rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Tyrosine kinase inhibitors (TKI) targeting mutant EGFR in non-small cell lung cancer (NSCLC) have been successful to control cancer growth, but acquired resistance inevitably occurs, including mutations directly on EGFR, for example, T790M and C797S.
|
29555874 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
C797S Resistance: The Undruggable EGFR Mutation in Non-Small Cell Lung Cancer?
|
30128066 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Targeting L858R/T790M/C797S mutant EGFR is a major challenge in the new-generation EGFR tyrosine kinase inhibitors development for conquering drug resistant NSCLC.
|
31787359 |
2020 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
EGFR SM NSCLC can acquire resistance to osimertinib through development of the EGFR C797S mutation.
|
31377341 |
2019 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Acquired C797S Mutation upon Treatment with a T790M-Specific Third-Generation EGFR Inhibitor (HM61713) in Non-Small Cell Lung Cancer.
|
26749488 |
2016 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Blinded to tumor genotype, this plasma NGS approach detected a broad range of targetable genomic alterations in NSCLC with no false positives including complex mutations like rearrangements and unexpected resistance mutations such as EGFR C797S.
|
26459174 |
2016 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Collectively, compound <b>13</b>, a novel hederagenin-NO donor hybrid with a different chemical structure from those of the current FDA-approved EGFR-targeted anti-NSCLC drugs, may be a promising lead compound for the treatment of NSCLC expressing gefitinib-resistant EGFR with a T790 M mutation or osimertinib-resistant EGFR-LTC with an L858R/T790M/C797S mutation.
|
31718182 |
2019 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
C797S does not occur in TKI-naïve NSCLCs and provide evidence that screening for this mutation before TKIs administration may not be necessary.
|
31243697 |
2019 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In addition, one of these patients, with an EGFR C797S in a lung biopsy was subsequently found to have EGFR C797N in a later biopsy of pleural fluid, highlighting the dynamic multiclonal nature of advanced NSCLC.
|
30481207 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Combination Osimertinib and Gefitinib in C797S and T790M EGFR-Mutated Non-Small Cell Lung Cancer.
|
28843359 |
2017 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Recent Progress of Small-Molecule Epidermal Growth Factor Receptor (EGFR) Inhibitors against C797S Resistance in Non-Small-Cell Lung Cancer.
|
29136465 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
EGFR C797S/G mutation and the same one presented on the same allele with EGFR T790M mutation were the most common mutation feature and played a key role in resistance to osimertinib in Chinese patients with NSCLC.
|
29713646 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
EGFR C797S mutation mediates resistance to third-generation inhibitors in T790M-positive non-small cell lung cancer.
|
27448564 |
2016 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Additionally, Raman difference spectra detected the response of NSCLC cells with T790M EGFR mutation to second- (neratinib) and third-generation (osimertinib) TKIs, and the resistance of cells with T790M/C797S EGFR mutation to osimertinib.
|
30323297 |
2018 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M.
|
25939061 |
2015 |
rs1057519861
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The T790M and C797S mutations of the epidermal growth factor receptor gene (EGFR) confer resistance to first- and third-generation EGFR tyrosine kinase inhibitors (TKIs), respectively, in patients with non-small cell lung cancer (NSCLC) harboring activating mutations of EGFR.
|
28625653 |
2017 |