Skip to main content
. 2022 Mar;11(3):452–461. doi: 10.21037/tlcr-21-665

Table 4. The post-transformation gene mutations in the 7 patients that had NGS results.

Gene mutations Patient 1 Patient 2 Patient 3 Patient 4 Patient 5 Patient 6 Patient 7
EGFR Exon 19 Deletion X X X X X X
TP53 X X X X X X X
RB1 loss X X X X X
WNK1 X X
APC X X X X
CCNE1 X X X
KMT2C X X
CDK6 X X
NF1 X X
ATRX X X
CARD11 EGFR amp X X
MYC X X
FGFR1 X X
CDKN1B NOTCH1 KIF1B U2AF1L4 LRP1B ACVR1B TSC1 CUL4B TET2 CUX1 MTRR KMT2D X
PIAS4 SRP68 TERT LMNA CBLB RNF139 PTPRT MALT1 RB1 CFTR CRLF2 AMER1 TOP2A SLC47A2 BCLAF1 ZMYM3 HSP90AA1 EGFR Copy number gain X
KIT NKX2-1 NFKBIA BCL2L2 EGFR L858R STAG2 FOXP1 MPL RAC1 DOT1L SMAD3 EGFR L62R MET MAP2K1(MEK1) CIC BRCA2 CHD2 PMS2 ATM X
PPARG CD22 RET BCL6 AKT2 IKZF1 CEBPA FAM46C DAXX KDM6A X
ZRSR2 SMO FOXO1 CHEK2 KDR PIK3CB SMAD4 RANBP2 X
FGFR3 RPTOR ABL2 IRS2 KLHL6 PDGFRB GNAS AURKA PTCH1 SMAD2 FLT3 KDM5A X
KRAS CCND2 HRAS CCND1 PIK3CA GATA6 GPR124 AR ARID1B ESR1 X

WNK1 mutation was found in both patients 1 and 2 that had longer survival period. VUS genes are not shown. NGS, next-generation sequencing; WNK1, WNK lysine deficient protein kinase 1; VUS, variant of undetermined significance.