Table 1.
N (%) | |
---|---|
Age (N = 123) | 62.1 (35.2,84.5) |
Gender (N = 123) | |
Female | 46 (37.4) |
Male | 77 (62.6) |
Race (N = 123) | |
White | 123 (100.0) |
Other | 0 (0.0) |
Serious comorbidities (N = 122)* | |
No | 115 (94.3) |
Yes | 7 (5.7) |
Other comorbidities (N = 122) | |
No | 34 (27.9) |
Yes | 88 (72.1) |
Active autoimmune disease at initiation of immunotherapy (N = 123) | |
No | 43 (35.0) |
Yes | 80 (65.0) |
Stage at diagnosis (N = 122) | |
Early | 21 (17.2) |
Locally advanced | 33 (27.0) |
Metastatic | 68 (55.7) |
Primary site of cancer (N = 123) | |
NSCLC | 77 (62.6) |
Melanoma | 18 (14.6) |
SCLC | 7 (5.7) |
Head and neck | 6 (4.9) |
Urothelial | 4 (3.3) |
Gastrointestinal | 3 (2.4) |
Renal | 3 (2.4) |
Breast | 2 (1.6) |
Merkel cell | 1 (0.81) |
Ovarian | 1 (0.81) |
Sarcoma | 1 (0.81) |
PDL-1 expression (N = 82) | |
Negative | 16 (19.5) |
Positive | 66 (80.5) |
Setting of immunotherapy administration (N = 123) | |
Adjuvant | 9 (7.3) |
Locally advanced/metastatic | 114 (92.7) |
Line of treatment for metastatic setting (N = 113) | |
1st line | 51 (45.1) |
2nd line | 53 (46.9) |
3rd line and beyond | 9 (8.0) |
Immunotherapy agents (N = 123) | |
CTLA4 | 4 (3.3) |
PD-1/PD-L1 | 116 (94.3) |
Combination CTLA4 and PD-1 | 3 (2.4) |
Immune checkpoint inhibitor (N = 122) | |
Pembrolizumab | 50 (40.9) |
Nivolumab | 51 (41.8) |
Atezolizumab | 8 (6.6) |
Durvalumab | 5 (4.1) |
Ipilimumab | 4 (3.3) |
Ipilimumab and nivolumab | 3 (2.5) |
Avelumab | 1 (0.8) |
Monotherapy (N = 122) | |
No | 29 (23.8) |
Yes | 93 (76.2) |
Combined with chemotherapy (N = 122) | |
No | 99 (81.1) |
Yes | 23 (18.9) |
*Including long QT syndrome, uncontrolled or significant cardiac disease, (recent myocardial infarction, congestive heart failure, unstable angina and bradyarrhythmias)
CTLA-4 cytotoxic T-lymphocyte antigen 4, N number, NSCLC non-small cell lung cancer, PD-1 programmed cell death protein 1, PD-L1 programmed death-ligand 1, SCLC small cell lung cancer