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Validation of the NSABP/NRG Oncology 8-Gene Trastuzumab-benefit Signature in Alliance/NCCTG N9831.
Pogue-Geile, Katherine L; Song, Nan; Serie, Daniel J; Wang, Ying; Gavin, Patrick G; Kim, Rim S; Tanaka, Noriko; Fumagalli, Debora; Taniyama, Yusuke; Li, Zhuo; Rastogi, Priya; Swain, Sandra M; Mamounas, Eleftherios P; Geyer, Charles E; Wolmark, Norman; Lucas, Peter C; Paik, Soonmyung; Thompson, E Aubrey.
Afiliación
  • Pogue-Geile KL; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Song N; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Serie DJ; Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL, USA.
  • Wang Y; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Gavin PG; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Kim RS; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Tanaka N; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Fumagalli D; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Taniyama Y; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Li Z; Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL, USA.
  • Rastogi P; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Swain SM; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Mamounas EP; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Geyer CE; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Wolmark N; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Lucas PC; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Paik S; NSABP Foundation/NRG Oncology, Pittsburgh, PA, USA.
  • Thompson EA; Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL, USA.
JNCI Cancer Spectr ; 4(5): pkaa058, 2020 Oct.
Article en En | MEDLINE | ID: mdl-33241186
ABSTRACT
Our objective was to validate the NSABP 8-gene trastuzumab-benefit signature, developed and initially validated in NRG Oncology/NSABP B-31 in Alliance/NCCTG N9831. The B-31 and N9831 trials demonstrated the benefit of adding trastuzumab to chemotherapy in the adjuvant setting for HER2+ breast cancer patients. NSABP investigators utilized gene expression profiles of N9831 patients (N = 892) to blindly assign patients to large-, moderate-, or no-trastuzumab benefit groups and then NCCTG investigators assessed the degree of trastuzumab benefit using Cox models adjusted for age, nodes, estrogen receptor/progesterone receptor status, tumor size, and grade. Hazard ratios and 2-sided P values for recurrence-free survival of the predicted large- (n = 387), moderate- (n = 401), and no-benefit (n = 104) groups, based on the 8-gene signature were 0.47 (95% CI = 0.31 to 0.73, P < .001), 0.60 (95% CI = 0.39 to 0.92, P = .02), and 1.54 (95% CI = 0.59 to 4.02, P = .38), respectively (P interaction  = .02), providing validation of the 8-gene signature in an independent study.

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: JNCI Cancer Spectr Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: JNCI Cancer Spectr Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos