Association between the 21-gene recurrence score assay and risk of locoregional recurrence in node-negative, estrogen receptor-positive breast cancer: results from NSABP B-14 and NSABP B-20
- PMID: 20065188
- PMCID: PMC2849763
- DOI: 10.1200/JCO.2009.23.7610
Association between the 21-gene recurrence score assay and risk of locoregional recurrence in node-negative, estrogen receptor-positive breast cancer: results from NSABP B-14 and NSABP B-20
Abstract
Purpose: The 21-gene OncotypeDX recurrence score (RS) assay quantifies the risk of distant recurrence in tamoxifen-treated patients with node-negative, estrogen receptor (ER)-positive breast cancer. We investigated the association between RS and risk for locoregional recurrence (LRR) in patients with node-negative, ER-positive breast cancer from two National Surgical Adjuvant Breast and Bowel Project (NSABP) trials (NSABP B-14 and B-20).
Patients and methods: RS was available for 895 tamoxifen-treated patients (from both trials), 355 placebo-treated patients (from B-14), and 424 chemotherapy plus tamoxifen-treated patients (from B-20). The primary end point was time to first LRR. Distant metastases, second primary cancers, and deaths before LRR were censored.
Results: In tamoxifen-treated patients, LRR was significantly associated with RS risk groups (P < .001). The 10-year Kaplan-Meier estimate of LRR was 4.% (95% CI, 2.3% to 6.3%) for patients with a low RS (< 18), 7.2% (95% CI, 3.4% to 11.0%) for those with intermediate RS (18-30), and 15.8% (95% CI, 10.4% to 21.2%) for those with a high RS (> 30). There were also significant associations between RS and LRR in placebo-treated patients from B-14 (P = .022) and in chemotherapy plus tamoxifen-treated patients from B-20 (P = .028). In multivariate analysis, RS was an independent significant predictor of LRR along with age and type of initial treatment.
Conclusion: Similar to the association between RS and risk for distant recurrence, a significant association exists between RS and risk for LRR. This information has biologic consequences and potential clinical implications relative to locoregional therapy decisions for patients with node-negative and ER-positive breast cancer.
Conflict of interest statement
Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.
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Comment in
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Defining the clinical utility of gene expression assays in breast cancer: the intersection of science and art in clinical decision making.J Clin Oncol. 2010 Apr 1;28(10):1625-7. doi: 10.1200/JCO.2009.25.2882. Epub 2010 Jan 11. J Clin Oncol. 2010. PMID: 20065178 No abstract available.
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Molecular predictors of locoregional recurrence in breast cancer: ready for prime time?J Clin Oncol. 2010 Apr 1;28(10):1627-9. doi: 10.1200/JCO.2009.27.1080. Epub 2010 Mar 1. J Clin Oncol. 2010. PMID: 20194835 No abstract available.
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Risk factors. Oncotype DX assay predicts local recurrence in breast cancer.Nat Rev Clin Oncol. 2010 Jun;7(6):300. doi: 10.1038/nrclinonc.2010.75. Nat Rev Clin Oncol. 2010. PMID: 20527688 No abstract available.
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