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PMID: 20005174 Published · ppublish English Journal Article Multicenter Study Research Support, N.I.H., Extramural

Prognostic and predictive value of the 21-gene recurrence score assay in postmenopausal women with node-positive, oestrogen-receptor-positive breast cancer on chemotherapy: a retrospective analysis of a randomised trial.

The Lancet. Oncology ·Vol. 11 ·No. 1 ·2010-01-00 ·Pages 55-65

Albain KS, Barlow WE, Shak S, Hortobagyi GN, Livingston RB, Yeh IT, Ravdin P, Bugarini R, Baehner FL, Davidson NE, Sledge GW, Winer EP, Hudis C, Ingle JN, Perez EA, Pritchard KI, Shepherd L, Gralow JR, Yoshizawa C, Allred DC, Osborne CK, Hayes DF, Breast Cancer Intergroup of North America

Abstract

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. 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. 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 > or =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. 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. National Cancer Institute and Genomic Health.

MeSH Terms
Adult Aged Antineoplastic Combined Chemotherapy Protocols/therapeutic use Biomarkers, Tumor/genetics Breast Neoplasms/chemistry,drug therapy,genetics,mortality,secondary Clinical Trials, Phase III as Topic Cyclophosphamide/therapeutic use Disease-Free Survival Doxorubicin/therapeutic use Female Fluorouracil/therapeutic use Gene Expression Profiling Gene Expression Regulation, Neoplastic Genetic Testing/methods Humans Kaplan-Meier Estimate Lymphatic Metastasis Middle Aged Patient Selection Postmenopause Predictive Value of Tests Proportional Hazards Models Randomized Controlled Trials as Topic Receptors, Estrogen/analysis Recurrence Retrospective Studies Reverse Transcriptase Polymerase Chain Reaction Risk Assessment Tamoxifen/therapeutic use Time Factors Treatment Outcome United States/epidemiology
Chemicals
Biomarkers, Tumor Receptors, Estrogen Tamoxifen Doxorubicin Cyclophosphamide Fluorouracil
Authors & Affiliations
23 authors, click to expand affiliations / ORCID
Albain Kathy S
Loyola University Chicago Stritch School of Medicine, Cardinal Bernardin Cancer Center, Maywood, IL, USA. [email protected]
Barlow William E
Shak Steven
Hortobagyi Gabriel N
Livingston Robert B
Yeh I-Tien
Ravdin Peter
Bugarini Roberto
Baehner Frederick L
Davidson Nancy E
Sledge George W
Winer Eric P
Hudis Clifford
Ingle James N
Perez Edith A
Pritchard Kathleen I
Shepherd Lois
Gralow Julie R
Yoshizawa Carl
Allred D Craig
Osborne C Kent
Hayes Daniel F
Breast Cancer Intergroup of North America
Supplementary Concepts
CAF protocol (Protocol)
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Article Info
Journal
The Lancet. Oncology
Abbr.
Lancet Oncol
ISSN
1474-5488
Published
2010-01-00
Epub
2009-00-10
Pages
55-65
Language
English
Region
England
NLM ID
100957246
PMCID
PMC3058239
Subset
IM
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