Ten-year multi-institutional results of breast-conserving surgery and radiotherapy in BRCA1/2-associated stage I/II breast cancer

被引:251
作者
Pierce, LJ
Levin, AM
Rebbeck, TR
Ben-David, MA
Friedman, E
Solin, LJ
Harris, EE
Gaffney, DK
Haffty, BG
Dawson, LA
Narod, SA
Olivotto, IA
Eisen, A
Whelan, TJ
Olopade, OI
Isaacs, C
Merajver, SD
Wong, JS
Garber, JE
Weber, BL
机构
[1] Univ Michigan, Sch Med, Dept Radiat Oncol, Canc & Geriatr Ctr 4308, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48109 USA
[3] Univ Penn, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[4] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[6] Univ Utah, Sch Med, Salt Lake City, UT USA
[7] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, New Brunswick, NJ USA
[8] Georgetown Univ, Lombardi Canc Ctr, Washington, DC USA
[9] Harvard Univ, Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Univ Chicago, Sch Med, Chicago, IL 60637 USA
[11] Univ Toronto, Princess Margaret Hosp, Toronto, ON, Canada
[12] Hamilton Reg Canc Ctr, Hamilton, ON L8V 1C3, Canada
[13] British Columbia Canc Agcy, Victoria, BC, Canada
[14] Chaim Sheba Med Ctr, Ramat Gan, Israel
关键词
D O I
10.1200/JCO.2005.02.7888
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We compared the outcome of breast-conserving surgery and radiotherapy in BRCA1/2 mutation carriers with breast cancer versus that of matched sporadic controls. Methods A total of 160 BRCA 712 mutation carriers with breast cancer were matched with 445 controls with sporadic breast cancer. Primary end points were rates of in-breast tumor recurrence (IBTR) and contralateral breast cancers (CBCs). Median follow-up was 7.9 years for mutation carriers and 6.7 years for controls. Results There was no significant difference in IBTR overall between carriers and controls; 10- and 15-year; estimates were 12% and 24% for carriers and 9% and 17% for controls, respectively (hazard ratio [HR], 1.37; P = .19). Multivariate analyses for IBTR found BRCA1/2 mutation status to be an independent predictor of IBTR when carriers who had undergone cophorectomy were removed from analysis (HR, 1.99; P = .04); the incidence of IBTR in carriers who had undergone oophorectomy was not significantly different from that in sporadic controls (P = .37). CBCs were significantly greater in carriers versus controls, with 10- and 15-year estimates of 26% and 39%. for carriers and 3% and 7% for controls, respectively (HR, 10.43; P < .0001). Tamoxifen use significantly reduced risk of CBCs in mutation carriers (HR, 0.31; P = .05). Conclusion IBTR risk at 10 years is similar in BRCA1/2 carriers treated with breast conservation surgery who undergo oophorectomy versus sporadic controls. As expected, CBCs are significantly increased in carriers. Although the incidence of CBCs was significantly reduced in mutation carriers who this rate remained significantly greater than in controls. Additional strategies received tamoxifen, are needed to reduce contralateral cancers in these high-risk women.
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页码:2437 / 2443
页数:7
相关论文
共 24 条
[1]   BRCA1 and BRCA2:: From molecular genetics to clinical medicine [J].
Blackwood, MA ;
Weber, BL .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (05) :1969-1977
[2]   BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer [J].
Couch, FJ ;
DeShano, ML ;
Blackwood, MA ;
Calzone, K ;
Stopfer, J ;
Campeau, L ;
Ganguly, A ;
Rebbeck, T ;
Weber, BL ;
Jablon, L ;
Cobleigh, MA ;
Hoskins, K ;
Garber, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (20) :1409-1415
[3]   THE GENETIC EPIDEMIOLOGY OF BRCA1 [J].
EASTON, DF ;
NAROD, SA ;
FORD, D ;
STEEL, M .
LANCET, 1994, 344 (8924) :761-761
[4]   Familial breast cancer: An investigation into the outcome of treatment for early stage disease [J].
Eccles D. ;
Simmonds P. ;
Goddard J. ;
Coultas M. ;
Hodgson S. ;
Lalloo F. ;
Evans G. ;
Haites N. .
Familial Cancer, 2001, 1 (2) :65-72
[5]   Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer [J].
Fisher, B ;
Anderson, S ;
Bryant, J ;
Margolese, RG ;
Deutsch, M ;
Fisher, ER ;
Jeong, J ;
Wolmark, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (16) :1233-1241
[6]   Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2:: Analysis of 10,000 individuals [J].
Frank, TS ;
Deffenbaugh, AM ;
Reid, JE ;
Hulick, M ;
Ward, BE ;
Lingenfelter, B ;
Gumpper, KL ;
Scholl, T ;
Tavtigian, SV ;
Pruss, DR ;
Critchfield, GC .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1480-1490
[7]  
Gooley TA, 1999, STAT MED, V18, P695, DOI 10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.0.CO
[8]  
2-O
[9]   Outcome of conservatively managed early-onset breast cancer by BRCA1/2 status [J].
Haffty, BG ;
Harrold, E ;
Khan, AJ ;
Pathare, P ;
Smith, TE ;
Turner, BC ;
Glazer, PM ;
Ward, B ;
Carter, D ;
Matloff, E ;
Bale, AE ;
Alvarez-Franco, M .
LANCET, 2002, 359 (9316) :1471-1477
[10]  
Hart P.M., 2001, Handbook of industrial, work and organizational psychology, V2, P93