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. 2024 Jan 18;29(5):e681–e689. doi: 10.1093/oncolo/oyae001

Table 1.

Patient characteristics.

Characteristics All patients
(n = 44)
Age
Median (range) 69 (39-79)
Sex
Male 30 (68.2%)
Female 14 (31.8%)
ECOG-performance status
0 17 (38.6%)
1 24 (54.6%)
2 3 (6.8%)
Stage
III/IV 41 (93.2%)
Recurrence 3 (6.8%)
Oncogenic driver
EGFR mutation positivity 6 (13.6%)
ALK rearranged positivity 0 (0.0%)
Smoking status
Current/former 34 (77.3%)
Never 10 (22.7%)
Histology
Adeno 31 (70.5%)
Squamous 8 (18.2%)
Others 5 (11.4%)
PD-L1 status
<1% 16 (36.4%)
1-49% 19 (43.2%)
≥50% 9 (20.5%)
Metastasis sites
Brain 13 (19.6%)
Liver 3 (6.8%)
Bone 15 (34.1%)
Interval from combined chemoimmunotherapy to RAM + DOC, days
Median (range) 32.5 (14-505)
Previous combined chemoimmunotherapy regimen
Platinum + pemetrexed + pembrolizumab 22 (50.0%)
Platinum + paclitaxel/nab-paclitaxel + pembrolizumab 8 (18.2%)
Platinum + paclitaxel/pemetrexed + bevacizumab + atezolizumab 9 (20.5%)
Platinum + pemetrexed + atezolizumab 2 (4.5%)
Platinum + paclitaxel/nab-paclitaxel + atezolizumab 1 (2.3%)
Platinum + pemetrexed + ipilimumab + nivolumab 2 (4.5%)
Reasons for discontinuation of combined chemoimmunotherapy
Due to progression disease 38 (86.4%)
Due to adverse event 6 (13.6%)