TY - JOUR
T1 - Validated prediction of clinical outcome in sarcomas and multiple types of cancer on the basis of a gene expression signature related to genome complexity
AU - Chibon, Frédéric
AU - Lagarde, Pauline
AU - Salas, Sébastien
AU - Pérot, Gaëlle
AU - Brouste, Véronique
AU - Tirode, Franck
AU - Lucchesi, Carlo
AU - De Reynies, Aurélien
AU - Kauffmann, Audrey
AU - Bui, Binh
AU - Terrier, Philippe
AU - Bonvalot, Sylvie
AU - Le Cesne, Axel
AU - Vince-Ranchère, Dominique
AU - Blay, Jean Yves
AU - Collin, Françoise
AU - Guillou, Louis
AU - Leroux, Agnès
AU - Coindre, Jean Michel
AU - Aurias, Alain
N1 - Funding Information:
This work was supported by grants from the French Institut National du Cancer, the French Projets Hospitaliers de Recherche Clinique program, the European Connective Tissue Cancer Network, the Curie Institute, the Bergonie Cancer Institute and l’INSERM. The construction of the human BAC array was supported by grants from the Carte d’Identité des Tumeurs program of the French Ligue Nationale Contre le Cancer. We are grateful to members of the French Sarcoma Group for providing tumor samples : Y.-M. Robin, X. Leroy, X. Saster-Garau, B. Marquès, M-C. Château, J-P. Ghnassia and F. Mishelany, J-B. Courrège, V. Dapremont and C. Ferreira. We would like to thank R. Maki and R. Iggo for critical reading of the manuscript. We thank R. Cook for English editing.
PY - 2010/1/1
Y1 - 2010/1/1
N2 - Sarcomas are heterogeneous and aggressive mesenchymal tumors. Histological grading has so far been the best predictor for metastasis-free survival, but it has several limitations, such as moderate reproducibility and poor prognostic value for some histological types. To improve patient grading, we performed genomic and expression profiling in a training set of 183 sarcomas and established a prognostic gene expression signature, complexity index in sarcomas (CINSARC), composed of 67 genes related to mitosis and chromosome management. In a multivariate analysis, CINSARC predicts metastasis outcome in the training set and in an independent 127 sarcomas validation set. It is superior to the Fédération Francaise des Centres de Lutte Contre le Cancer grading system in determining metastatic outcome for sarcoma patients. Furthermore, it also predicts outcome for gastrointestinal stromal tumors (GISTs), breast carcinomas and lymphomas. Application of the signature will permit more selective use of adjuvant therapies for people with sarcomas, leading to decreased iatrogenic morbidity and improved outcomes for such individuals.
AB - Sarcomas are heterogeneous and aggressive mesenchymal tumors. Histological grading has so far been the best predictor for metastasis-free survival, but it has several limitations, such as moderate reproducibility and poor prognostic value for some histological types. To improve patient grading, we performed genomic and expression profiling in a training set of 183 sarcomas and established a prognostic gene expression signature, complexity index in sarcomas (CINSARC), composed of 67 genes related to mitosis and chromosome management. In a multivariate analysis, CINSARC predicts metastasis outcome in the training set and in an independent 127 sarcomas validation set. It is superior to the Fédération Francaise des Centres de Lutte Contre le Cancer grading system in determining metastatic outcome for sarcoma patients. Furthermore, it also predicts outcome for gastrointestinal stromal tumors (GISTs), breast carcinomas and lymphomas. Application of the signature will permit more selective use of adjuvant therapies for people with sarcomas, leading to decreased iatrogenic morbidity and improved outcomes for such individuals.
UR - http://www.scopus.com/inward/record.url?scp=77954535843&partnerID=8YFLogxK
U2 - 10.1038/nm.2174
DO - 10.1038/nm.2174
M3 - Article
AN - SCOPUS:77954535843
SN - 1078-8956
VL - 16
SP - 781
EP - 787
JO - Nature Medicine
JF - Nature Medicine
IS - 7
ER -