A Multigene Expression Assay to Predict Local Recurrence Risk for Ductal Carcinoma In Situ of the Breast

被引:403
作者
Solin, Lawrence J. [1 ]
Gray, Robert [2 ,3 ]
Baehner, Frederick L. [4 ,5 ]
Butler, Steven M. [4 ]
Hughes, Lorie L. [6 ]
Yoshizawa, Carl [4 ]
Cherbavaz, Diana B. [4 ]
Shak, Steven [4 ]
Page, David L. [7 ]
Sledge, George W., Jr. [8 ]
Davidson, Nancy E. [10 ]
Ingle, James N. [11 ]
Perez, Edith A. [12 ]
Wood, William C. [13 ]
Sparano, Joseph A. [14 ]
Badve, Sunil [9 ]
机构
[1] Albert Einstein Med Ctr, Dept Radiat Oncol, Philadelphia, PA 19141 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Eastern Cooperat Oncol Grp Coordinating Ctr, Boston, MA USA
[4] Genom Hlth Inc, Redwood City, CA USA
[5] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
[6] City Hope Natl Med Ctr, Cartersville, GA USA
[7] Vanderbilt Univ, Dept Pathol, Nashville, TN USA
[8] Indiana Univ, Dept Med Oncol, Indianapolis, IN 46204 USA
[9] Indiana Univ, Dept Pathol, Indianapolis, IN 46204 USA
[10] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
[11] Mayo Clin, Rochester, MN USA
[12] Mayo Clin, Jacksonville, FL 32224 USA
[13] Emory Univ, Dept Surg, Atlanta, GA 30322 USA
[14] Albert Einstein Coll Med, Dept Med Oncol, Montefiore Med Ctr, New York, NY USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2013年 / 105卷 / 10期
基金
美国国家卫生研究院;
关键词
SURGICAL ADJUVANT BREAST; GENE-EXPRESSION; EUROPEAN ORGANIZATION; CONSERVING THERAPY; CANCER; TAMOXIFEN; RADIOTHERAPY; RADIATION; PROTOCOL; SURGERY;
D O I
10.1093/jnci/djt067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background For women with ductal carcinoma in situ (DCIS) of the breast, the risk of developing an ipsilateral breast event (IBE; defined as local recurrence of DCIS or invasive carcinoma) after surgical excision without radiation is not well defined by clinical and pathologic characteristics. Methods The Oncotype DX breast cancer assay was performed for patients with DCIS treated with surgical excision without radiation in the Eastern Cooperative Oncology Group (ECOG) E5194 study. The association of the prospectively defined DCIS Score (calculated from seven cancer-related genes and five reference genes) with the risk of developing an IBE was analyzed using Cox regression. All statistical tests were two-sided. Results There were 327 patients with adequate tissue for analysis. The continuous DCIS Score was statistically significantly associated with the risk of developing an IBE (hazard ratio [HR] = 2.31, 95% confidence interval [CI] = 1.15 to 4.49; P = .02) when adjusted for tamoxifen use (prespecified primary analysis) and with invasive IBE (unadjusted HR = 3.68, 95% CI = 1.34 to 9.62; P = .01). For the prespecified DCIS risk groups of low, intermediate, and high, the 10-year risks of developing an IBE were 10.6%, 26.7%, and 25.9%, respectively, and for an invasive IBE, 3.7%, 12.3%, and 19.2%, respectively (both log rank P = .006). In multivariable analyses, factors associated with IBE risk were DCIS Score, tumor size, and menopausal status (all P = .02). Conclusions The DCIS Score quantifies IBE risk and invasive IBE risk, complements traditional clinical and pathologic factors, and provides a new clinical tool to improve selecting individualized treatment for women with DCIS who meet the ECOG E5194 criteria.
引用
收藏
页码:701 / 710
页数:10
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