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Adjuvant chemotherapy guided by 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
  • , M. P. Goetz
  • , J. A. Olson
  • , T. Lively
  • , S. S. Badve
  • , T. J. Saphner
  • , L. I. Wagner
  • , T. J. Whelan
  • , M. J. Ellis
  • , S. Paik
  • , W. C. Wood
  • , P. M. 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. L. Berenberg, J. Abrams, G. W. Sledge
  • Albert Einstein College of Medicine
  • Dana-Farber Cancer Institute
  • Sunnybrook Research Institute
  • Loyola University New Orleans
  • University of Michigan, Ann Arbor
  • Virginia Commonwealth University
  • University of North Carolina at Chapel Hill
  • Mayo Clinic in Jacksonville, Florida
  • Duke University Medical Center
  • National Cancer Institute (NCI)
  • Indiana University School of Medicine
  • Vince Lombardi Cancer Clinic
  • Northwestern University
  • McMaster University
  • Washington University School of Medicine
  • NSABP Pathology Office
  • Emory University
  • University of Texas at San Antonio
  • Cancer Trials Ireland
  • 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
  • University of Hawaii Cancer Center
  • Indiana University-Purdue University Indianapolis

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2059 Citas (Scopus)

Resumen

BACKGROUND: The recurrence score based on the 21-gene breast cancer assay predicts chemotherapy benefit if it is high and a low risk of recurrence in the absence of chemotherapy if it is low; however, there is uncertainty about the benefit of chemotherapy for most patients, who have a midrange score. METHODS: We performed a prospective trial involving 10,273 women with hormone-receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative, axillary node-negative breast cancer. Of the 9719 eligible patients with follow-up information, 6711 (69%) had a midrange recurrence score of 11 to 25 and were randomly assigned to receive either chemoendocrine therapy or endocrine therapy alone. The trial was designed to show noninferiority of endocrine therapy alone for invasive disease-free survival (defined as freedom from invasive disease recurrence, second primary cancer, or death). RESULTS: Endocrine therapy was noninferior to chemoendocrine therapy in the analysis of invasive disease-free survival (hazard ratio for invasive disease recurrence, second primary cancer, or death [endocrine vs. chemoendocrine therapy], 1.08; 95% confidence interval, 0.94 to 1.24; P = 0.26). At 9 years, the two treatment groups had similar rates of invasive disease-free survival (83.3% in the endocrine-therapy group and 84.3% in the chemoendocrine-therapy group), freedom from disease recurrence at a distant site (94.5% and 95.0%) or at a distant or local-regional site (92.2% and 92.9%), and overall survival (93.9% and 93.8%). The chemotherapy benefit for invasive disease-free survival varied with the combination of recurrence score and age (P = 0.004), with some benefit of chemotherapy found in women 50 years of age or younger with a recurrence score of 16 to 25. CONCLUSIONS: Adjuvant endocrine therapy and chemoendocrine therapy had similar efficacy in women with hormone-receptor-positive, HER2-negative, axillary node-negative breast cancer who had a midrange 21-gene recurrence score, although some benefit of chemotherapy was found in some women 50 years of age or younger.

Idioma originalInglés
Páginas (desde-hasta)111-121
Número de páginas11
PublicaciónNew England Journal of Medicine
Volumen379
N.º2
DOI
EstadoPublicada - 12 jul. 2018
Publicado de forma externa

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    ODS 3: Salud y bienestar

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