The study enrolled patients with advanced or metastatic NSCLC harboring HER2 mutations, amplification, or overexpression who had progressed after ≥1 prior lines of anticancer therapy. After enrollment, participants received treatment with rezetamab plus pertuzumab until disease progression, intolerable toxicity, withdrawal of consent, or other conditions requiring treatment discontinuation.
Patients who meet the following criteria are enrolled: Aged 18-75 years Histologically or cytologically confirmed advanced or metastatic non-small cell lung cancer (NSCLC) (AJCC 9th edition) Pathologically documented HER2 mutation, amplification, or overexpression Received ≥1 prior line of systemic anti-cancer therapy for advanced/metastatic disease Received SHR-A1811 combined with pertuzumab
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Intravenous infusion, q3 week, SHR-A1811 combined with pertuzumab
Progression Free Survival (PFS) by investigator assessment
Time frame: Until progression, assessed up to approximately 2 years
Objective Response Rate (ORR)
Time frame: Two years after the last subject was enrolled in the group
Overall Survival (OS)
Time frame: Until death, assessed up to approximately 3 years
Disease Control Rate (DCR)
Time frame: Two years after the last subject was enrolled in the group
Duration of Response (DOR)
Time frame: Two years after the last subject was enrolled in the group
AE
Time frame: until to 90 days after the last dose,assessed up to approximately 3 years
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