Lung Neoplasms Clinical Trial
Official title:
Efficacy of EGFR Tyrosine Kinase Inhibitors (EGFR TKIs) in Patients With EGFR-mutated Non-small Cell Lung Cancer Except Both Exon 19 Deletion and Exon 21 L859R: A Retrospective Analysis
Lung cancer is the leading cause of cancer-related death worldwide and is well known to
remain a major health problem. Non-small-cell lung cancer (NSCLC) constitutes more than 80%
of all the cases of lung cancer.
Today, NSCLC can be defined by various molecular criteria. Especially, somatic mutations
within the epidermal growth factor receptor (EGFR) gene itself were discovered in a subset of
NSCLC patients.
Two activating EGFR mutations are in-frame deletion in exon 19 and the substitutions for
L858R in exon 21, which account for 85% of all clinically important mutations related to EGFR
TKI sensitivity.
Besides two activating EGFR mutations, other EGFR mutations in NSCLC have been discovered.
G719 and L861 are reported to have intermediate sensitivity to EGFR TKI. And in-frame
insertions within exon 20 and T790, which are known to be resistant to EGFR TKIs.
However, there are still other EGFR mutations such as E709 and S768 as well as doublet EGFR
mutations are also observed. These rare mutations have not been fully described and data on
their correlation with response to EGFR-TKIs are still unclear.
Research hypothesis Rare EGFR mutations of unknown clinical significance in NSCLC patients,
which are distinguish from mutations such as deletion in exon 19, L858 and insertion in exon
20, have some possibility of EGFR TKI sensitivity.
Rationale for conducting this study It has an opportunity to be shown the efficacy of EGFR
TKIs in patients with rare EGFR mutation in large number of patients in Korea (Asia) during
the short period.
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