Skip to main content
. 2023 Sep 14;29(10):2577–2585. doi: 10.1038/s41591-023-02554-7

Table 1.

Demographic and baseline disease characteristics

Osimertinib-relapsed (n = 45) All-treated population (N = 91)
Median age, years (minimum–maximum) 65 (39–85) 61 (36–85)
Sex
Female 25 (56) 52 (57)
Male 20 (44) 39 (43)
Race
Asian 19 (42) 65 (71)
White 20 (44) 20 (22)
Black 2 (4) 2 (2)
Multiple/not reported 4 (9) 4 (4)
ECOG PS
0 12 (27) 29 (32)
1 33 (73) 62 (68)
History of smoking
Yes 20 (44) 41 (45)
No 25 (56) 50 (55)
Median time from initial diagnosis to first dose, months (minimum–maximum) 32 (5–98) 24 (1–98)
Location of metastasesa
Lymph node 18 (40) 44 (48)
Bone 19 (42) 31 (34)
Brain 13 (29) 30 (33)
Liver 8 (18) 10 (11)
Adrenal gland 4 (9) 4 (4)
Other/not reported 22 (49) 47 (52)
Median prior lines of therapy (minimum–maximum) 2 (1–4) 2 (0–9)
EGFR primary mutation
Exon 19 deletion 30 (67)
Exon 21 L858R 14 (31)
Unknown 1 (2)
Prior systemic therapy 45 (100)
Platinum-based chemotherapyb 7 (16) 18 (20)
EGFR TKIa
1st or 2nd generation 33 (73) 54 (59)
3rd generation 45 (100) 53 (58)
Received as 1st line 12 (27)
Received as 2nd line 33 (73)
No prior therapy 0 23 (25)

Data are number of patients (%) unless otherwise noted.

aPatients could be counted in more than one category.

bSeven patients had limited platinum exposure (<two cycles) given before first EGFR TKI in the osimertinib-relapsed group.