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2023 World Conference on Lung Cancer (Posters)
EP06.03. Clinical Impact of Next-Generation Sequen ...
EP06.03. Clinical Impact of Next-Generation Sequencing in KRAS-Mutated Non-Small Cell Lung Cancer Patients: a Single-Center Experience - PDF(Slides)
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This study evaluated the clinical impact of next-generation sequencing (NGS) in non-small cell lung cancer (NSCLC) patients with KRAS mutations. The researchers conducted a retrospective chart review of NSCLC patients at a hospital in Greece who received systemic therapy. The KRAS mutations were diagnosed using tumor tissue-based NGS. The clinicopathological characteristics of the patients were analyzed, and co-mutations in genes other than KRAS were also detected.<br /><br />A total of 23 patients were included in the study, with a median age at NSCLC diagnosis of 62 years. The majority of patients were smokers (90.5%), and 69.6% had de novo metastatic disease at the time of diagnosis. Adenocarcinoma was the most common histologic type (95.7%).<br /><br />The KRAS mutations detected in these patients included G12C (52.2%), G12V (26.1%), G12D (13.0%), G12S (4.3%), and G13C (4.3%). Co-mutations in genes other than KRAS, such as MET and TP53, were detected in 69.6% of patients.<br /><br />After a median follow-up of 14.6 months, the median progression-free survival was 13.6 months, and the median overall survival was not reached. This suggests that NGS allowed for the detection of additional genomic alterations with potential clinical significance in the majority of KRAS-mutated NSCLC patients.<br /><br />In conclusion, the use of NGS in KRAS-mutated NSCLC patients can provide valuable information on additional genomic alterations that may have prognostic or predictive significance. These findings contribute to the growing body of evidence supporting the clinical utility of NGS in NSCLC management.
Asset Subtitle
Emmanouil Panagiotou
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Speaker
Emmanouil Panagiotou
Topic
Pathology & Biomarkers: Genetic Biomarkers
Keywords
next-generation sequencing
non-small cell lung cancer
KRAS mutations
retrospective chart review
tumor tissue-based NGS
co-mutations
adenocarcinoma
progression-free survival
genomic alterations
clinical utility
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