Dissecting the Heterogeneity of Triple-Negative Breast Cancer

被引:374
作者
Metzger-Filho, Otto [1 ]
Tutt, Andrew [2 ]
de Azambuja, Evandro [1 ]
Saini, Kamal S. [1 ]
Viale, Giuseppe [5 ]
Loi, Sherene [1 ]
Bradbury, Ian [4 ]
Bliss, Judith M. [3 ]
Azim, Hatem A., Jr. [1 ]
Ellis, Paul [2 ]
Di Leo, Angelo [6 ]
Baselga, Jose [7 ]
Sotiriou, Christos [1 ]
Piccart-Gebhart, Martine [1 ]
机构
[1] Univ Libre Bruxelles, Inst Jules Bordet, B-1000 Brussels, Belgium
[2] Kings Coll London, London, England
[3] Inst Canc Res, Sutton, Surrey, England
[4] Frontier Sci, Kincraig, Scotland
[5] Univ Milan, European Inst Oncol, Milan, Italy
[6] Hosp Prato, Prato, Italy
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Boston, MA USA
关键词
INVASIVE DUCTAL CARCINOMA; BASAL-LIKE PHENOTYPE; ESTROGEN-RECEPTOR; SPORADIC BREAST; POLY(ADP-RIBOSE) POLYMERASE; MOLECULAR CHARACTERIZATION; EPITHELIAL PHENOTYPE; AFRICAN-AMERICAN; HORMONE-RECEPTOR; BRCA1; PROMOTER;
D O I
10.1200/JCO.2011.38.2010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) accounts for 15% to 20% of breast cancers. It is a heterogeneous disease, not only on the molecular level, but also on the pathologic and clinical levels. TNBC is associated with a significantly higher probability of relapse and poorer overall survival in the first few years after diagnosis when compared with other breast cancer subtypes. This is observed despite its usual high sensitivity to chemotherapy. In the advanced setting, responses observed with chemotherapy lack durability. Early-stage clinical studies suggested impressive potential when a poly (ADP-ribose) polymerase (PARP) inhibitor is given for the treatment of advanced TNBC with BRCA gene dysfunction. The molecular complexity of TNBC has led to proposed subclassifications, which will be of great value for the development of targeted therapies. In this review, we discuss the biology of TNBC at the pathologic and the molecular levels. We also elaborate on the role of systemic therapies and the results of the first phase III clinical trial evaluating the addition of iniparib, a novel investigational anticancer agent that does not possess characteristics typical of the PARP inhibitor class, in combination with chemotherapy in advanced TNBC. J Clin Oncol 30:1879-1887. (c) 2012 by American Society of Clinical Oncology
引用
收藏
页码:1879 / 1887
页数:9
相关论文
共 127 条
[1]  
Alba E, 2011, J CLIN ONCOL S, V29, p83s
[2]   Uncovering a Tumor Suppressor for Triple-Negative Breast Cancers [J].
Albeck, John G. ;
Brugge, Joan S. .
CELL, 2011, 144 (05) :638-640
[3]   The PARP superfamily [J].
Amé, JC ;
Spenlehauer, C ;
de Murcia, G .
BIOESSAYS, 2004, 26 (08) :882-893
[4]   Breast Carcinomas Arising at a Young Age: Unique Biology or a Surrogate for Aggressive Intrinsic Subtypes? [J].
Anders, Carey K. ;
Fan, Cheng ;
Parker, Joel S. ;
Carey, Lisa A. ;
Blackwell, Kimberly L. ;
Klauber-DeMore, Nancy ;
Perou, Charles M. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (01) :E18-E20
[5]  
[Anonymous], J CLIN ONCOL S
[6]  
[Anonymous], J CLIN ONCOL S
[7]   Placental cadherin and the basal epithelial phenotype of BRCA1-related breast cancer [J].
Arnes, JB ;
Brunet, JS ;
Stefansson, I ;
Bégin, LR ;
Wong, N ;
Chappuis, PO ;
Akslen, LA ;
Foulkes, WD .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :4003-4011
[8]   A synthetic lethal therapeutic approach: Poly(ADP) ribose polymerase inhibitors for the treatment of cancers deficient in DNA double-strand break repair [J].
Ashworth, Alan .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (22) :3785-3790
[9]  
Baselga J, 2010, ANN ONCOL S, V21, p8s
[10]   Descriptive analysis of estrogen receptor (ER)negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype - A population-based study from the California Cancer Registry [J].
Bauer, Katrina R. ;
Brown, Monica ;
Cress, Rosemary D. ;
Parise, Carol A. ;
Caggiano, Vincent .
CANCER, 2007, 109 (09) :1721-1728