Therapeutic Response Statement (Sensitivity)
This therapeutic response statement supports the relationship that ER positive, ERBB2 amplification, PR positive status confers therapeutic sensitivity to Neratinib in patients with Invasive Breast Carcinoma.
The European Medicines Agency (EMA) has authorized neratinib for the extended adjuvant treatment of adult patients with early-stage hormone receptor positive HER2-overexpressed/amplified breast cancer and who completed adjuvant trastuzumab-based therapy less than one year ago.
This statement is based on a regulatory approval from the European Medicines Agency:
Nerlynx is indicated for the extended adjuvant treatment of adult patients with early-stage hormone receptor positive HER2-overexpressed/amplified breast cancer and who completed adjuvant trastuzumab-based therapy less than one year ago.