Table 1.
Characteristic/Clinical response | Patients (total n=34) |
Age, median (range) | 61 (41–79) |
Male sex, n (%) | 20 (59) |
ECOG PS score, n (%) | |
0 | 8 (24) |
1 | 17 (50) |
2 | 7 (21) |
3 | 1 |
Unknown | 1 |
IMDC risk score, n (%) | |
0 | 4 (12) |
1 | 12 (35) |
2 | 14 (41) |
3 | 3 (9) |
4 | 1 (3) |
Tissue specimen, n (%) | |
Primary | 24 (71) |
Metastatic | 10 (29) |
Line of therapy, n (%) | |
First line | 4 (12) |
Second line | 15 (44) |
Third line or after | 15 (44) |
Checkpoint inhibitor treatment, n (%) | |
Nivolumab | 31 (91) |
Ipilimumab/Nivolumab | 2 (6) |
Pembrolizumab | 1 (3) |
Number of doses, median (range) | 9.5 (1–56) |
Time on ICI, median (range) | 4.8 months (0–24) |
Follow-up, median (range) | 9.1 months (1–31) |
Best response (n; %) | |
Disease control (n=16; 47%) | |
Complete response | 2 (6) |
Partial response | 5 (15) |
Stable disease | 9 (26) |
Progressive disease (n=18; 53%) | |
Progressive disease | 18 (53) |
Treatment discontinuation reason | |
Disease progression | 24 |
Immune-mediated toxicity | 2 |
ECOG, Eastern Cooperative Oncology Group.