Gene expression signatures, clinicopathological features, and individualized therapy in breast cancer.

@article{citeulike:2804739, abstract = {CONTEXT: Gene expression profiling may be useful for prognostic and therapeutic strategies in breast carcinoma. OBJECTIVES: To demonstrate the value in integrating genomic information with clinical and pathological risk factors, to refine prognosis, and to improve therapeutic strategies for early stage breast cancer. DESIGN, SETTING, AND PATIENTS: Retrospective study of patients with early stage breast carcinoma who were candidates for adjuvant chemotherapy; 964 clinically annotated breast tumor samples (573 in the initial discovery set and 391 in the validation cohort) with corresponding microarray data were used. All patients were assigned relapse risk scores based on their respective clinicopathological features. Signatures representing oncogenic pathway activation and tumor biology/microenvironment status were applied to these samples to obtain patterns of deregulation that correspond with relapse risk scores to refine prognosis with the clinicopathological prognostic model alone. Predictors of chemotherapeutic response were also applied to further characterize clinically relevant heterogeneity in early stage breast cancer. MAIN OUTCOME MEASURES: Gene expression signatures and clinicopathological variables in early stage breast cancer to determine a refined estimation of relapse-free survival and sensitivity to chemotherapy. RESULTS: In the initial data set of 573 patients, prognostically significant clusters representing patterns of oncogenic pathway activation and tumor biology/microenvironment states were identified within the low-risk (log-rank P = .004), intermediate-risk (log-rank P = .01), and high-risk (log-rank P = .003) model cohorts, representing clinically important genomic subphenotypes of breast cancer. As an example, in the low-risk cohort, of 6 prognostically significant clusters, patients in cluster 4 had an inferior relapse-free survival vs patients in cluster 1 (log-rank P = .004) and cluster 5 (log-rank P = .03). Median relapse-free survival for patients in cluster 4 was 16 months less than for patients in cluster 1 (95\% CI, 7.5-24.5 months) and 19 months less than for patients in cluster 5 (95\% CI, 10.5-27.5 months). Multivariate analyses confirmed the independent prognostic value of the genomic clusters (low risk, P = .05; high risk, P = .02). The reproducibility and validity of these patterns of pathway deregulation in predicting relapse risk was established using related but not identical clusters in the independent validation cohort. The prognostic clinicogenomic clusters also have unique sensitivity patterns to commonly used cytotoxic therapies. CONCLUSIONS: These results provide preliminary evidence that incorporation of gene expression signatures into clinical risk stratification can refine prognosis. Prospective studies are needed to determine the value of this approach for individualizing therapeutic strategies.}, address = {Duke Institute for Genome Sciences and Policy, Duke University, Durham, North Carolina 27708, USA.}, author = {Acharya, C. R. and Hsu, D. S. and Anders, C. K. and Anguiano, A. and Salter, K. H. and Walters, K. S. and Redman, R. C. and Tuchman, S. A. and Moylan, C. A. and Mukherjee, S. and Barry, W. T. and Dressman, H. K. and Ginsburg, G. S. and Marcom, K. P. and Garman, K. S. and Lyman, G. H. and Nevins, J. R. and Potti, A. }, citeulike-article-id = {2804739}, doi = {10.1001/jama.299.13.1574}, issn = {1538-3598}, journal = {JAMA : the journal of the American Medical Association}, keywords = {bio\_signature, breast\_cancer, classification, gene\_expression, therapy}, month = {April}, number = {13}, pages = {1574--1587}, posted-at = {2008-05-16 10:17:02}, priority = {0}, title = {Gene expression signatures, clinicopathological features, and individualized therapy in breast cancer.}, url = {http://dx.doi.org/10.1001/jama.299.13.1574}, volume = {299}, year = {2008} }

TY - JOUR ID - citeulike:2804739 L3 - citeulike-article-id:2804739 TI - Gene expression signatures, clinicopathological features, and individualized therapy in breast cancer. JF - JAMA : the journal of the American Medical Association VL - 299 IS - 13 SP - 1574 EP - 1587 AD - Duke Institute for Genome Sciences and Policy, Duke University, Durham, North Carolina 27708, USA. SN - 1538-3598 N2 - CONTEXT: Gene expression profiling may be useful for prognostic and therapeutic strategies in breast carcinoma. OBJECTIVES: To demonstrate the value in integrating genomic information with clinical and pathological risk factors, to refine prognosis, and to improve therapeutic strategies for early stage breast cancer. DESIGN, SETTING, AND PATIENTS: Retrospective study of patients with early stage breast carcinoma who were candidates for adjuvant chemotherapy; 964 clinically annotated breast tumor samples (573 in the initial discovery set and 391 in the validation cohort) with corresponding microarray data were used. All patients were assigned relapse risk scores based on their respective clinicopathological features. Signatures representing oncogenic pathway activation and tumor biology/microenvironment status were applied to these samples to obtain patterns of deregulation that correspond with relapse risk scores to refine prognosis with the clinicopathological prognostic model alone. Predictors of chemotherapeutic response were also applied to further characterize clinically relevant heterogeneity in early stage breast cancer. MAIN OUTCOME MEASURES: Gene expression signatures and clinicopathological variables in early stage breast cancer to determine a refined estimation of relapse-free survival and sensitivity to chemotherapy. RESULTS: In the initial data set of 573 patients, prognostically significant clusters representing patterns of oncogenic pathway activation and tumor biology/microenvironment states were identified within the low-risk (log-rank P = .004), intermediate-risk (log-rank P = .01), and high-risk (log-rank P = .003) model cohorts, representing clinically important genomic subphenotypes of breast cancer. As an example, in the low-risk cohort, of 6 prognostically significant clusters, patients in cluster 4 had an inferior relapse-free survival vs patients in cluster 1 (log-rank P = .004) and cluster 5 (log-rank P = .03). Median relapse-free survival for patients in cluster 4 was 16 months less than for patients in cluster 1 (95% CI, 7.5-24.5 months) and 19 months less than for patients in cluster 5 (95% CI, 10.5-27.5 months). Multivariate analyses confirmed the independent prognostic value of the genomic clusters (low risk, P = .05; high risk, P = .02). The reproducibility and validity of these patterns of pathway deregulation in predicting relapse risk was established using related but not identical clusters in the independent validation cohort. The prognostic clinicogenomic clusters also have unique sensitivity patterns to commonly used cytotoxic therapies. CONCLUSIONS: These results provide preliminary evidence that incorporation of gene expression signatures into clinical risk stratification can refine prognosis. Prospective studies are needed to determine the value of this approach for individualizing therapeutic strategies. KW - bio_signature KW - breast_cancer KW - classification KW - gene_expression KW - therapy AU - Acharya, CR AU - Hsu, DS AU - Anders, CK AU - Anguiano, A AU - Salter, KH AU - Walters, KS AU - Redman, RC AU - Tuchman, SA AU - Moylan, CA AU - Mukherjee, S AU - Barry, WT AU - Dressman, HK AU - Ginsburg, GS AU - Marcom, KP AU - Garman, KS AU - Lyman, GH AU - Nevins, JR AU - Potti, A PY - 2008/04/02/ UR - http://dx.doi.org/10.1001/jama.299.13.1574 ER -