Prognostic role of BRCA1 mutation in patients with triple-negative breast cancer

被引:23
|
作者
Maksimenko, Jelena [1 ]
Irmejs, Arvids [1 ]
Nakazawa-Miklasevica, Miki [1 ]
Melbarde-Gorkusa, Inga [1 ]
Trofimovics, Genadijs [1 ]
Gardovskis, Janis [1 ]
Miklasevics, Edvins [1 ]
机构
[1] Riga Stradins Univ, Inst Oncol, LV-1012 Riga, Latvia
关键词
OVARIAN-CANCER; CARCINOMA; POPULATION; PHENOTYPE; SURVIVAL; SUBTYPES; BASAL; CHEMOSENSITIVITY; IDENTIFICATION; EXPRESSION;
D O I
10.3892/ol.2013.1684
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) is proposed to be an immunohistochemical surrogate of the basal-like breast cancer subtype. In spite of the relative chemosensitivity of this cancer subtype, it is characterized by aggressive clinical behavior; therefore, a further subclassification of TNBC is required to develop new targeted treatment. In previous studies, a strong correlation between BRCA1 mutation-associated tumors and TNBC has been identified. The aim of the present study was to investigate the prognostic significance of carrying two germline BRCA1 founder mutations (4153delA and 5382insC) in patients with TNBC in the Latvian population. A total of 78 consecutive BRCA1 mutation-negative and 38 BRCA1 mutation-positive invasive TNBC patients in stage I-IV with no history of ovarian or other primary advanced cancers, who had undergone definitive surgery and genetic testing between 2005 and 2011, were deemed eligible for study. Relapse rates and breast cancer-specific survival (BCS) outcomes were compared between mutation carriers and non-carriers. Univariate and multivariate analyses Cox proportional-hazards models were used to compute independent predictors of survival outcomes. No statistically significant differences were identified in relation to tumor size, T stage, stage, Ki-67 status and tumor differentiation grade between the two groups. The median follow-up period was 36 months for mutation carriers and 41 months for non-carriers. A higher proportion of BRCA1 mutation non-carriers experienced distant recurrence compared with that of mutation carriers (P<0.03). BRCA1 mutation carriers had a significantly higher BCS than non-carriers (94.9 vs. 76.9%; P<0.02). In the univariate analyses, BRCA1-positive status was associated with decreased risk of distant recurrence (HR, 0.228; 95% Cl, 0.052-0.997; P<0.049) and breast cancer-specific mortality (HR, 0.209; 95% Cl, 0.048-0.902; P<0.036). In the multivariate analysis Cox proportional-hazards model, BRCA1-positive status was an independent favorable prognostic factor for distant recurrence-free survival (HR, 3.301; 95% Cl, 1.102-9.893; P<0.033). In conclusion, results of the present study demonstrate that positive BRCA1 founder mutation status in TNBC, with no evidence of ovarian or other cancer type in advanced stage, significantly improves prognosis.
引用
收藏
页码:278 / 284
页数:7
相关论文
共 50 条
  • [1] BRCA1 MUTATION AND ITS PROGNOSTIC ROLE IN THE TRIPLE-NEGATIVE BREAST CANCER (TNBC) SUBTYPE
    Maksimenko, J. J.
    Irmejs, A.
    Trofimovics, G.
    Miklasevics, E.
    [J]. BREAST, 2013, 22 : S32 - S33
  • [2] Transcriptoma analyses in triple-negative breast cancer with BRCA1 germline mutation
    Nakamura, Kivvi Duarte
    Ferreira, Elisa
    Ramalho, Rodrigo
    Brianese, Rafael
    Carraro, Dirce
    [J]. CANCER RESEARCH, 2017, 77
  • [3] BRCA1 methylation in triple-negative breast cancer
    Kawachi, A.
    Okochi-Takada, E.
    Shimoi, T.
    Shimomura, A.
    Kodaira, M.
    Yunokawa, M.
    Yonemori, K.
    Shimizu, C.
    Fujiwara, Y.
    Ushijima, T.
    Tamura, K.
    [J]. ANNALS OF ONCOLOGY, 2015, 26 : 28 - 29
  • [4] BRCA1 testing for triple-negative breast cancer
    Bennet, Neil
    [J]. LANCET ONCOLOGY, 2012, 13 (04): : E143 - E143
  • [5] Evaluation of BRCA1/2 mutation prevalence in Korean women with triple-negative breast cancer
    Lee, A. S.
    Kang, E. Y.
    Baek, H.
    Chae, S.
    Kim, E-K.
    Kim, S. W.
    [J]. ANNALS OF ONCOLOGY, 2015, 26 : 16 - 16
  • [6] BRCA1 mutation in the Triple- Negative Breast Cancer Group
    Jelena Maksimenko
    Arvids Irmejs
    Genadijs Trofimovics
    Edvins Miklasevics
    [J]. Hereditary Cancer in Clinical Practice, 10 (Suppl 4)
  • [7] Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer
    Wong-Brown, Michelle W.
    Meldrum, Cliff J.
    Carpenter, Jane E.
    Clarke, Christine L.
    Narod, Steven A.
    Jakubowska, Anna
    Rudnicka, Helena
    Lubinski, Jan
    Scott, Rodney J.
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2015, 150 (01) : 71 - 80
  • [8] Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer
    Michelle W. Wong-Brown
    Cliff J. Meldrum
    Jane E. Carpenter
    Christine L. Clarke
    Steven A. Narod
    Anna Jakubowska
    Helena Rudnicka
    Jan Lubinski
    Rodney J. Scott
    [J]. Breast Cancer Research and Treatment, 2015, 150 : 71 - 80
  • [9] BRCA1 mutation is strongly associated with a triple negative phenotype in breast cancer patients
    Cordoba, O.
    Rubio, I.
    Xercavins, J.
    Diez, O.
    Alvarez, M.
    Cortadellas, T.
    Balmana, J.
    [J]. EJC SUPPLEMENTS, 2010, 8 (03): : 108 - 108
  • [10] BRCA1/2 mutation prevalence in triple-negative breast cancer patients without family history of breast and ovarian cancer.
    Rhiem, Kerstin
    Engel, Christoph
    Engel, Jutta
    Niederacher, Dieter
    Sutter, Christian
    Varon-Mateeva, Raymonda
    Steinemann, Doris
    Arnold, Norbert
    Dworniczak, Bernd
    Wang-Gohrke, Shan
    Gehrig, Andrea
    Wappenschmidt, Barbara
    Meindl, Alfons
    Schmutzler, Rita K.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)