The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations.: A prospective study

被引:97
作者
Beiner, Mario E.
Finch, Amy
Rosen, Barry
Lubinski, Jan
Moller, Pal
Ghadirian, Parviz
Lynch, Henry T.
Friedman, Eitan
Sun, Ping
Narod, Steven A.
机构
[1] Ctr Res Womens Hlth, Toronto, ON M5G 1N8, Canada
[2] Univ Toronto, Dept Obstet & Gynecol, Div Gynecol Oncol, Toronto, ON M4X 1K9, Canada
[3] Princess Margaret Hosp, Div Gynecol Oncol, Toronto, ON M4X 1K9, Canada
[4] Pomeranian Med Univ, Szczecin, Poland
[5] Norwegian Radium Hosp, Dept Canc Genet, Oslo 3, Norway
[6] Univ Montreal, CHUM Hotel Dieu, Epidemiol Res Unit, Montreal, PQ H3C 3J7, Canada
[7] Creighton Univ, Sch Med, Dept Prevent Med & Publ Hlth, Omaha, NE 68178 USA
[8] Chaim Sheba Med Ctr, Oncogenet Unit, IL-52621 Tel Hashomer, Israel
关键词
endometrial cancer; BRCA1; BRCA2; association;
D O I
10.1016/j.ygyno.2006.08.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To evaluate the risk of endometrial cancer in women who carry a deleterious mutation in the BRCA1 or BRCA2 genes. Patients and methods. Women known to carry a BRCA1 or BRCA2 mutation, aged 45 to 70, were identified from an international registry and were followed prospectively. A total of 857 women completed a baseline questionnaire and one or more follow-up questionnaires. Study subjects were followed until diagnosis of endometrial cancer, ovarian cancer, death or the date of completion of the last questionnaire. The expected number of endometrial cancers was calculated using age and country-specific incidence rates. Results. After an average follow-up period of 3.3 years, six women were diagnosed with endometrial cancer, compared to 1.13 cancers expected (SIR = 5.3, p = 0.0011). Four of these six patients used tamoxifen in the past. The risk among women who were never exposed to tamoxifen treatment was not significantly elevated (SIR = 2.7, p = 0.17), but among the 226 participants who had used tamoxifen (220 as treatment and six for the primary prevention of breast cancer) the relative risk for endometrial cancer was 11.6 (p = 0.0004). Conclusion. The main contributor to the increased risk of endometrial cancer among BRCA carriers is tamoxifen treatment for a previous breast cancer. The risk and benefits of prophylactic hysterectomy should be discussed with women with a BRCA mutation considering tamoxifen therapy. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:7 / 10
页数:4
相关论文
共 19 条
[1]   Effects of conjugated, equine estrogen in postmenopausal women with hysterectomy - The women's health initiative randomized controlled trial [J].
Anderson, GL ;
Limacher, M ;
Assaf, AR ;
Bassford, T ;
Beresford, SAA ;
Black, H ;
Bonds, D ;
Brunner, R ;
Brzyski, R ;
Caan, B ;
Chlebowski, R ;
Curb, D ;
Gass, M ;
Hays, J ;
Heiss, G ;
Hendrix, S ;
Howard, BV ;
Hsia, J ;
Hubbell, A ;
Jackson, R ;
Johnson, KC ;
Judd, H ;
Kotchen, JM ;
Kuller, L ;
LaCroix, AZ ;
Lane, D ;
Langer, RD ;
Lasser, N ;
Lewis, CE ;
Manson, J ;
Margolis, K ;
Ockene, J ;
O'Sullivan, MJ ;
Phillips, L ;
Prentice, RL ;
Ritenbaugh, C ;
Robbins, J ;
Rossouw, JE ;
Sarto, G ;
Stefanick, ML ;
Van Horn, L ;
Wactawski-Wende, J ;
Wallace, R ;
Wassertheil-Smoller, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (14) :1701-1712
[2]  
[Anonymous], 1999, J NATL CANC I, V91, P1310
[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]  
Brose MS, 2002, J NATL CANCER I, V94, P1365, DOI 10.1093/jnci/94.18.1365
[5]   BRCA-mutation-associated fallopian tube carcinoma - A distinct clinical phenotype? [J].
Cass, R ;
Holschneider, C ;
Datta, N ;
Barbuto, D ;
Walts, AE ;
Karlan, BY .
OBSTETRICS AND GYNECOLOGY, 2005, 106 (06) :1327-1334
[6]   Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families [J].
Ford, D ;
Easton, DF ;
Stratton, M ;
Narod, S ;
Goldgar, D ;
Devilee, P ;
Bishop, DT ;
Weber, B ;
Lenoir, G ;
Chang-Claude, J ;
Sobol, H ;
Teare, MD ;
Struewing, J ;
Arason, A ;
Scherneck, S ;
Peto, J ;
Rebbeck, TR ;
Tonin, P ;
Neuhausen, S ;
Barkardottir, R ;
Eyfjord, J ;
Lynch, H ;
Ponder, BAJ ;
Gayther, SA ;
Birch, JM ;
Lindblom, A ;
Stoppa-Lyonnet, D ;
Bignon, Y ;
Borg, A ;
Hamann, U ;
Haites, N ;
Scott, RJ ;
Maugard, CM ;
Vasen, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) :676-689
[7]   Is uterine papillary serous adenocarcinoma a manifestation of the hereditary breast-ovarian cancer syndrome? [J].
Goshen, R ;
Chu, W ;
Elit, L ;
Pal, T ;
Hakimi, J ;
Ackerman, I ;
Fyles, A ;
Mitchell, M ;
Narod, SA .
GYNECOLOGIC ONCOLOGY, 2000, 79 (03) :477-481
[8]   HORMONE REPLACEMENT THERAPY AND ENDOMETRIAL CANCER RISK - A METAANALYSIS [J].
GRADY, D ;
GEBRETSADIK, T ;
KERLIKOWSKE, K ;
ERNSTER, V ;
PETITTI, D .
OBSTETRICS AND GYNECOLOGY, 1995, 85 (02) :304-313
[9]   BRCA2 germline mutation in a woman with uterine serous papillary carcinoma - Case report [J].
Lavie, O ;
Ben-Arie, A ;
Pilip, A ;
Rennert, G ;
Cohen, Y ;
Feiner, B ;
Auslnader, R .
GYNECOLOGIC ONCOLOGY, 2005, 99 (02) :486-488
[10]   BRCA germline mutations in Jewish women with uterine serous papillary carcinoma [J].
Lavie, O ;
Hornreich, G ;
Ben-Arie, A ;
Rennert, G ;
Cohen, Y ;
Keidar, R ;
Sagi, S ;
Lahad, EL ;
Auslander, R ;
Beller, U .
GYNECOLOGIC ONCOLOGY, 2004, 92 (02) :521-524