Prognostic utility of the 21-gene assay in hormone receptor-positive operable breast cancer compared with classical clinicopathologic features

被引:252
作者
Goldstein, Lori J.
Gray, Robert
Badve, Sunil
Childs, Barrett H.
Yoshizawa, Carl
Rowley, Steve
Shak, Steven
Baehner, Frederick L.
Ravdin, Peter M.
Davidson, Nancy E.
Sledge, George W., Jr.
Perez, Edith A.
Shulman, Lawrence N.
Martino, Silvana
Sparano, Joseph A.
机构
[1] Eastern Cooperat Oncol Grp, Boston, MA USA
[2] Sanofi Aventis, Bridgewater, NJ USA
[3] Genom Hlth Inc, Redwood City, CA USA
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[5] SW Oncol Grp, San Antonio, TX USA
[6] N Cent Canc Treatment Grp, Rochester, MN USA
[7] Canc & Leukemia Grp B, Chicago, IL USA
基金
美国国家卫生研究院;
关键词
D O I
10.1200/JCO.2007.14.4501
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Adjuvant! is a standardized validated decision aid that projects outcomes in operable breast cancer based on classical clinicopathologic features and therapy. Genomic classifiers offer the potential to more accurately identify individuals who benefit from chemotherapy than clinicopathologic features. Patients and Methods A sample of 465 patients with hormone receptor (HR) -positive breast cancer with zero to three positive axillary nodes who did (n = 99) or did not have recurrence after chemohormonal therapy had tumor tissue evaluated using a 21-gene assay. Histologic grade and HR expression were evaluated locally and in a central laboratory. Results Recurrence Score (RS) was a highly significant predictor of recurrence, including node-negative and node-positive disease (P <.001 for both) and when adjusted for other clinical variables. RS also predicted recurrence more accurately than clinical variables when integrated by an algorithm modeled after Adjuvant! that was adjusted to 5-year outcomes. The 5-year recurrence rate was only 5% or less for the estimated 46% of patients who have a low RS (<18). Conclusion The 21-gene assay was a more accurate predictor of relapse than standard clinical features for individual patients with HR-positive operable breast cancer treated with chemohormonal therapy and provides information that is complementary to features typically used in anatomic staging, such as tumor size and lymph node involvement. The 21-gene assay may be used to select low-risk patients for abbreviated chemotherapy regimens similar to those used in our study or high-risk patients for more aggressive regimens or clinical trials evaluating novel treatments.
引用
收藏
页码:4063 / 4071
页数:9
相关论文
共 32 条
[1]  
Abe O, 2005, LANCET, V365, P1687, DOI 10.1016/s0140-6736(05)66544-0
[2]  
Albain K, 2007, BREAST CANC RES T S1, V106
[3]  
Baum M., 2003, CANCER, V98, P1802, DOI DOI 10.1002/CNCR.11745
[4]   Estrogen-receptor status and outcomes of modern chemotherapy for patients with node-positive breast cancer [J].
Berry, DA ;
Cirrincione, C ;
Henderson, IC ;
Citron, ML ;
Budman, DR ;
Goldstein, LJ ;
Martino, S ;
Perez, EA ;
Muss, HB ;
Norton, L ;
Hudis, C ;
Winer, EP .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (14) :1658-1667
[5]   Effect of screening and adjuvant therapy on mortality from breast cancer [J].
Berry, DA ;
Cronin, KA ;
Plevritis, SK ;
Fryback, DG ;
Clarke, L ;
Zelen, M ;
Mandelblatt, JS ;
Yakovlev, AY ;
Habbema, JDF ;
Feuer, EJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1784-1792
[6]  
Carlson Robert W, 2006, J Natl Compr Canc Netw, V4 Suppl 3, pS1
[7]   Robustness, scalability, and integration of a wound-response gene expression signature in predicting breast cancer survival [J].
Chang, HY ;
Nuyten, DSA ;
Sneddon, JB ;
Hastie, T ;
Tibshirani, R ;
Sorlie, T ;
Dai, HY ;
He, YDD ;
van't Veer, LJ ;
Bartelink, H ;
van de Rijn, M ;
Brown, PO ;
van de Vijver, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3738-3743
[8]  
DALTON LW, 1994, CANCER, V73, P2765, DOI 10.1002/1097-0142(19940601)73:11<2765::AID-CNCR2820731119>3.0.CO
[9]  
2-K
[10]   Multicenter validation of a gene expression-based prognostic signature in lymph node-negative primary breast cancer [J].
Foekens, JA ;
Atkins, D ;
Zhang, Y ;
Sweep, FCGJ ;
Harbeck, N ;
Paradiso, A ;
Cufer, T ;
Sieuwerts, AM ;
Talantov, D ;
Span, PN ;
Tjan-Heijnen, VCG ;
Zito, AF ;
Specht, K ;
Hoefler, H ;
Golouh, R ;
Schittulli, F ;
Schmitt, M ;
Beex, LVAM ;
Klijn, IGM ;
Wang, YX .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (11) :1665-1671