Predicting a local recurrence after breast-conserving therapy by gene expression profiling

被引:153
作者
Nuyten, Dimitry S. A.
Kreike, Bas
Hart, Augustinus A. M.
Chi, Jen-Tsan Ashley
Sneddon, Julie B.
Wessels, Lodewyk F. A.
Peterse, Hans J.
Bartelink, Harry
Brown, Patrick O.
Chang, Howard Y.
van de Vijver, Marc J.
机构
[1] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Diagnost Oncol, NL-1066 CX Amsterdam, Netherlands
[2] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Radiat Oncol, NL-1066 CX Amsterdam, Netherlands
[3] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Expt Therapy, NL-1066 CX Amsterdam, Netherlands
[4] Stanford Univ, Dept Biochem, Sch Med, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Biochem, Howard Hughes Med Inst, Program Epithelial Biol, Stanford, CA 94305 USA
来源
BREAST CANCER RESEARCH | 2006年 / 8卷 / 05期
关键词
D O I
10.1186/bcr1614
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction To tailor local treatment in breast cancer patients there is a need for predicting ipsilateral recurrences after breast-conserving therapy. After adequate treatment ( excision with free margins and radiotherapy), young age and incompletely excised extensive intraductal component are predictors for local recurrence, but many local recurrences can still not be predicted. Here we have used gene expression profiling by microarray analysis to identify gene expression profiles that can help to predict local recurrence in individual patients. Methods By using previously established gene expression profiles with proven value in predicting metastasis- free and overall survival ( wound- response signature, 70- gene prognosis profile and hypoxia- induced profile) and training towards an optimal prediction of local recurrences in a training series, we establish a classifier for local recurrence after breast- conserving therapy. Results Validation of the different gene lists shows that the wound- response signature is able to separate patients with a high ( 29%) or low ( 5%) risk of a local recurrence at 10 years ( sensitivity 87.5%, specificity 75%). In multivariable analysis the classifier is an independent predictor for local recurrence. Conclusion Our findings indicate that gene expression profiling can identify subgroups of patients at increased risk of developing a local recurrence after breast- conserving therapy.
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页数:11
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共 39 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]   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
[3]   Recurrence rates after treatment of breast cancer with standard radiotherapy with or without additional radiation. [J].
Bartelink, H ;
Horiot, J ;
Poortmans, P ;
Struikmans, H ;
Van den Bogaert, W ;
Barillot, I ;
Fourquet, A ;
Borger, J ;
Jager, J ;
Hoogenraad, W ;
Collette, L ;
Pierart, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (19) :1378-1387
[4]  
Blichert-Toft M, 1992, J Natl Cancer Inst Monogr, P19
[5]   RISK-FACTORS IN BREAST-CONSERVATION THERAPY [J].
BORGER, J ;
KEMPERMAN, H ;
HART, A ;
PETERSE, H ;
VANDONGEN, J ;
BARTELINK, H .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (04) :653-660
[6]   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
[7]   Gene expression signature of fibroblast serum response predicts human cancer progression: Similarities between tumors and wounds [J].
Chang, HY ;
Sneddon, JB ;
Alizadeh, AA ;
Sood, R ;
West, RB ;
Montgomery, K ;
Chi, JT ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PLOS BIOLOGY, 2004, 2 (02) :206-214
[8]   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
[9]   Gene expression programs in response to hypoxia: Cell type specificity and prognostic significance in human cancers [J].
Chi, JT ;
Wang, Z ;
Nuyten, DSA ;
Rodriguez, EH ;
Schaner, ME ;
Salim, A ;
Wang, Y ;
Kristensen, GB ;
Helland, A ;
Borresen-Dale, AL ;
Giaccia, A ;
Longaker, MT ;
Hastie, T ;
Yang, GP ;
van de Vijver, MJ ;
Brown, PO .
PLOS MEDICINE, 2006, 3 (03) :395-409
[10]   Risk factors for local recurrence after breast-conserving therapy for invasive carcinomas: A case-control study of histological factors and alterations in oncogene expression [J].
Elkhuizen, PHM ;
Voogd, AC ;
van den Broek, LCJM ;
Tan, ITC ;
van Houwelingen, HC ;
Leer, JWH ;
van de Vijver, MJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 45 (01) :73-83