB, Liff JM, Pottern LM, Greenberg RS, Schoenberg JB, Schwartz AG, Swanson GM, Silverman DT, Brown LM, Hoover RN, Fraumeni JF: Prostate cancer risk in US blacks and whites with a family history of cancer. Int J Cancer. 1995, 60: 361-364.CrossRefPubMed Hayes RB, Liff JM, Pottern LM, Greenberg RS, Schoenberg JB, Schwartz AG, Swanson GM, Silverman DT, Brown LM, Hoover RN, Fraumeni JF: Prostate cancer risk in US blacks and whites with a family history of cancer. Int J Cancer. 1995, 60: 361-364.CrossRefPubMed
29.
go back to reference Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH: Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst. 1994, 86: 1600-1608.CrossRefPubMed Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH: Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst. 1994, 86: 1600-1608.CrossRefPubMed
30.
go back to reference Tulinius H, Egilsson V, Olafsdottir GH, Sigvaldason H: Risk of prostate, ovarian and endometrial cancer among relatives of women with breast cancer. BMJ. 1992, 305: 855-857.CrossRefPubMedPubMedCentral Tulinius H, Egilsson V, Olafsdottir GH, Sigvaldason H: Risk of prostate, ovarian and endometrial cancer among relatives of women with breast cancer. BMJ. 1992, 305: 855-857.CrossRefPubMedPubMedCentral
31.
go back to reference Breast Cancer Linkage Consortium: Cancer risk in BRCA2 mutation carriers. J Natl Cancer Inst. 1999, 91: 1310-1316. 10.1093/jnci/91.15.1310.CrossRef Breast Cancer Linkage Consortium: Cancer risk in BRCA2 mutation carriers. J Natl Cancer Inst. 1999, 91: 1310-1316. 10.1093/jnci/91.15.1310.CrossRef
32.
go back to reference Johannsson O, Loman N, Möller T, Kristoffersson U, Borg Å, Olsson H: Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers. Eur J Cancer. 1999, 35: 1248-1257. 10.1016/S0959-8049(99)00135-5.CrossRefPubMed Johannsson O, Loman N, Möller T, Kristoffersson U, Borg Å, Olsson H: Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers. Eur J Cancer. 1999, 35: 1248-1257. 10.1016/S0959-8049(99)00135-5.CrossRefPubMed
33.
go back to reference Thompson D, Easton D, Consortium BCL: Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. Am J Hum Genet. 2001, 68: 410-419. 10.1086/318181.CrossRefPubMedPubMedCentral Thompson D, Easton D, Consortium BCL: Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. Am J Hum Genet. 2001, 68: 410-419. 10.1086/318181.CrossRefPubMedPubMedCentral
34.
go back to reference Begg CB: On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst. 2002, 94: 1221-1226. 10.1093/jnci/94.16.1221.CrossRefPubMed Begg CB: On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst. 2002, 94: 1221-1226. 10.1093/jnci/94.16.1221.CrossRefPubMed
35.
go back to reference Antoniou AC, Gayther SA, Stratton JF, Ponder BA, Easton DF: Risk models for familial ovarian and breast cancer. Genet Epidemiol. 2000, 18: 173-190. 10.1002/(SICI)1098-2272(200002)18:2<173::AID-GEPI6>3.3.CO;2-I.CrossRefPubMed Antoniou AC, Gayther SA, Stratton JF, Ponder BA, Easton DF: Risk models for familial ovarian and breast cancer. Genet Epidemiol. 2000, 18: 173-190. 10.1002/(SICI)1098-2272(200002)18:2<173::AID-GEPI6>3.3.CO;2-I.CrossRefPubMed
36.
go back to reference Börresen A-L, Andersen TI, Garber J, Barbeier-Piraux N, Thorlacius S, Eyfjörd J, Ottestad L, Smith-Sörensen B, Holvig E, Malkin D, Friend SH: Screening for germline TP53 mutations in breast cancer patients. Cancer Res. 1992, 52: 3234-3236.PubMed Börresen A-L, Andersen TI, Garber J, Barbeier-Piraux N, Thorlacius S, Eyfjörd J, Ottestad L, Smith-Sörensen B, Holvig E, Malkin D, Friend SH: Screening for germline TP53 mutations in breast cancer patients. Cancer Res. 1992, 52: 3234-3236.PubMed
37.
go back to reference Prosser J, Porter D, Coles C, Thompson AM, Chetty U, Steel CM, Evans HJ: Constitutional p53 mutations in a non-Li–Fraumeni cancer family. Br J Cancer. 1992, 65: 527-528.CrossRefPubMedPubMedCentral Prosser J, Porter D, Coles C, Thompson AM, Chetty U, Steel CM, Evans HJ: Constitutional p53 mutations in a non-Li–Fraumeni cancer family. Br J Cancer. 1992, 65: 527-528.CrossRefPubMedPubMedCentral
38.
go back to reference Sidransky D, Tokino T, Helzlsouer K, Zehnbauer B, Rausch G, Shelton B, Prestigiacomo L, Vogelstein B, Davidson N: Inherited p53 gene mutations in breast cancer. Cancer Res. 1992, 52: 2984-2986.PubMed Sidransky D, Tokino T, Helzlsouer K, Zehnbauer B, Rausch G, Shelton B, Prestigiacomo L, Vogelstein B, Davidson N: Inherited p53 gene mutations in breast cancer. Cancer Res. 1992, 52: 2984-2986.PubMed
39.
go back to reference Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR: Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002, 31: 55-59. 10.1038/ng879.CrossRefPubMed Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR: Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002, 31: 55-59. 10.1038/ng879.CrossRefPubMed
40.
go back to reference Vahteristo P, Bartkova J, Eerola H, Syrjakoski K, Ojala S, Kilpivaara O, Tamminen A, Kononen J, Aittomaki K, Heikkila P, Holli K, Blomqvist C, Bartek J, Kallioniemi OP, Nevanlinna H: A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet. 2002, 71: 432-438. 10.1086/341943.CrossRefPubMedPubMedCentral Vahteristo P, Bartkova J, Eerola H, Syrjakoski K, Ojala S, Kilpivaara O, Tamminen A, Kononen J, Aittomaki K, Heikkila P, Holli K, Blomqvist C, Bartek J, Kallioniemi OP, Nevanlinna H: A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet. 2002, 71: 432-438. 10.1086/341943.CrossRefPubMedPubMedCentral
41.
go back to reference FitzGerald MG, Marsh DJ, Wahrer D, Bell D, Caron S, Shannon KE, Ishioka C, Isselbacher KJ, Garber JE, Eng C, Haber DA: Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer. Oncogene. 1998, 17: 727-731. 10.1038/sj.onc.1201984.CrossRefPubMed FitzGerald MG, Marsh DJ, Wahrer D, Bell D, Caron S, Shannon KE, Ishioka C, Isselbacher KJ, Garber JE, Eng C, Haber DA: Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer. Oncogene. 1998, 17: 727-731. 10.1038/sj.onc.1201984.CrossRefPubMed
42.
go back to reference Borg Å, Sandberg T, Nilsson K, Johannsson O, Klinker M, Måsbäck A, Westerdahl J, Olsson H, Ingvar C: High frequency of multiple melanomas and breast and pancreas carcinomnas in CDKN2A mutation-positive melanoma families. J Natl Cancer Inst. 2000, 92: 1260-1266. 10.1093/jnci/92.15.1260.CrossRefPubMed Borg Å, Sandberg T, Nilsson K, Johannsson O, Klinker M, Måsbäck A, Westerdahl J, Olsson H, Ingvar C: High frequency of multiple melanomas and breast and pancreas carcinomnas in CDKN2A mutation-positive melanoma families. J Natl Cancer Inst. 2000, 92: 1260-1266. 10.1093/jnci/92.15.1260.CrossRefPubMed
43.
go back to reference Hemminki A, Markie D, Thomlinson I, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Hoglund P, Jarvinen H, Kristo P, Pelin K, Ridanpaa M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen A, Stratton M, Chapelle Adl, Aaltonen L: A serine/threonine kinase gene defective in Peutz–Jeghers syndrome. Nature. 1998, 391: 184-187. 10.1038/34432.CrossRefPubMed Hemminki A, Markie D, Thomlinson I, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Hoglund P, Jarvinen H, Kristo P, Pelin K, Ridanpaa M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen A, Stratton M, Chapelle Adl, Aaltonen L: A serine/threonine kinase gene defective in Peutz–Jeghers syndrome. Nature. 1998, 391: 184-187. 10.1038/34432.CrossRefPubMed
45.
go back to reference Burdick D, Prior J: Peutz–Jeghers syndrom. A clinicopathologic study of a large family with a 27-year follow-up. Cancer. 1982, 50: 2139-2146.CrossRefPubMed Burdick D, Prior J: Peutz–Jeghers syndrom. A clinicopathologic study of a large family with a 27-year follow-up. Cancer. 1982, 50: 2139-2146.CrossRefPubMed
46.
go back to reference Thai TH, Du F, Tsan JT, Jin Y, Phung A, Spillman MA, Massa HF, Müller CY, Ashfaq R, Hathis JM, Miller DS, Trask BJ, Baer R, Bowcock AM: Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. Hum Mol Genet. 1998, 7: 195-202. 10.1093/hmg/7.2.195.CrossRefPubMed Thai TH, Du F, Tsan JT, Jin Y, Phung A, Spillman MA, Massa HF, Müller CY, Ashfaq R, Hathis JM, Miller DS, Trask BJ, Baer R, Bowcock AM: Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. Hum Mol Genet. 1998, 7: 195-202. 10.1093/hmg/7.2.195.CrossRefPubMed
47.
go back to reference Kato M, Yano K, Matsuo F, Saito H, Katagiri T, Kurumizaka H, Yoshimoto M, Kasumi F, Akiyama F, Sakamoto G, Nagawa H, Nakamura Y, Miki Y: Identification of Rad51 alteration in patients with bilateral breast cancer. J Hum Genet. 2000, 45: 133-137. 10.1007/s100380050199.CrossRefPubMed Kato M, Yano K, Matsuo F, Saito H, Katagiri T, Kurumizaka H, Yoshimoto M, Kasumi F, Akiyama F, Sakamoto G, Nagawa H, Nakamura Y, Miki Y: Identification of Rad51 alteration in patients with bilateral breast cancer. J Hum Genet. 2000, 45: 133-137. 10.1007/s100380050199.CrossRefPubMed
48.
go back to reference Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, Grossman S, Wahrer DC, Sgroi DC, Lane WS, Haber DA, Livingston DM: BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell. 2001, 105: 149-160.CrossRefPubMed Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, Grossman S, Wahrer DC, Sgroi DC, Lane WS, Haber DA, Livingston DM: BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell. 2001, 105: 149-160.CrossRefPubMed
49.
go back to reference Athma P, Rappaport R, Swift M: Molecular genotypingshows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet Cytogenet. 1996, 92: 130-134. 10.1016/S0165-4608(96)00328-7.CrossRefPubMed Athma P, Rappaport R, Swift M: Molecular genotypingshows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet Cytogenet. 1996, 92: 130-134. 10.1016/S0165-4608(96)00328-7.CrossRefPubMed
50.
go back to reference Keller G, Vogelsang H, Becker I, Hutter J, Ott K, Candidus S, Grundei T, Becker KF, Mueller J, Siewert JR, Hofler H: Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation. Am J. 1999, 155: 337-342. Keller G, Vogelsang H, Becker I, Hutter J, Ott K, Candidus S, Grundei T, Becker KF, Mueller J, Siewert JR, Hofler H: Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation. Am J. 1999, 155: 337-342.
51.
go back to reference Gayther S, Russel P, Harrington P, Antoniu A, Easton D, Ponder B: The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. Am J Hum Genet. 1999, 65: 1021-1029. 10.1086/302583.CrossRefPubMedPubMedCentral Gayther S, Russel P, Harrington P, Antoniu A, Easton D, Ponder B: The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. Am J Hum Genet. 1999, 65: 1021-1029. 10.1086/302583.CrossRefPubMedPubMedCentral
Metadata
Title
Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2mutation status
Authors
Niklas Loman
Anna Bladström
Oskar Johannsson
Åke Borg
Håkan Olsson
Publication date
01-12-2003
Publisher
BioMed Central
Published in
Breast Cancer Research / Issue 6/2003
Electronic ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr632

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