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Prospective validation of a 21-gene expression assay in breast cancer

  • J. A. Sparano
  • , R. J. Gray
  • , D. F. Makower
  • , K. I. Pritchard
  • , K. S. Albain
  • , D. F. Hayes
  • , C. E. Geyer
  • , E. C. Dees
  • , E. A. Perez
  • , J. A. Olson
  • , J. A. Zujewski
  • , T. Lively
  • , S. S. Badve
  • , T. J. Saphner
  • , L. I. Wagner
  • , T. J. Whelan
  • , M. J. Ellis
  • , S. Paik
  • , W. C. Wood
  • , P. Ravdin
  • M. M. Keane, H. L. Gomez Moreno, P. S. Reddy, T. F. Goggins, I. A. Mayer, A. M. Brufsky, D. L. Toppmeyer, V. G. Kaklamani, J. N. Atkins, J. L. Berenberg, G. W. Sledge
  • Albert Einstein College of Medicine
  • Dana-Farber Cancer Institute
  • Juravinski Cancer Center
  • Sunnybrook Research Institute
  • Loyola University Medical Center
  • University of Michigan, Ann Arbor
  • Virginia Commonwealth University
  • University of North Carolina at Chapel Hill
  • Mayo Clinic in Jacksonville, Florida
  • Duke University Medical Center
  • University of Maryland School of Medicine
  • Wake Forest University School of Medicine
  • National Institute of Health
  • Indiana University Bloomington
  • Vince Lombardi Cancer Clinic
  • Northwestern University
  • Baylor College of Medicine
  • Washington University School of Medicine
  • Allegheny General Hospital
  • Yonsei University College of Medicine
  • Emory University
  • University of Texas at San Antonio
  • Irish Clinical Oncology Research Group
  • Instituto Nacional de Enfermedades Neoplásicas Eduardo Cáceres Graziani
  • Cancer Center of Kansas
  • Fox Valley Hematology and Oncology
  • Vanderbilt University
  • University of Pittsburgh
  • Rutgers Cancer Institute of New Jersey
  • Southeast Clinical Oncology Research Consortium
  • University of Hawaii Cancer Center
  • Indiana University-Purdue University Indianapolis
  • Stanford University

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

1208 Citas (Scopus)

Resumen

Background Prior studies with the use of a prospective-retrospective design including archival tumor samples have shown that gene-expression assays provide clinically useful prognostic information. However, a prospectively conducted study in a uniformly treated population provides the highest level of evidence supporting the clinical validity and usefulness of a biomarker. Methods We performed a prospective trial involving women with hormone-receptor-positive, human epidermal growth factor receptor type 2 (HER2)-negative, axillary node-negative breast cancer with tumors of 1.1 to 5.0 cm in the greatest dimension (or 0.6 to 1.0 cm in the greatest dimension and intermediate or high tumor grade) who met established guidelines for the consideration of adjuvant chemotherapy on the basis of clinicopathologic features. A reverse-transcriptase-polymerase-chain-reaction assay of 21 genes was performed on the paraffin-embedded tumor tissue, and the results were used to calculate a score indicating the risk of breast-cancer recurrence; patients were assigned to receive endocrine therapy without chemotherapy if they had a recurrence score of 0 to 10, indicating a very low risk of recurrence (on a scale of 0 to 100, with higher scores indicating a greater risk of recurrence). Results Of the 10,253 eligible women enrolled, 1626 women (15.9%) who had a recurrence score of 0 to 10 were assigned to receive endocrine therapy alone without chemotherapy. At 5 years, in this patient population, the rate of invasive disease-free survival was 93.8% (95% confidence interval [CI], 92.4 to 94.9), the rate of freedom from recurrence of breast cancer at a distant site was 99.3% (95% CI, 98.7 to 99.6), the rate of freedom from recurrence of breast cancer at a distant or local-regional site was 98.7% (95% CI, 97.9 to 99.2), and the rate of overall survival was 98.0% (95% CI, 97.1 to 98.6). Conclusions Among patients with hormone-receptor-positive, HER2-negative, axillary node-negative breast cancer who met established guidelines for the recommendation of adjuvant chemotherapy on the basis of clinicopathologic features, those with tumors that had a favorable gene-expression profile had very low rates of recurrence at 5 years with endocrine therapy alone.

Idioma originalInglés
Páginas (desde-hasta)2005-2014
Número de páginas10
PublicaciónNew England Journal of Medicine
Volumen373
N.º21
DOI
EstadoPublicada - 19 nov. 2015
Publicado de forma externa

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