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. 2019 Oct 1;8(10):1566. doi: 10.3390/jcm8101566

Table 1.

Clinical and molecular characteristics of the evaluable patients in the Nivolumab Cohort and in the Chemotherapy Cohort. The Chemotherapy Cohort included only chemotherapy-naïve patients affected by non-squamous NSCLC with ECOG PS = 0–1.

Clinical Characteristics Nivolumab Cohort Chemotherapy Cohort
n (%) n (%)
Patients 46 27
Gender
Male 34 (73.9) 20 (74.1)
Female 12 (26.1) 7 (25.9)
Age (year)
Range 44–82 46–81
Median 70 69
Smoking habit
Current 13 (28.3) 12 (44.4) 1
Former 24 (52.2) 12 (44.4) 1
Never 9 (19.5) 3 (11.1) 1
Histology
Non-squamous 35 (76.1) 27 (100.0)
Squamous 11 (23.9) 0 (0.0)
Stage
IIIB 2 (4.4) 0 (0.0)
IV 44 (95.6) 27 (100.0)
ECOG PS
0 17 (37.0) 6 (22.2)
1 26 (56.5) 21 (77.8)
2 3 (6.5) 0 (0.0)
Previous lines of treatment
Range 1–6 -
Median 2 -
EGFR mutation
Yes 3 (8.6) 2,4 1 (3.7) 3
No 32 (91.4) 4 26 (96.3)
ALK rearrangement
Yes 0 (0.0) 4 0 (0.0)
No 35 (100.0) 4 27 (100.0)

1 Total = 99.9% due to approximation. 2 Two patients in the Nivolumab Cohort had exon 19 deletion, whereas one patient had exon 19 deletion in association with exon 20 insertion. 3 One patient in the Chemotherapy Cohort had exon 21 mutation, which was identified after first-line treatment. 4 Molecular screening for epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements in the Nivolumab Cohort was performed in non-squamous NSCLC only (35/46).