HER2 and response to paclitaxel in node-positive breast cancer

被引:421
|
作者
Hayes, Daniel F.
Thor, Ann D.
Dressler, Lynn G.
Weaver, Donald
Edgerton, Susan
Cowan, David
Broadwater, Gloria
Goldstein, Lori J.
Martino, Silvana
Ingle, James N.
Henderson, I. Craig
Norton, Larry
Winer, Eric P.
Hudis, Clifford A.
Ellis, Matthew J.
Berry, Donald A.
机构
[1] Univ Michigan, Canc Ctr 6312, Breast Oncol Program, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[2] Univ Colorado, Ctr Comprehens Canc, Aurora, CO USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[4] Univ Vermont, Ctr Canc, Fletcher Allen Hlth Care, Burlington, VT USA
[5] Duke Univ, Ctr Stat, Canc & Leukemia Grp B, Durham, NC USA
[6] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[7] Angeles Clin & Res Inst, Santa Monica, CA USA
[8] Mayo Clin, Rochester, MN USA
[9] Univ Calif San Francisco, San Francisco, CA 94143 USA
[10] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[11] Dana Farber Canc Inst, Boston, MA 02115 USA
[12] Washington Univ, Sch Med, Siteman Canc Ctr, St Louis, MO USA
[13] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2007年 / 357卷 / 15期
关键词
D O I
10.1056/NEJMoa071167
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The status of human epidermal growth factor receptor type 2 (HER2) in breast-cancer cells predicts clinical outcomes in women who receive adjuvant anthracycline-based chemotherapy. We hypothesized that HER2 positivity predicts a benefit from adjuvant doxorubicin doses above standard levels, from the addition of paclitaxel after adjuvant chemotherapy with doxorubicin plus cyclophosphamide, or from both. Methods We randomly selected 1500 women from 3121 women with node-positive breast cancer who had been randomly assigned to receive doxorubicin (60, 75, or 90 mg per square meter of body-surface area) plus cyclophosphamide (600 mg per square meter) for four cycles, followed by four cycles of paclitaxel (175 mg per square meter) or observation. Tissue blocks from 1322 of these 1500 women were available. Immunohistochemical analyses of these tissue specimens for HER2 with the CB11 monoclonal antibody against HER2 or with a polyclonal-antibody assay kit and fluorescence in situ hybridization for HER2 amplification were performed. Results No interaction was observed between HER2 positivity and doxorubicin doses above 60 mg per square meter. HER2 positivity was, however, associated with a significant benefit from paclitaxel. The interaction between HER2 positivity and the addition of paclitaxel to the treatment was associated with a hazard ratio for recurrence of 0.59 (P=0.01). Patients with a HER2-positive breast cancer benefited from paclitaxel, regardless of estrogen-receptor status, but paclitaxel did not benefit patients with HER2-negative, estrogen-receptor-positive cancers. Conclusions The expression or amplification, or both, of HER2 by a breast cancer is associated with a benefit from the addition of paclitaxel after adjuvant treatment with doxorubicin (<60 mg per square meter) plus cyclophosphamide in node-positive breast cancer, regardless of estrogen-receptor status. Patients with HER2-negative, estrogen-receptor-positive, node-positive breast cancer may gain little benefit from the administration of paclitaxel after adjuvant chemotherapy with doxorubicin plus cyclophosphamide.
引用
收藏
页码:1496 / 1506
页数:11
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