Skip to main content
. Author manuscript; available in PMC: 2018 May 1.
Published in final edited form as: J Thorac Oncol. 2017 Jan 11;12(5):872–877. doi: 10.1016/j.jtho.2017.01.004

Table 2.

Concomitant Genetic Alterations in ROS1-Rearranged NSCLC.

Patient Genes with Alterations Prior Systemic
Therapya
1 ATM, CTNNB1, TP53, DNMT3A Yes
2 TP53 No
6 TP53 No
10 TP53 No
14 TP53, SMAD4, APC No
24 TP53, ROS1 (p.G2032R) Yesb
42 MAP2K4, SF3B1 No
43 TP53 Yes
45 TSC2 No
46 TP53 No
48 KRAS (p.I24N), CTNNB1, TP53 No
49 BAP1, CHEK2 No
50 CTNNB1 Yes
53c KRAS (p.G13D), EGFR (p.C781F), KIT, IDH1 No
54 CDKN2A, TP53 No
55 FLT1, PRKDC, RUNX1 No
57 TP53 No
59 CCND1, ARID1A, CDKN2A/B, FGF19, FGF4, FGF3 No
60 MSH6, CDKN2A No
61 CDKN2A/B No
a

Prior systemic therapy includes chemotherapy and/or crizotinib.

b

This tumor sample was derived post-crizotinib. The pre-crizotinib tumor sample did not harbor the ROS1 G2032R mutation, which is a known crizotinib-resistant mutation.23

c

This tumor sample tested positive for ROS1 rearrangement by FISH, but targeted RNA sequencing did not detect a ROS1 fusion transcript.