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

Table 2.

Expression of the biomarkers in the two Cohorts.

Nivolumab Cohort n (%)
Biomarkers <1% 1%–9% 10%–49% ≥50% ND Positive Total Negative Total
PD-L1 38 (82.6) 4 (8.7) 2 (4.3) 1 (2.2) 1 (2.2) 7 (15.6) 38 (84.4)
PD-L2 38 (82.6) 2 (4.3) 5 (10.9) 1 (2.2) 0 (0.0) 8 (17.4) 38 (82.6)
PD-1 13 (28.3) 8 (17.4) 5 (10.9) 18 (39.1) 2 (4.3) 31 (70.5) 13 (29.5)
B7-H3 40 (87.0) 2 (4.3) 3 (6.5) 1 (2.2) 0 (0.0) 6 (13.0) 40 (87.0)
B7-H4 29 (63.0) 5 (10.9) 4 (8.7) 8 (17.4) 0 (0.0) 17 (27.0) 29 (63.0)
Chemotherapy Cohort n (%)
Biomarkers <1% 1%–9% 10%–49% ≥50% ND Positive Total Negative Total
PD-L1 21 (77.8) 5 (18.5) 1 (3.7) 0 (0.0) 0 (0.0) 6 (22.2) 21 (77.8)
B7-H4 1 12 (44.4) 3 (11.1) 3 (11.1) 9 (33.3%) 0 (0.0%) 15 (55.6) 12 (44.4)

Expression of the potential immune-related biomarkers in the Nivolumab Cohort and in the Chemotherapy Cohort reported into each cut-off category; the evaluable samples from each cohort were then divided between positive (≥1%) and negative (<1%) expression. 1 Total = 99.9% due to approximation.