A gene-expression signature to predict survival in breast cancer across independent data sets

被引:200
作者
Naderi, A.
Teschendorff, A. E.
Barbosa-Morais, N. I.
Pinder, S. E.
Green, A. R.
Powe, D. G.
Robertson, J. F. R.
Aparicio, S.
Ellis, I. O.
Brenton, J. D.
Caldas, C.
机构
[1] Univ Cambridge, Canc Genom Program, Dept Oncol, Hutchison Res Ctr,MRC, Cambridge CB2 2XZ, England
[2] Univ Cambridge, Dept Pathol, MRC, Hutchison Res Ctr, Cambridge CB2 2XZ, England
[3] Univ Nottingham, Nottingham NG7 2RD, England
[4] Nottingham City Hosp NHS Trust, Dept Mol Med Sci, Nottingham, England
[5] Nottingham City Hosp NHS Trust, Dept Med & Surg Sci, Nottingham, England
[6] Nottingham City Hosp NHS Trust, Dept Histopathol, Nottingham, England
[7] Univ Lisbon, Fac Med, Inst Mol Med, P-1699 Lisbon, Portugal
关键词
breast cancer; microarray; prognosis; gene-signature; survival; Cox-clustering;
D O I
10.1038/sj.onc.1209920
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prognostic signatures in breast cancer derived from microarray expression pro. ling have been reported by two independent groups. These signatures, however, have not been validated in external studies, making clinical application problematic. We performed microarray expression pro. ling of 135 early-stage tumors, from a cohort representative of the demographics of breast cancer. Using a recently proposed semisupervised method, we identified a prognostic signature of 70 genes that significantly correlated with survival ( hazard ratio (HR): 5.97, 95% confidence interval: 3.0-11.9, P = 2.7e-07). In multivariate analysis, the signature performed independently of other standard prognostic classifiers such as the Nottingham Prognostic Index and the 'Adjuvant!' software. Using two different prognostic classification schemes and measures, nearest centroid ( HR) and risk ordering (D-index), the 70-gene classifier was also found to be prognostic in two independent external data sets. Overall, the 70- gene set was prognostic in our study and the two external studies which collectively include 715 patients. In contrast, we found that the two previously described prognostic gene sets performed less optimally in external validation. Finally, a common prognostic module of 29 genes that associated with survival in both our cohort and the two external data sets was identified. In spite of these results, further studies that pro. le larger cohorts using a single microarray platform, will be needed before prospective clinical use of molecular classifiers can be contemplated.
引用
收藏
页码:1507 / 1516
页数:10
相关论文
共 25 条
[1]   Semi-supervised methods to predict patient survival from gene expression data [J].
Bair, E ;
Tibshirani, R .
PLOS BIOLOGY, 2004, 2 (04) :511-522
[2]   Molecular classification and molecular forecasting of breast cancer: Ready for clinical application? [J].
Brenton, JD ;
Carey, LA ;
Ahmed, AA ;
Caldas, C .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (29) :7350-7360
[3]   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
[4]  
Cox DR., 1984, ANAL SURVIVAL DATA
[5]   A cell proliferation signature is a marker of extremely poor outcome in a subpopulation of breast cancer patients [J].
Dai, HY ;
van't Veer, L ;
Lamb, J ;
He, YD ;
Mao, M ;
Fine, BM ;
Bernards, R ;
de Vijver, MV ;
Deutsch, P ;
Sachs, A ;
Stoughton, R ;
Friend, S .
CANCER RESEARCH, 2005, 65 (10) :4059-4066
[6]   Association of the breast cancer protein MLN51 with the Exon junction complex via its speckle localizer and RNA binding module [J].
Degot, S ;
Le Hir, H ;
Alpy, F ;
Kedinger, V ;
Stoll, I ;
Wendling, C ;
Seraphin, B ;
Rio, MC ;
Tomasetto, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) :33702-33715
[7]   Good Old clinical markers have similar power in breast cancer prognosis as microarray gene expression profilers [J].
Edén, P ;
Ritz, C ;
Rose, C ;
Fernö, M ;
Peterson, C .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (12) :1837-1841
[8]   Outcome signature genes in breast cancer: is there a unique set? [J].
Ein-Dor, L ;
Kela, I ;
Getz, G ;
Givol, D ;
Domany, E .
BIOINFORMATICS, 2005, 21 (02) :171-178
[9]   THE NOTTINGHAM PROGNOSTIC INDEX IN PRIMARY BREAST-CANCER [J].
GALEA, MH ;
BLAMEY, RW ;
ELSTON, CE ;
ELLIS, IO .
BREAST CANCER RESEARCH AND TREATMENT, 1992, 22 (03) :207-219
[10]   Multiple-laboratory comparison of microarray platforms [J].
Irizarry, RA ;
Warren, D ;
Spencer, F ;
Kim, IF ;
Biswal, S ;
Frank, BC ;
Gabrielson, E ;
Garcia, JGN ;
Geoghegan, J ;
Germino, G ;
Griffin, C ;
Hilmer, SC ;
Hoffman, E ;
Jedlicka, AE ;
Kawasaki, E ;
Martínez-Murillo, F ;
Morsberger, L ;
Lee, H ;
Petersen, D ;
Quackenbush, J ;
Scott, A ;
Wilson, M ;
Yang, YQ ;
Ye, SQ ;
Yu, W .
NATURE METHODS, 2005, 2 (05) :345-349