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. 2018 Oct 27;145(1):241–251. doi: 10.1007/s00432-018-2779-1

Table 4.

Intratumor heterogeneity of KRAS oncogene point mutations in codon 12 in the group of 31 NSCLC patients harboring this mutation in at least 2 of 5 separate cancer tissue samples obtained after complete tumor resection

Number of patients Fraction of KRAS mutation positive cancer tissue samples Histological diagnosis
SCC/ADC/LCNEC
Number of identified KRAS point mutations in KRAS mutation positive cancer tissue samples
G12D G12V G12C G12A G12S
Patients presenting with intratumor heterogeneity of KRAS oncogene point mutations (n = 14)
 5 5/5 2/3/0 2 3 0 0 0
 3 5/5 3/0/0 3 2 0 0 0
 2 5/5 2/0/0 0 3 2 0 0
 2 5/5 2/0/0 2 0 3 0 0
 1 5/5 1/0/0 2 0 0 0 3
 1 5/5 0/1/0 1 0 4 0 0
Patients not presenting with intratumor heterogeneity of KRAS oncogene point mutations (n = 17)
 10 5/5 4/5/1 5 0 0 0 0
 2 5/5 1/1/0 0 0 0 5 0
 1 5/5 1/0/0 0 5 0 0 0
 2 4/5 0/2/0 4 0 0 0 0
 1 3/5 0/0/1 3 0 0 0 0
 1 2/5 0/1/0 2 0 0 0 0

Intratumor heterogeneity of mutated sequence was noted when at least two different mutated sequences were detected in analyzed samples of cancer tissue. One patient with adenosquamous cell carcinoma who had KRAS point mutation G12D in one of five cancer tissue samples is not shown in the table

NSCLC non-small cell lung cancer, SCC squamous cell carcinoma, ADC adenocarcinoma, LCNEC large cell neuroendocrine carcinoma