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. 2020 Apr;61:167–179. doi: 10.1016/j.semcancer.2019.09.015

Table 1.

Clinical outcomes of NSCLC patients with rare EGFR mutations in exon 18 after EGFRi treatment.

Mutation Study (Reference) EGFR mutation(s), n treated with EGFRi EGFRi used ORR (%) DCR (%) Median PFS, Median OS,
(CR + PR) (CR + PR + SD) months
(95% CI)
months
(95% CI)
E709X Wu & Shih [35] DelE709-T710insD, n = 5 Gefitinib / Erlotinib 50.0% 72.2% 6.2 29.3
E709X complex mutations, n = 13
Kobayashi & Mitsudomi [8] DelE709_T710insD, n = 4 Gefitinib / Erlotinib 25.0% 50.0% NR NR
E709X complex mutations, n = 15 53.0% 86.7% NR NR
G719X Chiu et al. [39] G719X, n = 78 Gefitinib / Erlotinib 36.8% 72.4% 6.3 NR
G719X + L861Q, n = 9 88.9% 100.0% 11.9 NR
G719X + S768I, n = 10 50.0% 100.0%
Kobayashi & Mitsudomi [8] G719X, n = 148 Gefitinib / Erlotinib 65.5% 32.0% NR NR
G719X complex, n = 58 59.0% 89.7% NR NR
Kate et al. [108] G719X, n = 5 Gefitinib / Erlotinib 50.0% NR 9.0 (NE) NR
Xu et al. [40] G719X, n = 14 Gefitinib / Erlotinib / Icotinib 42.9% 78.6% 5.98 (1.53 - 10.42) 19.81 (16.81 - 22.81)
Sequist et al. [21] G719X, n = 4 Neratinib 75.0% 100.0% 12.1 NR
Yang et al. [9] G719X single, n = 8, + G719X complex, n = 6 Afatinib 77.8% NR 13.8 (6.8 - NE) 26.9 (16.4 - NE)
Ahn et al. [112] G719X n = 19 Osimertinib 52.6% NR NR NR
Pooled Beau-Faller et al. [41] Total n = 18: G719X, n = 14, E709X, n = 2, Gefitinib / Erlotinib 7.0% 33.3% 3 (1 - NE) 22 (1 - 44)
rare exon 18 substitutions, n = 2
Passaro et al. [113] Total n = 42: G719X, n = 35, E709X, n = 3, Gefitinib / Erlotinib / Afatinib 31.0% 69.0% 8.3 (4.8 - 11.7) 17 (8.2 - 25.7)
not specified, n = 4

Legend: EGFRi, EGFR inhibitor; ORR, objective response rate; CR, complete response; PR, partial response; DCR, disease control rate; SD, stable disease; PFS, progression-free survival; CI, confidence interval; OS, overall survival; NR, not reported; NE, not estimable.