The predictive value of the 70-gene signature for adjuvant chemotherapy in early breast cancer

被引:180
作者
Knauer, Michael [1 ,2 ]
Mook, Stella [1 ]
Rutgers, Emiel J. T. [1 ]
Bender, Richard A. [3 ]
Hauptmann, Michael [1 ]
van de Vijver, Marc J. [1 ]
Koornstra, Rutger H. T. [1 ]
Bueno-de-Mesquita, Jolien M. [1 ]
Linn, Sabine C. [1 ]
van't Veer, Laura J. [1 ,4 ]
机构
[1] Netherlands Canc Inst, Div Diagnost Oncol, NL-1066 CX Amsterdam, Netherlands
[2] Acad Teaching Hosp Feldkirch, Dept Gen & Thorac Surg, A-6800 Feldkirch, Austria
[3] Agendia Inc, Huntington Beach, CA USA
[4] Agendia BV, Amsterdam, Netherlands
关键词
Breast cancer; Gene expression profiling; Adjuvant chemotherapy; Risk assessment; GENE-EXPRESSION PROFILES; PATHOLOGICAL RESPONSE; PROGNOSIS-SIGNATURE; GRADE INDEX; DOXORUBICIN; VALIDATION; DOCETAXEL; WOMEN; CYCLOPHOSPHAMIDE; FLUOROURACIL;
D O I
10.1007/s10549-010-0814-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multigene assays have been developed and validated to determine the prognosis of breast cancer. In this study, we assessed the additional predictive value of the 70-gene MammaPrint signature for chemotherapy (CT) benefit in addition to endocrine therapy (ET) from pooled study series. For 541 patients who received either ET (n = 315) or ET + CT (n = 226), breast cancer-specific survival (BCSS) and distant disease-free survival (DDFS) at 5 years were assessed separately for the 70-gene high and low risk groups. The 70-gene signature classified 252 patients (47%) as low risk and 289 (53%) as high risk. Within the 70-gene low risk group, BCSS was 97% for the ET group and 99% for the ET + CT group at 5 years with a non-significant univariate hazard ratio (HR) of 0.58 (95% CI 0.07-4.98; P = 0.62). In the 70-gene high risk group, BCSS was 81% (ET group) and 94% (ET + CT group) at 5 years with a significant HR of 0.21 (95% CI 0.07-0.59; P < 0.01). DDFS was 93% (ET) versus 99% (ET + CT), respectively, in the 70-gene low risk group, HR 0.26 (95% CI 0.03-2.02; P = 0.20). In the high risk group DDFS was 76 versus 88%, HR of 0.35 (95% CI 0.17-0.71; P < 0.01). Results were similar in multivariate analysis, showing significant survival benefit by adding CT in the 70-gene high risk group. A significant and clinically meaningful benefit was observed by adding chemotherapy to endocrine treatment in 70-gene high risk patients. This benefit was not significant in low risk patients, who were at such low risk for recurrence and cancer-related death, that adding CT does not appear to be clinically meaningful.
引用
收藏
页码:655 / 661
页数:7
相关论文
共 38 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]   Prognostic and predictive value of the 21-gene recurrence score assay in postmenopausal women with node-positive, oestrogen-receptor-positive breast cancer on chemotherapy: a retrospective analysis of a randomised trial [J].
Albain, Kathy S. ;
Barlow, William E. ;
Shak, Steven ;
Hortobagyi, Gabriel N. ;
Livingston, Robert B. ;
Yeh, I-Tien ;
Ravdin, Peter ;
Bugarini, Roberto ;
Boehner, Frederick L. ;
Davidson, Nancy E. ;
Sledge, George W. ;
Winer, Eric P. ;
Hudis, Clifford ;
Ingle, James N. ;
Perez, Edith A. ;
Pritchard, Kathleen I. ;
Shepherd, Lois ;
Gralow, Julie R. ;
Yoshizawa, Carl ;
Allred, D. Craig ;
Osborne, C. Kent ;
Hayes, Daniel F. .
LANCET ONCOLOGY, 2010, 11 (01) :55-65
[3]   Use of 70-gene signature to predict prognosis of patients with node-negative breast cancer: a prospective community-based feasibility study (RASTER) [J].
不详 .
LANCET ONCOLOGY, 2007, 8 (12) :1079-1087
[4]   Gene expression profiles predict complete pathologic response to neoadjuvant paclitaxel and fluorouracil, doxorubicin, and cyclophosphamide chemotherapy in breast cancer [J].
Ayers, M ;
Symmans, WF ;
Stec, J ;
Damokosh, AI ;
Clark, E ;
Hess, K ;
Lecocke, M ;
Metivier, J ;
Booser, D ;
Ibrahim, N ;
Valero, V ;
Royce, M ;
Arun, B ;
Whitman, G ;
Ross, J ;
Sneige, N ;
Hortobagyi, GN ;
Pusztai, L .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (12) :2284-2293
[6]   Validation of 70-gene prognosis signature in node-negative breast cancer [J].
Bueno-de-Mesquita, J. M. ;
Linn, S. C. ;
Keijzer, R. ;
Wesseling, J. ;
Nuyten, D. S. A. ;
van Krimpen, C. ;
Meijers, C. ;
de Graaf, P. W. ;
Bos, M. M. E. M. ;
Hart, A. A. M. ;
Rutgers, E. J. T. ;
Peterse, J. L. ;
Halfwerk, H. ;
de Groot, R. ;
Pronk, A. ;
Floore, A. N. ;
Glas, A. M. ;
van't Veer, L. J. ;
van de Vijver, M. J. .
BREAST CANCER RESEARCH AND TREATMENT, 2009, 117 (03) :483-495
[7]   Validation and clinical utility of a 70-gene prognostic signature for women with node-negative breast cancer [J].
Buyse, Marc ;
Loi, Sherene ;
van't Veer, Laura ;
Viale, Giuseppe ;
Delorenzi, Mauro ;
Glas, Annuska M. ;
d'Assignies, Mahasti Saghatchian ;
Bergh, Jonas ;
Lidereau, Rosette ;
Ellis, Paul ;
Harris, Adrian ;
Bogaerts, Jan ;
Therasse, Patrick ;
Floore, Arno ;
Amakrane, Mohamed ;
Piette, Fanny ;
Rutgers, Emiel ;
Sotiriou, Christos ;
Cardoso, Fatima ;
Piccart, Martine J. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (17) :1183-1192
[8]   Clinical application of the 70-gene profile: The MINDACT trial [J].
Cardoso, Fatima ;
Van't Veer, Laura ;
Rutgers, Emiel ;
Loi, Sherene ;
Mook, Stella ;
Piccart-Gebhart, Martine J. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (05) :729-735
[9]   Gene expression profiling for the prediction of therapeutic response to docetaxel in patients with breast cancer [J].
Chang, JC ;
Wooten, EC ;
Tsimelzon, A ;
Hilsenbeck, SG ;
Gutierrez, MC ;
Elledge, R ;
Mohsin, S ;
Osborne, CK ;
Chamness, GC ;
Allred, DC ;
O'Connell, P .
LANCET, 2003, 362 (9381) :362-369
[10]   International Web-based consultation on priorities for translational breast cancer research [J].
Dowsett, Mitch ;
Goldhirsch, Aron ;
Hayes, Daniel F. ;
Senn, Hans-Joerg ;
Wood, William ;
Viale, Giuseppe .
BREAST CANCER RESEARCH, 2007, 9 (06)