Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Ooe, Asakoa; * | Takahara, Sachikob | Sumiyoshi, Kazuhiroa | Yamamoto, Hitoshia | Kawai, Junc | Shiba, Eiichia
Affiliations: [a] Osaka Breast Clinic, Osaka, Japan | [b] Department of Breast Surgery, Kitano Hospital, Osaka, Japan | [c] Department of Pathology, Kansai Denryoku Hospital, Osaka, Japan
Correspondence: [*] Corresponding author: Asako Ooe, Osaka Breast Clinic, 1-3-4 Fukushima, Fukushima-ku, Osaka 553-0003, Japan. Tel.: +81 6 6450 4108; Fax: +81 6 6454 0041; E-mail: [email protected]
Abstract: Background:For locally advanced breast cancer, neoadjuvant chemotherapy (NAC) is the standard of care for downstaging the tumor prior to surgery, and improved prognoses that are associated with pathological complete responses (pCR) have been noted, particularly in patients with human epidermal growth factor receptor 2 (HER2)-positive and triple negative (TN) tumors. Objective:The aim of this study was to assess the differences in pathological responses among intrinsic subtypes of local lesions and status of axillary lymph nodes (Ax LN). Methods:A consecutive series of 134 patients with locally advanced breast cancer who were treated with NAC was analyzed. Tumors were classified into the following 5 subtypes according to immunohistochemical staining results: Luminal A type, Luminal B type (HER2-negative and HER2-positive), HER2 type, and TN type. Results:In Luminal A, Luminal B (HER2-negative), Luminal B (HER2-positive), HER2, and TN tumors, the pCR rates were 10% (4 of 40), 19% (8 of 42), 42% (8 of 19), 59% (10 of 17), and 38% (6 of 16), respectively. HER2-positive tumors showed good therapeutic effects, while Luminal A tumors showed less therapeutic effects. Conclusions:Strategies that are determined according to intrinsic subtypes are becoming very important in the treatment of locally advanced breast cancer.
Keywords: Intrinsic subtypes of breast cancer, neoadjuvant chemotherapy, therapeutic response
DOI: 10.3233/BD-130345
Journal: Breast Disease, vol. 34, no. 1, pp. 9-17, 2013
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]