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EP.12.32 Targeted Therapy Utilization in Patients ...
EP.12.32 Targeted Therapy Utilization in Patients With Stage IV Non-Small Cell Lung Cancer Harboring Actionable Mutations
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This study evaluates the real-world utilization of targeted therapies in U.S. oncology practices among patients diagnosed with stage IV non-small cell lung cancer (NSCLC) harboring actionable genetic mutations, between January 1, 2022, and December 31, 2024. The targeted mutations studied include EGFR (exon 19 deletion and L858R), ALK, ROS1, BRAF V600E, MET exon 14 skipping, RET, NTRK1/2/3, KRAS G12C, and ERBB2. NRG1 was recently added by NCCN guidelines but was not analyzed here.<br /><br />Patients included were adults with newly diagnosed stage IV NSCLC confirmed via manual chart review who started first- or second-line targeted therapies consistent with NCCN version 7.2025 guidelines.<br /><br />Findings show that targeted therapy utilization varies significantly by mutation type. EGFR-mutated patients had the highest targeted therapy use (approximately 90%), followed by ALK (73%), with moderate use among ROS1 and RET mutations (60%). Utilization declined among those with BRAF V600E, MET exon 14 skipping, and NTRK mutations, where only about 60% received appropriate targeted treatments. ERBB2 and NTRK-mutated patients had lower rates, under 50%.<br /><br />Histology influenced treatment receipt: 71% of patients with adenocarcinoma received targeted therapy, compared to only 36% of those with squamous cell carcinoma.<br /><br />The study concludes that despite NCCN recommendations, not all patients with actionable mutations receive targeted therapies. Contributing factors to underutilization, especially in squamous histology and certain rare mutations, require further investigation to improve treatment equity and outcomes in stage IV NSCLC.
Asset Subtitle
Edgardo S. Santos
Meta Tag
Speaker
Edgardo S. Santos
Topic
Metastatic Non-small Cell Lung Cancer – Targeted Therapy
Keywords
stage IV non-small cell lung cancer
NSCLC
targeted therapies
EGFR mutations
ALK mutations
ROS1 mutations
BRAF V600E
MET exon 14 skipping
RET mutations
treatment utilization
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