Pathologic Complete Response Rates in Young Women With BRCA1-Positive Breast Cancers After Neoadjuvant Chemotherapy

被引:421
作者
Byrski, Tomasz
Gronwald, Jacek
Huzarski, Tomasz
Grzybowska, Ewa
Budryk, Magdalena
Stawicka, Malgorzata
Mierzwa, Tomasz
Szwiec, Marek
Wisniowski, Rafal
Siolek, Monika
Dent, Rebecca
Lubinski, Jan
Narod, Steven [1 ]
机构
[1] Univ Toronto, Res Inst, Womens Coll, Toronto, ON M5G 1NB, Canada
关键词
OVARIAN-CANCER; BRCA1; MUTATIONS; GENE; PHENOTYPE; FEATURES; SUBTYPES;
D O I
10.1200/JCO.2008.20.7019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To estimate the rate of pathologic complete response (pCR) to neoadjuvant chemotherapy in BRCA1 mutation carriers according to chemotherapy regimen. Patients and Methods From a registry of 6,903 patients, we identified 102 women who carried a BRCA1 founder mutation and who had been treated for breast cancer with neoadjuvant chemotherapy. Pathologic complete response was evaluated using standard criteria. Results Twenty-four (24%) of the 102 BRCA1 mutation carriers experienced a pCR. The response rate varied widely with treatment: a pCR was observed in one (7%) of 14 women treated with cyclophosphamide, methotrexate, and fluorouracil (CMF); in two (8%) of 25 women treated with doxorubicin and docetaxel (AT); in 11 (22%) of 51 women treated with doxorubicin and cyclophosphamide (AC) or fluorouracil, doxorubicin, and cyclophosphamide (FAC), and in 10 (83%) of 12 women treated with cisplatin. Conclusion A low rate of pCR was observed in women with breast cancer and a BRCA1 mutation who were treated with AT or CMF. A high rate of pCR was seen after treatment with cisplatin. An intermediate rate of PCR was associated with AC or FAC. The relative benefits of AC and platinum therapy need to be confirmed through follow-up of this and other cohorts.
引用
收藏
页码:375 / 379
页数:5
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