Treatment outcomes with first-line EGFR tyrosine kinase inhibitors in Vietnamese metastatic NSCLC patients harboring compound EGFR mutations.
Abstract
288 Background: Compound EGFR mutations represent a heterogeneous group of genetic alterations with inferior clinical outcomes. While next-generation sequencing has increased their identification, real-world data on first-line TKI efficacy remain limited in Vietnam. This study aimed to investigate time-to-treatment failure (TTF), overall survival (OS) and associated factors in metastatic compound EGFR-positive NSCLC. Methods: An observational study was conducted at the National Cancer Hospital (Vietnam) in compound EGFR-mutated metastatic lung adenocarcinoma patients between 2018 and 2025. Patients received first-line EGFR-TKIs (1st, 2nd, or 3rd generation). Kaplan-Meier curves of TTF and OS from the start of EGFR-TKIs were plotted. Associated factors were evaluated with hazard ratios estimated using univariable and multivariable Cox models. Results: Of 86 patients, the median age was 63.0 years and 61.6% were male. Most patients (95.3%) had a PS 0-1. Brain and liver metastasis presented in 43.0% and 15.1% of patients, respectively. Compound EGFR mutations were categorized into three subgroups: common plus uncommon (64.0%), double uncommon (27.9%), and de novo T790M compound mutations (8.1%). Afatinib was the most commonly used (n = 41, 47.7%), followed by erlotinib/gefitinib (n = 27, 31.4%), and osimertinib (n = 18, 20.9%). Median TTF (mTTF) was 16.0 (95% CI, 12.8 – 19.2) months. Median OS (mOS) was 23.0 (95% CI, 16.0–30.0) months. TTF was comparable across TKI generations (mPFS: 15.0, 19.0, and 15.0 months for first-, second- and third-generation TKIs, respectively; p = 0.788). Similarly, OS did not differ among groups (mOS: 56.0, 23.0, and 20.0 months, respectively; p = 0.576). In multivariable analysis, PS 2 (HR 5.03, p = 0.008), liver metastases (HR 2.99, p = 0.003), and adrenal metastases (HR 2.77, p = 0.003) were independently associated with shorter TTF. Multivariable analysis showed an inferior OS with smoking history (HR 2.56, p = 0.011), PS 2 (HR 6.67, p = 0.009), and liver metastases (HR 2.84, p = 0.007). Conclusions: In a real-world Vietnamese clinical setting, the efficacy of first-line EGFR-TKIs was demonstrated in metastatic NSCLC patients harboring compound EGFR mutations, with a mTTF of 16.0 months and mOS of 23.0 months. Survival outcomes were comparable across EGFR-TKI generations. Poor performance status and liver metastasis were independently associated with worse TTF and OS.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (4)
Hoang Bao Ngoc
Vietnam National Cancer Hospital, Hanoi, Viet Nam
Kien Hung Do
Vietnam Nantional Cancer Hospital, Hanoi, Viet Nam
Do Mai Linh
Vietnam National Cancer Hospital, Hanoi, Viet Nam
Van Tai Nguyen
National Cancer Hospital of Viet Nam, Ha Noi, Viet Nam