Table 2.
Variable | No. (%) |
---|---|
Macroscopic features | |
TNM stage | |
IB | 1 (3.8) |
IIB | 3 (11.5) |
IIIA | 2 (7.7) |
IIIB | 2 (7.7) |
IV | 18 (69.2) |
Locationa | |
Left lower lobe | 3 (11.5) |
Left upper lobe | 6 (23.1) |
Right lower lobe | 4 (15.4) |
Right upper lobe | 12 (46.2) |
Central | 8 (30.8) |
Peripheral | 18 (69.2) |
Microscopic features | |
Subgroupb | |
Pleomorphic carcinoma | 9 (47.4) |
Spindle cell carcinoma | 7 (36.8) |
Giant cell carcinoma | 2 (10.5) |
Carcinosarcoma | 0 |
Pulmonary blastoma | 0 |
Undetermined | 1 (5.3) |
EGFR mutationc | |
Positive | 2 (18.2) |
Negative | 9 (81.8) |
PD-L1 expressiond | |
High expression (TPS ≥ 50%) | 8 (61.5) |
Low expression (1 ≤ TPS < 50%) | 4 (30.8) |
Negative (TPS < 1%) | 1 (7.7) |
TNM, tumor, node, metastasis; EGFR, epidermal growth factor receptor; PD-L1, programmed death ligand 1; TPS, tumor proportion score.
The dominant lobe could not be determined in one patient because the primary lesion was seen as consolidation in both upper lobes.
Pathologic review and subgroup classification were conducted in 19 patients.
EGFR mutation test was performed in 11 patients.
PD-L1 test was performed in 13 patients.