false
OasisLMS
Catalog
WCLC 2025 - Posters & ePosters
P3.18.10 Efficacy and Safety of Aumolertinib as Ad ...
P3.18.10 Efficacy and Safety of Aumolertinib as Adjuvant Therapy in Resectable Stage IA3 EGFRm NSCLC With High Risk Factors
Back to course
Pdf Summary
This prospective, single-arm Phase II trial conducted in China evaluated the efficacy and safety of aumolertinib as adjuvant therapy in patients with resectable stage IA3 (T1cN0M0) EGFR-mutated non-small cell lung cancer (NSCLC) exhibiting high-risk factors. Thirty patients with pathologically confirmed NSCLC harboring EGFR exon 19 deletion or L858R mutations and presenting high-risk features such as spread through air spaces (STAS) and/or vascular invasion (VI) who underwent complete tumor resection (R0) were enrolled. Eligible patients were aged 18 or older with an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1. Participants received oral aumolertinib at 110 mg once daily for up to three years unless disease recurrence or unacceptable toxicity occurred. The study’s primary objective was to assess the therapeutic benefit and safety profile of aumolertinib as an adjuvant treatment in this specific population. This work builds on emerging evidence supporting targeted EGFR inhibition in early-stage NSCLC with high-risk pathological factors. The authors acknowledged the participation of all patients and their families in the trial. References cited include relevant clinical and translational studies on EGFR-mutant NSCLC treatments. Overall, the trial explores the potential of prolonged aumolertinib therapy to reduce recurrence risk and improve outcomes in resectable stage IA3 EGFR-mutant NSCLC patients, addressing an unmet need for optimized adjuvant strategies in this subgroup.
Asset Subtitle
Baiqin Zhao
Meta Tag
Speaker
Baiqin Zhao
Topic
Clinical Trials in Progress
Keywords
aumolertinib
adjuvant therapy
EGFR-mutated NSCLC
stage IA3 lung cancer
high-risk factors
spread through air spaces (STAS)
vascular invasion (VI)
EGFR exon 19 deletion
L858R mutation
phase II trial
×
Please select your language
1
English