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

被引:435
作者
Mamounas, Eleftherios P. [1 ]
Tang, Gong
Fisher, Bernard
Paik, Soonmyung
Shak, Steven
Costantino, Joseph P.
Watson, Drew
Geyer, Charles E., Jr.
Wickerham, D. Lawrence
Wolmark, Norman
机构
[1] Aultman Hlth Fdn, Canton, OH 44710 USA
关键词
SURGICAL ADJUVANT BREAST; GENE-EXPRESSION; CLINICAL BENEFIT; TAMOXIFEN; CHEMOTHERAPY; MASTECTOMY; PREDICTION; SIGNATURE; PATTERNS;
D O I
10.1200/JCO.2009.23.7610
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 4.3% (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. J Clin Oncol 28: 1677-1683. (C) 2010 by American Society of Clinical Oncology
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页码:1677 / 1683
页数:7
相关论文
共 23 条
[1]  
ALBAIN KS, 2007, BR CANC RES TREAT S, V1, P106
[2]  
[Anonymous], CLIN PRACT GUID ONC
[3]   Genomic prediction of locoregional recurrence after mastectomy in breast cancer [J].
Cheng, Skye H. ;
Horng, Cheng-Fang ;
West, Mike ;
Huang, Erich ;
Pittman, Jennifer ;
Tsou, Mei-Hua ;
Dressman, Holly ;
Chen, Chii-Ming ;
Tsai, Stella Y. ;
Jian, James J. ;
Liu, Mei-Chin ;
Nevins, Joseph R. ;
Huang, Andrew T. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (28) :4594-4602
[4]   Measurement of gene expression in archival paraffin-embedded tissues - Development and performance of a 92-gene reverse transcriptase-polymerase chain reaction assay [J].
Cronin, M ;
Pho, M ;
Dutta, D ;
Stephans, JC ;
Shak, S ;
Kiefer, MC ;
Esteban, JM ;
Baker, JB .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (01) :35-42
[5]  
Dowsett M, 2009, CANCER RES, V69, p75S
[6]   Five versus more than five years of tamoxifen for lymph node-negative breast cancer: Updated findings from the National Surgical Adjuvant Breast and Bowel Project B-14 randomized trial [J].
Fisher, B ;
Dignam, J ;
Bryant, J ;
Wolmark, N .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (09) :684-690
[7]   Tamoxifen and chemotherapy for lymph node-negative, estrogen receptor-positive breast cancer [J].
Fisher, B ;
Dignam, J ;
Wolmark, N ;
DeCillis, A ;
Emir, B ;
Wickerham, DL ;
Bryant, J ;
Dimitrov, NV ;
Abramson, N ;
Atkins, JN ;
Shibata, H ;
Deschenes, L ;
Margolese, RG .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (22) :1673-1682
[8]   Treatment of lymph-node-negative, oestrogen-recept-postive breast cancer: long-term findings from National Surgical Adjuvant Breast and Bowel Project randomised clinical trials [J].
Fisher, B ;
Jeong, JH ;
Bryant, J ;
Anderson, S ;
Dignam, J ;
Fisher, ER ;
Wolmark, N .
LANCET, 2004, 364 (9437) :858-868
[9]   A RANDOMIZED CLINICAL-TRIAL EVALUATING TAMOXIFEN IN THE TREATMENT OF PATIENTS WITH NODE-NEGATIVE BREAST-CANCER WHO HAVE ESTROGEN-RECEPTOR POSITIVE TUMORS [J].
FISHER, B ;
COSTANTINO, J ;
REDMOND, C ;
POISSON, R ;
BOWMAN, D ;
COUTURE, J ;
DIMITROV, NV ;
WOLMARK, N ;
WICKERHAM, DL ;
FISHER, ER ;
MARGOLESE, R ;
ROBIDOUX, A ;
SHIBATA, H ;
TERZ, J ;
PATERSON, AHG ;
FELDMAN, MI ;
FARRAR, W ;
EVANS, J ;
LICKLEY, HL ;
KETNER, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (08) :479-484
[10]   Multicenter validation of a gene expression-based prognostic signature in lymph node-negative primary breast cancer [J].
Foekens, JA ;
Atkins, D ;
Zhang, Y ;
Sweep, FCGJ ;
Harbeck, N ;
Paradiso, A ;
Cufer, T ;
Sieuwerts, AM ;
Talantov, D ;
Span, PN ;
Tjan-Heijnen, VCG ;
Zito, AF ;
Specht, K ;
Hoefler, H ;
Golouh, R ;
Schittulli, F ;
Schmitt, M ;
Beex, LVAM ;
Klijn, IGM ;
Wang, YX .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (11) :1665-1671