Pregnancies, breast-feeding, and breast cancer risk in the international BRCA1/2 carrier cohort study (IBCCS)

被引:149
作者
Andrieu, Nadine
Goldgar, David E.
Easton, Douglas F.
Rookus, Matti
Brohet, Richard
Antoniou, Antonis C.
Peock, Susan
Evans, Gareth
Eccles, Diana
Douglas, Fiona
Nogues, Catherine
Gauthier-Villars, Marion
Chompret, Agnes
van Leeuwen, Flora E.
Kluijt, Irina
Benitez, Javier
Arver, Brita
Olah, Edith
Chang-Claude, Jenny
机构
[1] Inst Curie, Serv Biostat, INSERM, F-75248 Paris 05, France
[2] Int Agcy Res Canc, F-69372 Lyon, France
[3] Univ Cambridge, Canc Res UK, Genet Epidemiol Unit, Dept Publ Hlth & Primary Care, Cambridge, England
[4] Netherlands Canc Inst, Dept Epidemiol, Amsterdam, Netherlands
[5] Manchester Reg Genet Serv, Manchester, Lancs, England
[6] Wessex Clin Genet Serv, Southampton, Hants, England
[7] No Clin Genet Serv, Newcastle Upon Tyne, Tyne & Wear, England
[8] Ctr Rene Huguenin, St Cloud, France
[9] Inst Curie, Serv Oncogenet, Paris, France
[10] Inst Gustave Roussy, Villejuif, France
[11] Ctr Nacl Invest Oncol, Dept Human Genet, Madrid, Spain
[12] Karolinska Univ Hosp, Radiumhemmet, Stockholm, Sweden
[13] Natl Inst Oncol, Budapest, Hungary
[14] German Canc Res Ctr, Div Clin Epidemiol, Heidelberg, Germany
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2006年 / 98卷 / 08期
关键词
D O I
10.1093/jnci/djj132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiparity, young age at first childbirth, and breast-feeding are associated with a reduced risk of breast cancer in the general population. The breast cancer predisposition gene, BRCA1, regulates normal cell differentiation. Because mammary gland cells divide and differentiate during pregnancy, reproductive factors may influence breast cancer risk in BRCA1/2 mutation carriers differently than they do in noncarriers. Methods: We performed a retrospective cohort study of 1601 women in the International BRCA1/2 Carrier Cohort Study cohort, all of whom carried a mutation in BRCA1 or BRCA2. Information on reproductive factors was obtained from a questionnaire. At the time of interview 853 subjects were classified with breast cancer. Data were analyzed by using a weighted cohort approach. All statistical tests were two-sided. Results: There was no statistically significant difference in the risk of breast cancer between parous and nulliparous women. Among parous women, an increasing number of full-term pregnancies was associated with a statistically significant decrease in the risk of breast cancer (P-trend =.008); risk was reduced by 14% (95% confidence interval [CI] = 6% to 22%) for each additional birth. This association was the same for carriers of mutations in either BRCA1 or BRCA2 and was restricted to women older than 40 years. In BRCA2 mutation carriers, first childbirth at later ages was associated with an increased risk of breast cancer compared with first childbirth before age 20 years (20-24 years, hazard ratio [HR] = 2.33 [95% CI = 0.93 to 5.83]; 25-29 years, HR = 2.68 [95% CI 1.02 to 7.07]; 30 years, HR = 1.97 [95% CI = 0.67 to 5.81]), whereas in BRCA1 mutation carriers, first childbirth at age 30 years or later was associated with a reduced risk of breast cancer compared with first childbirth before age 20 years (HR = 0.58 [95% CI = 0.36 to 0.94]). Neither history of interrupted pregnancies (induced abortions or miscarriage) nor history of breast-feeding was statistically significantly associated with the risk of breast cancer. Conclusions: BRCA1 and BRCA2 mutation carriers older than 40 years show a similar reduction in breast cancer risk with increasing parity as non-carriers.
引用
收藏
页码:535 / 544
页数:10
相关论文
共 41 条
[1]   THE SHORT-TERM AND LONG-TERM EFFECT OF A PREGNANCY ON BREAST-CANCER RISK - A PROSPECTIVE-STUDY OF 802,457 PAROUS NORWEGIAN WOMEN [J].
ALBREKTSEN, G ;
HEUCH, I ;
KVALE, G .
BRITISH JOURNAL OF CANCER, 1995, 72 (02) :480-484
[2]  
[Anonymous], IARC CANC BASE
[3]   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 [J].
Antoniou, A ;
Pharoah, PDP ;
Narod, S ;
Risch, HA ;
Eyfjord, JE ;
Hopper, JL ;
Loman, N ;
Olsson, H ;
Johannsson, O ;
Borg, Å ;
Pasini, B ;
Radice, P ;
Manoukian, S ;
Eccles, DM ;
Tang, N ;
Olah, E ;
Anton-Culver, H ;
Warner, E ;
Lubinski, J ;
Gronwald, J ;
Gorski, B ;
Tulinius, H ;
Thorlacius, S ;
Eerola, H ;
Nevanlinna, H ;
Syrjäkoski, K ;
Kallioniemi, OP ;
Thompson, D ;
Evans, C ;
Peto, J ;
Lalloo, F ;
Evans, DG ;
Easton, DF .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) :1117-1130
[4]   A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes [J].
Antoniou, AC ;
Goldgar, DE ;
Andrieu, N ;
Chang-Claude, J ;
Brohet, R ;
Rookus, MA ;
Easton, DF .
GENETIC EPIDEMIOLOGY, 2005, 29 (01) :1-11
[5]  
Begg CB, 2002, J NATL CANCER I, V94, P1221
[6]  
Beral V, 2004, LANCET, V363, P1007, DOI 10.1016/S0140-6736(04)15835-2
[7]   Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G ;
La Vecchia, C ;
Magnusson, C ;
Miller, T ;
Peterson, B ;
Pike, M ;
Thomas, D ;
van Leeuwen, F .
LANCET, 2002, 360 (9328) :187-195
[8]   CHILDBEARING, ORAL-CONTRACEPTIVE USE, AND BREAST-CANCER [J].
BERAL, V ;
REEVES, G .
LANCET, 1993, 341 (8852) :1102-1102
[9]   Prepubertal estradiol and genistein exposures up-regulate BRCA1 mRNA and reduce mammary tumorigenesis [J].
Cabanes, A ;
Wang, M ;
Olivo, S ;
DeAssis, S ;
Gustafsson, JÅ ;
Khan, G ;
Hilakivi-Clarke, L .
CARCINOGENESIS, 2004, 25 (05) :741-748
[10]   Modifying effect of reproductive risk factors on the age at onset of breast cancer for German BRCA1 mutation carriers [J].
ChangClaude, J ;
Becher, H ;
Eby, N ;
Bastert, G ;
Wahrendorf, J ;
Hamann, U .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1997, 123 (05) :272-279