Skip to main content
. 2015 Dec;4(6):820–824. doi: 10.3978/j.issn.2218-6751.2015.12.03

Table 1. List of NSCLC patients with METex14 responded to MET tyrosine kinase inhibitors.

Number Age/gender Smoking status Histology MET exon 14 alterations MET IHC MET amplification Best (duration of) response Reference
1 80/F NS Adeno Splice donor site mutation 3+ Yes CR (>7 months) (PERIST) to cabozantinib Paik et al., Cancer Dis 2015 (16)
2 78/M ES Adeno Splice donor site deletion 3+ NR PR to crizotinib (lung); PD to crizotinib (liver) Paik et al., Cancer Dis 2015 (16)
3 65/M ES Adeno Splice donor site mutation NR NR PR (>7 months) to crizotinib Paik et al., Cancer Dis 2015 (16)
4 90/F NS Adeno Splice donor site mutation NR NR PR (>5 months) to crizotinib Paik et al., Cancer Dis 2015 (16)
5 86/M NS Adeno Splice donor site deletion 2+ NR PR (5 weeks) to crizotinib Jenkins et al., Clin Lung Cancer 2015 (19)
6 71/M ES Adeno Splice donor site mutation “D1028H” NR No PR (>6 months) to crizotinib Waqar et al., J Thorac Oncol 2015 (20)
7 76/F ES Adeno Splice donor site mutation “D1010H” NR No PR (>8 months) to crizotinib Mendenhall et al., J Thorac Oncol 2015 (21)
8 82/F ES Large cell Splice donor site mutation 3+ Yes* PR (>5 months) to capmatinib Frampton et al., Cancer Dis 2015 (17)
9 66/F ES SqCC Splice donor site mutation 3+ NR PR (>13 months) to capmatinib Frampton et al., Cancer Dis 2015 (17)
10 74/F ES Sarcomatoid Splice site mutation NR NR** PR (>2 months) to crizotinib Liu et al., J Clin Oncol 2015 (18)
11 61/M NS Sarcomatoid Splice donor site mutation/H1094Y NR NR PR (> 5 months) to crizotinib Lee et al., J Thorac Oncol 2015 (22)

NSCLC, non-small cell lung cancer; METex14, MET exon 14 deletion; IHC, immunohistochemistry; M, male; F, Female; ES, ever-smoker; NS, never-smoker; Adeno, adenocarcinoma; SqCC, squamous cell carcinoma; NR, not reported; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease. *, MET/CEP7 =2.3 (low amplification); **, polysomy (9 copies) of the MET exon 14 mutation allele.