Therapeutic Response

ERBB2 TKD activating variants status confers therapeutic sensitivity to Zongertinib in patients with Lung Non-Squamous Non-Small Cell Carcinoma.

Statements

Source and description

Hernexeos (zongertinib) [package insert]. FDA. The U.S. Food and Drug Administration (FDA) granted approval to zongertinib for the treatment of adult patients with unresectable or metastatic non-squamous non-small cell lung cancer (NSCLC) whose tumors have HER2 (ERBB2) tyrosine kinase domain activating mutations, as detected by an FDA-approved test, and who have received prior systemic therapy. This indication is approved under accelerated approval based on objective response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).