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2023 World Conference on Lung Cancer (Posters)
P2.12. Response to Emerging Targeted Therapies and ...
P2.12. Response to Emerging Targeted Therapies and Genomic Analysis for NSCLC with Leptomeningeal Metastases and Uncommon Mutations - PDF(Slides)
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This study focused on the clinical and molecular features of advanced non-small cell lung cancer (NSCLC) with leptomeningeal metastases (LM) and uncommon genetic drivers. The researchers identified patients with NSCLC who had uncommon oncogenic alterations, such as atypical EGFR mutations, ROS1/RET fusions, and ERBB2 alteration. They analyzed the clinical outcomes and compared the molecular features of these patients with those who had classical EGFR mutations. <br /><br />The results showed that patients with LM and atypical EGFR mutations or ROS1/RET fusions had improved prognoses compared to those with ERBB2-positive LM. The genomic landscape of atypical EGFR mutations was found to be similar to classical EGFR mutations. Patients with fusions had the longest median overall survival (27.8 months), followed by those with atypical EGFR mutations (8 months) and ERBB2 mutations (4.8 months). The overall survival for patients with ROS1 fusion was longer than those with RET fusion.<br /><br />The researchers also collected cerebrospinal fluids from patients with molecular profiles. They found co-mutations, including TP53, MYC, CDK4, and CDKN2A, in the atypical EGFR mutation group. These co-mutation profiles were similar to those with classical EGFR mutations.<br /><br />Overall, the study highlights the importance of targeted therapies for patients with LM and uncommon genetic drivers. Patients with atypical EGFR mutations or ROS1/RET fusions have better prognoses compared to those with ERBB2-positive LM. The findings contribute to the understanding of the molecular characteristics of NSCLC with LM and uncommon genetic drivers.
Asset Subtitle
Guang-Ling Jie
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Speaker
Guang-Ling Jie
Topic
Metastatic NSCLC: Targeted Therapy - Other
Keywords
non-small cell lung cancer
leptomeningeal metastases
uncommon genetic drivers
atypical EGFR mutations
ROS1/RET fusions
ERBB2 alteration
clinical outcomes
molecular features
genomic landscape
overall survival
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