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. Author manuscript; available in PMC: 2024 Jul 1.
Published in final edited form as: Lung Cancer. 2023 May 13;181:107250. doi: 10.1016/j.lungcan.2023.107250

Table 1.

Clinical, pathological characteristics and response to EGFR TKIs of patients with tumors harboring EGFR exon 19 insertion mutations: K745_E746insIPVAIK and others.

Case number Ref. (number) EGFR mutation/histology EGFR TKI (line of therapy) Dose Response RECI ST Percent change target lesion(s) PFS (months) OS(months from start of EGFR TKI) sex/age(years)/ethnicity/PS smoking history (pack-years)
1 25 I740_K745dupI PVAIK*/adenocarcinoma Icotinib (1st) NA PR NA 13 NA M/74/Asian/NA NA
2 31 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) 250 mg PR − 43.7% 4 10 M/68/Asian/NA 50
3 31 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) 250 mg SD NA 5 NA F/51/Asian/NA 0
4 33 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) NA PR NA 5 9 F/42/Asian/NA 0
5 36 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) 250 mg PR -70% 5 NA F/56/white/NA 0
6 36 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (2nd) 250 mg SD NA >9 NA F/48/white/NA 0
7 36 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) 250 mg SD NA >11 NA F/54/white/NA 0
8 27 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) 250 mg PR NA 12 18 F/48/white/2 0
9 33 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (2nd) NA SD NA 22 32 M/46/Asian/NA 15
10 37 I744_K745insKIPVAI*/adenocarcinoma Gefitinib (1st) NA SD NA 24 NA F/37/Asian/NA 0
11 33 I744_K745insKIPVAI*/adenocarcinoma Erlotinib (2nd) NA PD NA 2 11 F/47/Asian/NA 0
12 26 delI744_K745in sKIPVAI*/adenocarcinoma Erlotinib (2nd) 150 mg PR NA 7 9 F/36/white/NA NA
13 current BIDM C K739_I744dup KIPVAI*/adenocarcinoma Erlotinib (1st) 150 mg PR − 30.4% 7 11 F/59/white/3 0
14 current BIDM C K739_I744dup KIPVAI*/adenocarcinoma Erlotinib (2nd) 100 mg PR − 31.2% 8 12 F/68/white/0 10
15 34 K745_E746insI PVAIK/adenocarcinoma Erlotinib (1st) 150 mg PR NA 9 NA F/39/Arab/3 0
16 37 E746_L747insV PVAIK/adenocarcinoma Erlotinib (1st) NA PR NA 16 NA F/60/Asian/NA 0
17 29 I740_K745dupI PVAIK*/adenocarcinoma Erlotinib (3rd) 150 mg PR NA 16 >48 F/39/white/NA 0
18 28 K745_E746insI PVAIK/adenocarcinoma Erlotinib (1st) 150 mg SD NA 18 24 F/55/Asian/1 0
19 19 K745_E746ins PVAIK/adenocarcinoma Erlotinib (1st) NA PR NA 19 NA NA NA
20 19 K745_E746insIPVAIK/adenocarcinoma Erlotinib (1st) NA PR NA 50 NA NA NA
21 35 K745_E746insIPVAIK/adenocarcinoma Afatinib (1st) 40 mg PD NA 1 4 F/75/Asian/1 NA
22 30 I740_K745dupIPVAIK*/adenocarcinoma Afatinib (2nd) 30 mg PR NA 13 21 M/63/Asian/NA 45
23 19 K745_E746insI PVAIK/adenocarcinoma Afatinib (1st) NA PR NA 14 NA NA NA
24 38 I740_K745dupI PVAIK*/NSCLC NOS Osimertinib (1st)+bevacizumab NA PR NA >1 NA F/58/Asian/NA NA
25 38 I740_K745dupI PVAIK*/NSCLC NOS Osimertinib (1st) NA PR NA >2 NA F/67/Asian/NA 0
26 current BIDM C K745_E746insI PVAIK/adenocarcinoma Osimertinib (1st) 80 mg PR − 31.6% 9 >13 F/73/white/0 2

EGFR, epidermal growth factor receptor; PS, ECOG performance status; TKI, tyrosine kinase inhibitor; RECIST, Response evaluation in solid tumors version 1.1; PR, partial response; SD, stable disease; PD, progressive disease; PFS, progression-free survival; OS, overall survival; NSCLC NOS, non-small-cell lung cancer not otherwise specified; NA, not available; +, ongoing survival for PFS or OS. For OS, it was assumed survival was ongoing (>) when report did not specify otherwise. When extrapolating from written or graphic data from publications, we rounded response change or months to nearest full value. * indicates mutations that have the same amino-acid sequence as EGFR-K745_E746insIPVAIK