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. 2013 Dec 23;8(12):e83607. doi: 10.1371/journal.pone.0083607

Table 3. EGFR mutational analysis using Sanger and Next Generation sequencing.

Biopsy Samples Number of mutated cases
Total Mutations   observed
Mutations observed in samples with >40% of neoplastic cells
Mutations observed in samples with <40% of neoplastic cells
Sanger (%) NGS (%) Sanger NGS Sanger NGS Sanger NGS
N=14 3 (21.4)a 6 (42.9)b 4 9 4a 8b 0 1
Del Ex19 2 2 2 2 2 2 0 0
L858R 1 2 1 2 1 1 0 1
Other muts. 1 5 1 5 1 5 0 0
Cytology Samples Number of mutated cases Total Mutations observed Mutations observed in samples with >40% of neoplastic cells Mutations observed in samples with <40% of neoplastic cells
Sanger (%) NGS (%) Sanger NGS Sanger NGS Sanger NGS
N=66 11 (16.7) 18 (27.3)c 11 22 11 14c 0 8d
Del Ex19 8 12 8 12 8 9 0 3
L858R 3 3 3 3 3 3 0 0
Others muts. 0 7 0 7 0 2 0 5
All Samples Number of mutated cases Total Mutations observed Mutations observed in samples with >40% of neoplastic cells Mutations observed in samples with <40% of neoplastic cells
Sanger (%) NGS (%) Sanger NGS Sanger NGS Sanger NGS
N=80 14 (17.5)a 24 (30.0)d 15 31 15a 22c 0 9b

aIn one case double mutations were observed; bin two cases double/multiple mutations were observed; cin four cases double/multiple mutations were observed; din six cases double/multiple mutations were observed. NGS, Next Generation Sequencing; Del Ex19, deletion in exon 19; Other muts, mutations other than exon 19 deletion or L858R.