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. 2021 Sep 25;2(10):100223. doi: 10.1016/j.jtocrr.2021.100223

Table 2.

Therapy Outcomes

Case IHC FISH RNA NGS Variant DNA NGS RNA ISH First-Line Therapy Documented Progression Second-Line Therapy Follow-Up (mo)
1 P P EML4 (ex 13)–ALK (ex 20) 1 N P Alectinib N 4
2 P P EML4 (ex 13)–ALK (ex 20) 1 N P Alectinib N 9
3 P P EML4 (ex 6)–ALK (ex 20) 3 a/b N P Alectinib N 10
4 P P EML4 (ex13)- ALK (ex20) 1 N P Alectinib N 10
5 P P EML4 (ex 13)–ALK (ex 20) 1 N P Alectinib N 6
6 P P EML4 (ex 6)–ALK (ex 20) 3 a/b F1174L P Alectinib @ 4 mo, 12 d Lorlatinib 6
7 P P EML4 (ex 13)–ALK (ex 20) 1 N P Alectinib N 13
8 P P EML4 (ex 20)–ALK (ex 20) 2 Na P Crizotinib @ 5 mo Ceritinib 21
9 N P N STK11 N Alectinib @ 3 mo, 5 d Pembrolizumab
Carboplatin-pemetrexed
18
10 P P SLMAP (ex 12/13)–ALK (ex 20) N P Crizotinibb N 24

@, at the rate; ex, exon; FISH, fluorescence in situ hybridization; IHC, immunohistochemistry; N, negative; NGS, next-generation sequencing; P, positive; RNA ISH, RNA in situ hybridization; SGA, single-gene analysis.

a

SGA KRAS/EGFR.

b

Patient initially received cisplatin and pemetrexed for four cycles, after RNA NGS testing ALK fusion was identified and patient was switched to crizotinib.