Table 1

Baseline patient characteristics of the immunotherapy treated NSCLC cohorts

CharacteristicYTMA471 cohort
N (%)
H12O_ITX1 cohort
N (%)
Total56128
Gender
Male28 (50)100 (78.1)
Female28 (50)28 (21.9)
Age
<70 years old30 (53.6)68 (53.1)
≥70 years old26 (46.4)60 (46.9)
Smoking history
Active smoker10 (18)34 (26.6)
Former smoker44 (79)88 (68.7)
Never smoker2 (3.6)6 (4.7)
Histology
Adenocarcinoma41 (73)54 (42.2)
Large-cell carcinoma16 (12.5)
Squamous cell carcinoma9 (16)58 (45.3)
Adenosquamous carcinoma2 (3.6)
NSCLC-NOS4 (7.1)
Stage
III5 (8.9)5 (3.9)
IV51 (91.1)123 (96.1)
Actionable drivers
EGFR/ALK/ROS1/RET alterations1 (1.7)7 (5.4)
No EGFR/ALK/ROS1/RET alterations48 (85.7)63 (49.2)
Unknown genetic alterations7 (12.5)58 (45.3)
Central nervous system metastasis
Yes21 (38)24 (18.7)
No35 (62)104 (81.3)
Liver metastasis
Yes11 (20)25 (19.5)
No45 (80)103 (80.5)
LIPI score
Good9 (16.1)27 (21.1)
Intermediate22 (39.3)54 (42.2)
Poor3 (5.4)42 (32.8)
Unknown22 (39.3)5 (3.9)
PD-L1 TPS by IHC
≥50%15 (26.8)32 (25)
1%–49%20 (35.7)44 (34.4)
<1%11 (19.6)46 (36)
Not evaluable10 (17.9)6 (4.6)
Immunotherapy line
139 (70)20 (15.6)
214 (25)79 (61.7)
≥33 (5.4)29 (12.5)
Type of immunotherapy
Chemotherapy +PD-1 axis blockade22 (39.3)0
Dual PD-1 +CTLA4 blockade1 (1.8)0
Other PD-1 axis-based combinations5 (8.9)0
Single-agent PD-1 axis blockade28 (50)128 (100)
Best response to immunotherapy
Complete or partial response17 (33.5)22 (17.1)
Stable disease22 (39)32 (25)
Progressive disease15 (27)74 (57.8)
Not evaluable10
Clinical benefit group
Clinical benefit36 (64.3)37 (28.9)
No clinical benefit19 (33.9)90 (70.3)
Not evaluable1 (1.8)1 (0.8)
  • CTLA-4, cytotoxic T-lymphocytes-associated protein 4 ; IHC, immunohistochemistry; LIPI, Lung Immune Prognostic Index; NSCLC-NOS, non-small cell lung cancer not otherwise specified; PD-1, programmed cell death protein-1 ; PD-L1, programmed death-ligand 1 ; TPS, Tumor Proportion Score.