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. 2020 Nov 19;5(6):e000985. doi: 10.1136/esmoopen-2020-000985

Table 1.

Patient characteristics and mutational information

Clinical information Total (N=18) Lung (N=12) Non-lung (N=6)
Median age (range) 53 (28–80) 52 (28–70) 62 (49–80)
Sex
 Male 7 (38.9%) 4 (33.3%) 3 (50%)
 Female 11 (61.1%) 8 (66.7%) 3 (50%)
Stage
 IV 9 (50%) 7 (58.3%) 2 (33.3%)
 Unknown 9 (50%) 5 (41.7%) 4 (66.7%)
Treatment
 TKI-involved 10 (55.6%) 9 (75%) 1 (16.7%)
 TKI-exclusive 4 (22.2%) 2 (16.7%) 2 (33.3%)
 Unknown 4 (22.2%) 1 (8.3%) 3 (50%)
Mutation type
 Ex16 deletion 13 (72.2%)* 8 (66.7%)* 5 (83.3%)
 Splice site deletion 2 (11.1%) 1 (8.3%) 1 (16.7%)
 Splice site point mutation 4 (22.2%)* 4 (33.3%)* 0

*One patient harboured both Ex16 deletion and splice site point mutation.

Ex16, exon 16; TKI, tyrosine kinase inhibitor.