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Clinical correlates of 'BRCAness' in triple-negative breast cancer of patients receiving adjuvant chemotherapy.

A M M Oonk ,
C van Rijn ,
M M Smits ,
L Mulder ,
N Laddach ,
S P Savola ,
J Wesseling ,
S Rodenhuis ,
A L T Imholz ,
E H Lips

Abstract

PATIENTS AND METHODS

DNA was isolated and BRCA1-like status was assessed in 101 patients with early-stage TNBC receiving adjuvant cyclophosphamide-based chemotherapy. Clinical characteristics and survival were compared between BRCA1-like and non-BRCA1-like groups. Results Sixty-six tumors (65%) had a BRCA1-like profile. Patients with BRCA1-like tumors tended to be younger and had more often node-negative disease (P = 0.06 and P = 0.03, respectively). Five-year recurrence-free survival was 80% for the BRCA1-like group and 75% for the non-BRCA1-like group (P = 0.35). T stage was the only variable significantly associated with survival.

CONCLUSIONS

BRCA1-like tumors share clinical features, like young age at diagnosis and similar nodal status, with breast cancers in BRCA1 mutation carriers. Their prognosis is similar to that of non-BRCA1-like tumors when conventional-dose chemotherapy is administered. TNBCs that are classified as BRCA1-like may contain a defect in homologous recombination and could, in theory, benefit from the addition of poly ADP ribose polymerase inhibitors.

BACKGROUND

We have previously reported an array comparative genomic hybridization profile that identifies triple-negative breast cancers (TNBC), with BRCA1 dysfunction and a high sensitivity to intensified dose bifunctional alkylating agents. To determine the effect of conventional-dose chemotherapy in patients with this so-called BRCA1-like profile, clinical characteristics and survival were studied in a large group of TNBC patients.

More about this publication

Annals of oncology : official journal of the European Society for Medical Oncology

Volume 23
Issue nr. 9
Pages 2301-2305
Publication date 01-09-2012

Full text links

Publisher website (DOI) 10.1093/annonc/mdr621
Europe PubMed Central 22357256
Pubmed 22357256

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