Prognosis and clinical presentation of BRCA2-associated breast cancer

被引:43
作者
Loman, N
Johannsson, A [1 ]
Bendahl, PO
Dahl, N
Einbeigi, Z
Gerdes, AM
Borg, Å
Olsson, H
机构
[1] Univ Lund Hosp, Dept Oncol, Jubileum Inst, SE-22185 Lund, Sweden
[2] Uppsala Univ, Akad Sjukhuset, Dept Clin Genet, Uppsala, Sweden
[3] Gothenburg Univ, Sahlgrens Univ Hosp, Dept Oncol, S-41124 Gothenburg, Sweden
[4] Odense Univ Hosp, Dept Clin Genet, DK-5000 Odense, Denmark
关键词
breast cancer; BRCA2; hereditary; prognosis; stage;
D O I
10.1016/S0959-8049(00)00098-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
54 female breast cancer patients from 22 families with BRCA2 germ line mutations from Sweden and Denmark were compared with 214 age- and date of diagnosis-matched controls identified among breast cancer patients from South Sweden. At diagnosis, BRCA2-associated cases were more often node-positive (N +). OR = 1.9 (95% confidence interval (CI)= 1.0-3.6; P = 0.036), and were more often clinical stage IV: OR = 4.6 (95% CI = 1.3-17; P = 0.021) than the controls. Bilateral disease was also more common among the BRCA2-associated cases: OR = 2.4 (95% CI = 1.1-5.3; P = 0.027). Breast cancer-specific survival (BCSS) was significantly worse among the BRCA2-associated cases: RR = 2.0 (95% CI = 1.2-3.4; P = 0.010). When stage was corrected for in a multivariate analysis, BCSS was no longer significantly worse for the BRCA2-associated cases: RR = 1.6 (95% CI = 0.85-3.1). The corresponding effect after correction for bilateral disease was: RR = 1.8 (95% CI = 1.0-3.1; P = 0.034). The unfavourable prognosis in BRCA2-associated breast cancer seems, to a great extent, to be a consequence of the higher clinical stage at diagnosis. The increased presence of bilateral cancers appears to have less impact on survival in this group of hereditary breast cancer. Data presented here needs to be taken into account when counselling healthy carriers of BRCA2 germ line mutations. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1365 / 1373
页数:9
相关论文
共 23 条
[1]   Inherited BRCA2 mutation associated with high grade breast cancer [J].
Agnarsson, BA ;
Jonasson, JG ;
Björnsdottir, IB ;
Barkardottir, RB ;
Egilsson, V ;
Sigurdsson, H .
BREAST CANCER RESEARCH AND TREATMENT, 1998, 47 (02) :121-127
[2]   Survival in early-onset BRCA1 breast-cancer patients [J].
Ansquer, Y ;
Gautier, C ;
Fourquet, A ;
Asselain, B ;
Stoppa-Lyonnet, D .
LANCET, 1998, 352 (9127) :541-541
[3]  
Armes JE, 1998, CANCER-AM CANCER SOC, V83, P2335, DOI 10.1002/(SICI)1097-0142(19981201)83:11<2335::AID-CNCR13>3.0.CO
[4]  
2-N
[5]  
Armes JE, 1999, CANCER RES, V59, P2011
[6]  
Foulkes WD, 1997, CLIN CANCER RES, V3, P2465
[7]  
Hakansson S, 1997, AM J HUM GENET, V60, P1068
[8]  
Hermanek P., 1987, TNM Classification of Malignant Tumors, V4th edn
[9]   Survival of BRCA1 breast and ovarian cancer patients:: A population-based study from southern Sweden [J].
Jóhannsson, OT ;
Ranstam, J ;
Borg, Å ;
Olsson, H .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :397-404
[10]   Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations [J].
Lakhani, SR ;
Jacquemier, J ;
Sloane, JP ;
Gusterson, BA ;
Anderson, TJ ;
van de Vijver, MJ ;
Farid, LM ;
Venter, D ;
Antoniou, A ;
Storfer-Isser, A ;
Smyth, E ;
Steel, CM ;
Haites, N ;
Scott, RJ ;
Goldgar, D ;
Neuhausen, S ;
Daly, PA ;
Ormiston, W ;
McManus, R ;
Scherneck, S ;
Ponder, BAJ ;
Ford, D ;
Peto, J ;
Stoppa-Lyonnet, D ;
Bignon, YJ ;
Struewing, JP ;
Spurr, NK ;
Bishop, DT ;
Klijn, JGM ;
Devilee, P ;
Cornelisse, CJ ;
Lasset, C ;
Lenoir, G ;
Barkardottir, RB ;
Egilsson, V ;
Hamann, U ;
Chang-Claude, J ;
Sobol, H ;
Weber, B ;
Stratton, MR ;
Easton, DF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (15) :1138-1145