Strong time dependence of the 76-gene prognostic signature for node-negative breast cancer patients in the TRANSBIG multicenter independent validation series

被引:727
作者
Desmedt, Christine
Piette, Fanny
Loi, Sherene
Wang, Yixin
d'assignies, Mahasti Saghatchian
Bergh, Jonas
Lidereau, Rosette
Ellis, Paul
Harris, Adrian L.
Klijn, Jan G. M.
Foekens, John A.
Cardoso, Fatima
Piccart, Martine J.
Buyse, Marc
Sotiriou, Christos
机构
[1] Univ Libre Bruxelles, Inst Jules Bordet, TRANSBIG Secretariat, Breast Int Grp, B-1000 Brussels, Belgium
[2] Univ Libre Bruxelles, Int Inst Drug Dev, B-1000 Brussels, Belgium
[3] Univ Libre Bruxelles, Machine Learning Grp, B-1000 Brussels, Belgium
[4] Veridex LLC, San Diego, CA USA
[5] European Inst Oncol, Milan, Italy
[6] Univ Milan, Sch Med, Milan, Italy
[7] Swiss Inst Expt Canc Res, Natl Ctr Competence Res Mol Oncol, CH-1066 Epalinges, Switzerland
[8] Swiss Inst Bioinformat, Lausanne, Switzerland
[9] Inst Gustave Roussy, Villejuif, France
[10] Karolinska Inst, Stockholm, Sweden
[11] Ctr Rene Huguenin, St Cloud, France
[12] INSERM, St Cloud, France
[13] Guys Hosp, London SE1 9RT, England
[14] John Radcliffe Hosp, Oxford OX3 9DU, England
[15] Erasmus MC, Dr Daniel Denhoed Canc Ctr, Rotterdam, Netherlands
关键词
DISTANT METASTATIC SITES; ADJUVANT THERAPY; HER-2; STATUS; CONSENSUS; CELLS; WOMEN;
D O I
10.1158/1078-0432.CCR-06-2765
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Recently, a 76-gene prognostic signature able to predict distant metastases in lymph node - negative (N) breast cancer patients was reported. The aims of this study conducted by TRANSBIG were to independently validate these results and to compare the outcome with clinical risk assessment. Experimental Design: Gene expression profiling of frozen samples from 198 N- systemically untreated patients was done at the Bordet Institute, blinded to clinical data and independent of Veridex. Genomic risk was defined by Veridex, blinded to clinical data. Survival analyses, done by an independent statistician, were done with the genomic risk and adjusted for the clinical risk, defined by Adjuvant! Online. Results: The actual 5- and 10-year time to distant metastasis were 98% (88-100%) and 94% (83-98%), respectively, for the good profile group and 76% (68-82%) and 73% (65-79%), respectively, for the poor profile group. The actual 5- and 10-year overall survival were 98% (88-100%) and 87% (73-94%), respectively, for the good profile group and 84% (77-89%) and 72% (63-78%), respectively, for the poor profile group. We observed a strong time dependence of this signature, leading to an adjusted hazard ratio of 13.58 (1.85-99.63) and 8.20 (1.10-60.90) at 5 years and 5.11 (1.57-16.67) and 2.55 (1.07-6.10) at 10 years for time to distant metastasis and overall survival, respectively. Conclusion: This independent validation confirmed the performance of the 76-gene signature and adds to the growing evidence that gene expression signatures are of clinical relevance, especially for identifying patients at high risk of early distant metastases.
引用
收藏
页码:3207 / 3214
页数:8
相关论文
共 18 条
[1]   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
[2]  
DESMEDT C, 2006, 5 EUR BREAST CANC C
[3]   Comparison of topoisomerase-IIα gene status between primary breast cancer and corresponding distant metastatic sites [J].
Durbecq, V ;
Di Leo, A ;
Cardoso, F ;
Rouas, G ;
Leroy, JY ;
Piccart, M ;
Larsimont, D .
BREAST CANCER RESEARCH AND TREATMENT, 2003, 77 (03) :199-204
[4]  
Eifel P, 2001, JNCI-J NATL CANCER I, V93, P979
[5]   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
[6]   Comparison of HER-2 status between primary breast cancer and corresponding distant metastatic sites [J].
Gancberg, D ;
Di Leo, A ;
Cardoso, F ;
Rouas, G ;
Pedrocchi, M ;
Paesmans, M ;
Verhest, A ;
Bernard-Marty, C ;
Piccart, MJ ;
Larsimont, D .
ANNALS OF ONCOLOGY, 2002, 13 (07) :1036-1043
[7]   Meeting highlights:: Updated international expert consensus on the primary therapy of early breast cancer [J].
Goldhirsch, A ;
Wood, WC ;
Gelber, RD ;
Coates, AS ;
Thürlimann, B ;
Senn, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (17) :3357-3365
[8]   Comparison of HER-2 status determined by fluorescence in situ hybridization in primary and metastatic breast carcinoma [J].
Gong, Y ;
Booser, DJ ;
Sneige, N .
CANCER, 2005, 103 (09) :1763-1769
[9]   Genetic heterogeneity of single disseminated tumour cells in minimal residual cancer [J].
Klein, CA ;
Blankenstein, TJF ;
Schmidt-Kittler, O ;
Petronio, M ;
Polzer, B ;
Stoecklein, NH ;
Riethmüller, G .
LANCET, 2002, 360 (9334) :683-689
[10]   Prediction of cancer outcome with microarrays - Reply [J].
Klijn, JGM ;
Wang, YX ;
Atkins, D ;
Foekens, JA .
LANCET, 2005, 365 (9472) :1686-1686