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Pathologic complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients.
- Source :
-
Breast cancer research and treatment [Breast Cancer Res Treat] 2014 Sep; Vol. 147 (2), pp. 401-5. Date of Electronic Publication: 2014 Aug 17. - Publication Year :
- 2014
-
Abstract
- The aim of this study is to estimate the frequency of pathologic complete response (pCR) after neoadjuvant treatment with cisplatin chemotherapy in women with breast cancer and a BRCA1 mutation. One hundred and seven women with breast cancer and a BRCA1 mutation, who were diagnosed with stage I to III breast cancer between December 2006 and June 2014, were treated with cisplatin 75 mg/m(2) every 3 weeks for four cycles, followed by mastectomy and conventional chemotherapy. Information was collected on clinical stage, grade, hormone receptor status, and Her2neu status prior to treatment. pCR was determined by review of surgical specimens. One hundred and seven patients were enrolled in the study, including 93 patients who were treated for first primary breast cancer and 14 patients who had previously received treatment for a prior cancer. A pCR was observed in 65 of the 107 patients (61 %). Platinum-based chemotherapy is effective in a high proportion of patients with BRCA1-associated breast cancer.
- Subjects :
- Adult
Aged
BRCA1 Protein genetics
Breast Neoplasms metabolism
Breast Neoplasms surgery
Cisplatin administration & dosage
Cyclophosphamide administration & dosage
Doxorubicin administration & dosage
Female
Humans
Middle Aged
Neoadjuvant Therapy
Neoplasm Staging
Receptor, ErbB-2 administration & dosage
Young Adult
Antineoplastic Combined Chemotherapy Protocols therapeutic use
BRCA1 Protein biosynthesis
Breast Neoplasms drug therapy
Breast Neoplasms genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1573-7217
- Volume :
- 147
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Breast cancer research and treatment
- Publication Type :
- Academic Journal
- Accession number :
- 25129345
- Full Text :
- https://doi.org/10.1007/s10549-014-3100-x