Breast Cancer Gene Signature Assay

Identifies patients’ 10 years risk of breast cancer recurrence

Breast Cancer Gene Test
  • pro-fevicon FDA approved; CAP & CLIA accredited test.
  • pro-fevicon This gene signature assay is indicated for use in postmenopausal women with hormone receptor-positive, node-negative (Stage I or II) or node-positive (Stage II or III) early-stage breast cancer to be treated with adjuvant endocrine therapy.
  • pro-fevicon It is powered by nCounter digital technology.
  • pro-fevicon Test used to predict patient’s Risk of Recurrence(ROR).
  • pro-fevicon Test included in international clinical practice guidelines.

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