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2024 World Conference on Lung Cancer (WCLC) - ePos ...
EP.06G.02 Profiling the Metastatic Potential of No ...
EP.06G.02 Profiling the Metastatic Potential of Non-Small Cell Lung Cancer Patients Based on TP53 Classification
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Jun Lu, an Associate Professor at the Shanghai Chest Hospital, led a study examining the metastatic potential of non-small cell lung cancer (NSCLC) related to TP53 gene classification. The study involved 2,736 patients with stages I to IV NSCLC, using next-generation sequencing (NGS) to analyze tissue samples targeting 68 cancer-related genes. The research aimed to determine the contribution of TP53 mutations and co-mutations to the metastatic potential of the cancer.<br /><br />Participants were divided based on their TP53 mutation status across various NSCLC histopathological subtypes. The study categorized patients into four cohorts: TP53 (Low), TP53 (Medium), TP53 (High), and LUSC (lung squamous cell carcinoma) based on mutation frequency. Notably, more malignant pathological subtypes exhibited higher frequencies of TP53 mutations. For instance, poorly differentiated, metastatic LUAD, and mixed LUAD/LUSC cases had TP53 mutation rates as high as 68-74%, while LUSC subtypes had even higher rates, reaching up to 95%.<br /><br />The analysis highlighted that unique combinations of TP53 co-mutations elevate metastatic potential. In LUAD, combinations like RB1ATM, KRASSTK11, and EGFRKRAS were significant, whereas PIK3CACDKN2A and FGFR1FGF4 co-mutations were notable for LUSC.<br /><br />Conclusively, the study underscored that TP53 co-mutations are pivotal in determining NSCLC's metastatic potential, suggesting that these genetic profiles could be targeted for better therapeutic strategies. The findings emphasize the role of driver gene patterns in enhancing the metastasizing capability of tumors, particularly in patients harboring TP53 mutations.
Asset Subtitle
Jun Lu
Meta Tag
Speaker
Jun Lu
Topic
Pathology and Biomarkers
Keywords
NSCLC
TP53 mutations
metastatic potential
next-generation sequencing
lung cancer
co-mutations
histopathological subtypes
LUAD
LUSC
therapeutic strategies
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