Characteristic | Patients, no (%) | |
Age, median (range) in years | 64 (31–81) | |
Sex | Female | 9 (69) |
Male | 4 (31) | |
ECOG | 0 | 10 (77) |
1 | 2 (15) | |
2 | 1 (8) | |
Stage | IIIC | 1 (8) |
IV-M1a | 3 (23) | |
IV-M1b | 1 (8) | |
IV-M1c | 6 (46) | |
IV-M1d | 2 (15) | |
BRAFV600 | Mutation | 5 (39) |
Wild type | 8 (62) | |
Prior lines of systemic therapy | Median (range) | 3 (2–9) |
1 or 2 | 4 (31) | |
>2 | 9 (69) | |
Type of prior treatment | Anti-PD-1 monotherapy | 13 (100) |
Anti-CTLA-4 monotherapy | 12 (92) | |
Anti-PD-1/-CTLA-4 combination | 1 (8) | |
BRAF-/MEK-inhibition | 5 (39) | |
Cytotoxic therapy | 6 (46) | |
Injected lesion at baseline | No of myDC-injected lesions, median (range) | 2 (1–15) |
Tumor stage was determined according to the American Joint Committee on Cancer TNM 8th edition. Cytotoxic therapy included DTIC, temozolomide.
CTLA-4, cytotoxic T-lymphocyte-associated protein 4; ECOG, Eastern Cooperative Oncology Group; myDC, myeloid dendritic cells; PD-1, programmed death-1.