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  • Prognostic and predictive v...
    Albain, Kathy S, Prof; Barlow, William E, Prof; Shak, Steven, MD; Hortobagyi, Gabriel N, Prof; Livingston, Robert B, Prof; Yeh, I-Tien, Prof; Ravdin, Peter, Prof; Bugarini, Roberto, DStat; Baehner, Frederick L, MD; Davidson, Nancy E, Prof; Sledge, George W, Prof; Winer, Eric P, Prof; Hudis, Clifford, Prof; Ingle, James N, Prof; Perez, Edith A, Prof; Pritchard, Kathleen I, Prof; Shepherd, Lois, Prof; Gralow, Julie R, Prof; Yoshizawa, Carl, PhD; Allred, D Craig, Prof; Osborne, C Kent, Prof; Hayes, Daniel F, Prof

    The lancet oncology, 2010, 2010-Jan, 2010-01-00, 20100101, Letnik: 11, Številka: 1
    Journal Article

    Summary Background The 21-gene recurrence score assay is prognostic for women with node-negative, oestrogen-receptor-positive breast cancer treated with tamoxifen. A low recurrence score predicts little benefit of chemotherapy. For node-positive breast cancer, we investigated whether the recurrence score was prognostic in women treated with tamoxifen alone and whether it identified those who might not benefit from anthracycline-based chemotherapy, despite higher risks of recurrence. Methods The phase 3 trial SWOG-8814 for postmenopausal women with node-positive, oestrogen-receptor-positive breast cancer showed that chemotherapy with cyclophosphamide, doxorubicin, and fluorouracil (CAF) before tamoxifen (CAF-T) added survival benefit to treatment with tamoxifen alone. Optional tumour banking yielded specimens for determination of recurrence score by RT-PCR. In this retrospective analysis, we assessed the effect of recurrence score on disease-free survival by treatment group (tamoxifen vs CAF-T) using Cox regression, adjusting for number of positive nodes. Findings There were 367 specimens (40% of the 927 patients in the tamoxifen and CAF-T groups) with sufficient RNA for analysis (tamoxifen, n=148; CAF-T, n=219). The recurrence score was prognostic in the tamoxifen-alone group (p=0·006; hazard ratio HR 2·64, 95% CI 1·33–5·27, for a 50-point difference in recurrence score). There was no benefit of CAF in patients with a low recurrence score (score <18; log-rank p=0·97; HR 1·02, 0·54–1·93), but an improvement in disease-free survival for those with a high recurrence score (score ≥31; log-rank p=0·033; HR 0·59, 0·35–1·01), after adjustment for number of positive nodes. The recurrence score by treatment interaction was significant in the first 5 years (p=0·029), with no additional prediction beyond 5 years (p=0·58), although the cumulative benefit remained at 10 years. Results were similar for overall survival and breast-cancer-specific survival. Interpretation The recurrence score is prognostic for tamoxifen-treated patients with positive nodes and predicts significant benefit of CAF in tumours with a high recurrence score. A low recurrence score identifies women who might not benefit from anthracycline-based chemotherapy, despite positive nodes. Funding National Cancer Institute and Genomic Health.