Gene Expression and Benefit of Chemotherapy in Women With Node-Negative, Estrogen Receptor–Positive Breast Cancer

American Society of Clinical Oncology (ASCO) - Tập 24 Số 23 - Trang 3726-3734 - 2006
Soonmyung Paik1, Gong Tang1, Steven Shak1, Chungyeul Kim1, Joffre Baker1, Wanseop Kim1, Maureen Cronin1, Frederick L. Baehner1, Drew Watson1, John Bryant1, Joseph P. Costantino1, Charles E. Geyer1, D. Lawrence Wickerham1, Norman Wolmark1
1From the Division of Pathology, Operations Center, and Biostatistical Center, National Surgical Adjuvant Breast and Bowel Project; Department of Biostatistics, School of Public Health, University of Pittsburgh; Department of Human Oncology, Allegheny General Hospital, Pittsburgh, PA; Genomic Health Inc, Redwood City, CA; and University of California, San Francisco, San Francisco, CA

Tóm tắt

Purpose The 21-gene recurrence score (RS) assay quantifies the likelihood of distant recurrence in women with estrogen receptor–positive, lymph node–negative breast cancer treated with adjuvant tamoxifen. The relationship between the RS and chemotherapy benefit is not known. Methods The RS was measured in tumors from the tamoxifen-treated and tamoxifen plus chemotherapy–treated patients in the National Surgical Adjuvant Breast and Bowel Project (NSABP) B20 trial. Cox proportional hazards models were utilized to test for interaction between chemotherapy treatment and the RS. Results A total of 651 patients were assessable (227 randomly assigned to tamoxifen and 424 randomly assigned to tamoxifen plus chemotherapy). The test for interaction between chemotherapy treatment and RS was statistically significant (P = .038). Patients with high-RS (≥ 31) tumors (ie, high risk of recurrence) had a large benefit from chemotherapy (relative risk, 0.26; 95% CI, 0.13 to 0.53; absolute decrease in 10-year distant recurrence rate: mean, 27.6%; SE, 8.0%). Patients with low-RS (< 18) tumors derived minimal, if any, benefit from chemotherapy treatment (relative risk, 1.31; 95% CI, 0.46 to 3.78; absolute decrease in distant recurrence rate at 10 years: mean, −1.1%; SE, 2.2%). Patients with intermediate-RS tumors did not appear to have a large benefit, but the uncertainty in the estimate can not exclude a clinically important benefit. Conclusion The RS assay not only quantifies the likelihood of breast cancer recurrence in women with node-negative, estrogen receptor–positive breast cancer, but also predicts the magnitude of chemotherapy benefit.

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10.1093/jnci/94.21.1626

10.1023/A:1006141703224

10.1023/A:1006197805041

10.1200/JCO.2001.19.6.1865

10.1093/jnci/93.13.979

Carlson RW, Edge SB, Theriault RL: NCCN: Breast cancer. Cancer Control 8:54,2001-61, (suppl 2)

10.1200/JCO.2003.04.576

10.1016/S0140-6736(04)16981-X

10.1016/S0140-6736(05)66544-0

10.1097/00130404-200211000-00010

10.1200/JCO.2004.05.166

10.1016/S0140-6736(03)14023-8

10.1200/JCO.2005.02.0818

10.1016/S0002-9440(10)63093-3

10.1056/NEJMoa041588

10.1093/jnci/89.22.1673

Paik S, Shak S, Tang G, et al: Multi-gene RT-PCR assay for predicting recurrence in node negative breast cancer patients: NSABP studies B-20 and B-14. Breast Cancer Res Treat 82:S10,2003-S11, (abstr 16)

10.1111/j.1365-2559.1991.tb00229.x

10.1080/01621459.1992.10476248

10.1016/0014-2964(78)90238-4

10.1038/bjc.1987.89

10.1038/bjc.1987.88

10.3109/02841869609083960

10.1038/bjc.1998.584

10.1097/00000421-200102000-00002

10.1056/NEJM197806012982203

10.1158/1078-0432.CCR-04-0380

Berry DA, Cirrincione C, Henderson IC, et al: Effects of improvements in chemotherapy on disease-free and overall survival of estrogen-receptor negative, node-positive breast cancer: 20-year experience of the CALGB U.S. Breast Intergroup. Breast Cancer Res Treat 98:S17,2004, (abstr 29)

Albain K, Barlow W, O'Malley F, et al: Concurrent (CAFT) versus sequential (CAF-T) chemohormonal therapy (cyclophosphamide, doxorubicin, 5-fluorouracil, tamoxifen) versus T alone for postmenopausal, node-positive, estrogen (ER) and/or progesterone (PgR) receptor-positive breast cancer: Mature outcomes and new biologic correlates on phase III intergroup trial 0100 (SWOG-8814). Breast Cancer Res Treat 2004 (abstr 37)

10.1586/14737159.5.3.271

10.1038/35021093

10.1073/pnas.0931261100

10.1056/NEJMoa021967

10.1073/pnas.1732912100

10.1016/S1535-6108(03)00132-6

10.1038/nature03799