A family history of breast cancer will not predict female early onset breast cancer in a population-based setting
详细信息    查看全文
  • 作者:Geertruida H de Bock (1) (2)
    Catharina E Jacobi (2)
    Caroline Seynaeve (3)
    Elly MM Krol-Warmerdam (4)
    Jannet Blom (3)
    Christi J van Asperen (5)
    Cees J Cornelisse (6)
    Jan GM Klijn (3)
    Peter Devilee (7)
    Rob AEM Tollenaar (4)
    Cecile TM Brekelmans (3)
    Johannes C van Houwelingen (8)
  • 刊名:BMC Cancer
  • 出版年:2008
  • 出版时间:December 2008
  • 年:2008
  • 卷:8
  • 期:1
  • 全文大小:533KB
  • 参考文献:1. Visser O, Coebergh JW, van Dijck JA, Siesling S: / Incidence of cancer in The Netherlands 1998. Tenth report of the Netherlands Cancer Registry Utrecht: Association of Comprehensive Cancer Centres 2002.
    2. Collaborative Group on Hormonal Factors in Breast Cancer: Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease. / Lancet 2001, 358: 1389-399. CrossRef
    3. Pharoah PD, Day NE, Duffy S, Easton DF, Ponder BA: Family history and the risk of breast cancer: a systematic review and meta-analysis. / Int J Cancer 1997, 71: 800-09. CrossRef
    4. Eccles DM, Evans DG, Mackay J: Guidelines for a genetic risk based approach to advising women with a family history of breast cancer. UK Cancer Family Study Group (UKCFSG). / J Med Genet 2000, 37: 203-09. jmg.37.3.203">CrossRef
    5. BASO Breast Specialty Group, Blamey RW: The British Association of Surgical Oncology guidelines for surgeons in the management of symptomatic breast disease in the UK (1998 revision). BASO Breast Specialty Group. / Eur J Surg Oncol 1998, 24: 464-76. CrossRef
    6. Hoskins KF, Stopfer JE, Calzone KA, / et al.: Assessment and counseling for women with a family history of breast cancer. A guide for clinicians. / JAMA 1995, 273: 577-85. jama.273.7.577">CrossRef
    7. Van Asperen CJ, De Bock GH, Horst F, De Koning HJ, Rutgers EJ: Screening for breast cancer on basis of individual risk assessment for women ineligible for the national population screening program. / Ned Tijdschr Geneeskd 2001, 145: 120-25.
    8. Lucassen A, Watson E, Harcourt J, Rose P, O'Grady J: Guidelines for referral to a regional genetics service: GPs respond by referring more appropriate cases. / Fam Pract 2001, 18: 135-40. CrossRef
    9. Nathanson KL, Wooster R, Weber BL: Breast cancer genetics: what we know and what we need. / Nat Med 2001, 7: 552-56. CrossRef
    10. Klein JP, Moeschberger ML: / Survival Analysis: Techniques for Censored and Truncated Data / 2 Edition NewYork:Springer-Verlag 2003.
    11. Claus EB, Risch N, Thompson WD: Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. / Cancer 1994, 73: 643-51. CrossRef
    12. Berry DA, Parmigiani G, Sanchez J, Schildkraut J, Winer E: Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history. / J Natl Cancer Inst 1997, 89: 227-38. jnci/89.3.227">CrossRef
    13. Parmigiani G, Berry D, Aguilar O: Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2. / Am J Hum Genet 1998, 62: 145-58. CrossRef
    14. Van Asperen CJ, Brohet RM, Meijers-Heijboer EJ, Hoogerbrugge N, Verhoef S, Vasen HF, Ausems MG, Menko FH, Gomez Garcia EB, Klijn JG, Hogervorst FB, van Houwelingen JC, van 't Veer LJ, Rookus MA, van Leeuwen FE, on behalf of the Netherlands Collaborative Group on Hereditary Breast Cancer (HEBON): Cancer risks in BRCA2 families: Estimates for sites other than breast and ovary. / J Med Genet 2005, 42: 711-19. jmg.2004.028829">CrossRef
    15. Eerola H, Blomqvist C, Pukkala E, Pyrhonen S, Nevanlinna H: Familial breast cancer in Southern Finland: how prevalent are breast cancer families and can we trust the family history reported by patients? / Eur J Cancer 2000, 36: 1143-148. CrossRef
    16. Ziogras A, Anton-Culver H: Validation of family history data in cancer family registries. / Am J Prev Med 2003, 24: 190-98. CrossRef
    17. Thompson D, Easton DF, Breast Cancer Linkage Consortium: Cancer Incidence in BRCA1 mutation carriers. / J Natl Cancer Inst 2002, 94: 1358-365.
    18. The Breast Cancer Linkage Consortium: Cancer risks in BRCA2 mutation carriers. / J Natl Cancer Inst 1999, 91: 1310-316. jnci/91.15.1310">CrossRef
    19. Eccles DM, Englefield P, Soulby MA, Campbell IG: BRCA1 mutations in Southern England. / Br J Cancer 1998, 77: 2199-203.
    20. Gershoni-Baruch R, Dagan E, Fried G, Kepten I, Robinson E: BRCA1 and BRCA2 founder mutations in patients with bilateral breast cancer. / Eur J Hum Genet 1999, 7: 833-36. j.ejhg.5200371">CrossRef
    21. Steinmann D, Bremer M, Rades D, / et al.: Mutations of the BRCA1 and BRCA2 genes in patients with bilateral breast cancer. / Br J Cancer 2001, 85: 850-58. joc.2001.2016">CrossRef
    22. Guttmacher AE, Collins FS, Carmona RH: The family history -more important than ever. / N Engl J Med 2004, 351: 2333-336. CrossRef
    23. Harrell FE Jr, Lee KL, Mark DB: Multivariable prognostic models: issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors. / Stat Med 1996, 15: 361-87. CrossRef
    24. Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE: Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. / Lancet 1994, 343: 692-95. CrossRef
    25. Claus EB, Risch N, Thompson WD: The calculation of breast cancer risk for women with a first degree family history of ovarian cancer. / Breast Cancer Res Treat 1993, 28: 115-120. CrossRef
    26. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/8/203/prepub
  • 作者单位:Geertruida H de Bock (1) (2)
    Catharina E Jacobi (2)
    Caroline Seynaeve (3)
    Elly MM Krol-Warmerdam (4)
    Jannet Blom (3)
    Christi J van Asperen (5)
    Cees J Cornelisse (6)
    Jan GM Klijn (3)
    Peter Devilee (7)
    Rob AEM Tollenaar (4)
    Cecile TM Brekelmans (3)
    Johannes C van Houwelingen (8)

    1. Department of Epidemiology, Groningen University Medical Center, Groningen, The Netherlands
    2. Department of Medical Decision Making, Leiden University Medical Center, Leiden, The Netherlands
    3. Department of Medical Oncology, Erasmus Medical Center-Dr Daniel den Hoed Cancer Center, Rotterdam, The Netherlands
    4. Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands
    5. Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
    6. Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands
    7. Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands
    8. Department of Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands
  • ISSN:1471-2407
文摘
Background An increased risk of breast cancer for relatives of breast cancer patients has been demonstrated in many studies, and having a relative diagnosed with breast cancer at an early age is an indication for breast cancer screening. This indication has been derived from estimates based on data from cancer-prone families or from BRCA1/2 mutation families, and might be biased because BRCA1/2 mutations explain only a small proportion of the familial clustering of breast cancer. The aim of the current study was to determine the predictive value of a family history of cancer with regard to early onset of female breast cancer in a population based setting. Methods An unselected sample of 1,987 women with and without breast cancer was studied with regard to the age of diagnosis of breast cancer. Results The risk of early-onset breast cancer was increased when there were: (1) at least 2 cases of female breast cancer in first-degree relatives (yes/no; HR at age 30: 3.09; 95% CI: 128-7.44), (2) at least 2 cases of female breast cancer in first or second-degree relatives under the age of 50 (yes/no; HR at age 30: 3.36; 95% CI: 1.12-0.08), (3) at least 1 case of female breast cancer under the age of 40 in a first- or second-degree relative (yes/no; HR at age 30: 2.06; 95% CI: 0.83-.12) and (4) any case of bilateral breast cancer (yes/no; HR at age 30: 3.47; 95%: 1.33-.05). The positive predictive value of having 2 or more of these characteristics was 13% for breast cancer before the age of 70, 11% for breast cancer before the age of 50, and 1% for breast cancer before the age of 30. Conclusion Applying family history related criteria in an unselected population could result in the screening of many women who will not develop breast cancer at an early age.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700