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PMID: 22454417 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Dissecting the heterogeneity of triple-negative breast cancer.

Metzger-Filho O, Tutt A, de Azambuja E, Saini KS, Viale G, Loi S, Bradbury I, Bliss JM, Azim HA, Ellis P, Di Leo A, Baselga J, Sotiriou C, Piccart-Gebhart M

Abstract

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.

MeSH Terms
Antineoplastic Agents/therapeutic use Antineoplastic Combined Chemotherapy Protocols/therapeutic use Biomarkers, Tumor/analysis,genetics Breast Neoplasms/chemistry,classification,epidemiology,genetics,pathology,therapy Enzyme Inhibitors/therapeutic use Female Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Molecular Targeted Therapy Poly(ADP-ribose) Polymerase Inhibitors Prognosis Receptor, ErbB-2/analysis Receptors, Estrogen/analysis Receptors, Progesterone/analysis
Chemicals
Antineoplastic Agents Biomarkers, Tumor Enzyme Inhibitors Poly(ADP-ribose) Polymerase Inhibitors Receptors, Estrogen Receptors, Progesterone ERBB2 protein, human Receptor, ErbB-2
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Metzger-Filho Otto
Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Tutt Andrew
de Azambuja Evandro
Saini Kamal S
Viale Giuseppe
Loi Sherene
Bradbury Ian
Bliss Judith M
Azim Hatem A
Ellis Paul
Di Leo Angelo
Baselga José
Sotiriou Christos
Piccart-Gebhart Martine
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2012-05-20
Epub
2012-00-26
Pages
1879-87
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Grants
Cancer Research UK · 7741 · United Kingdom
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