Characteristic | Number of patients absolute relative | |
---|---|---|
Sex | ||
Female | 11 | 39.3% |
Male | 17 | 60.7% |
Karnofsky performance status (KPS) | ||
90–100% | 22 | 78.6% |
80% | 5 | 17.9% |
70% | 1 | 3.6% |
BRAF Status | ||
BRAF V600-E-Mutation | 14 | 50.0% |
No BRAF V600-E-Mutation | 14 | 50.0% |
Controlled extracranial disease | ||
Yes | 10 | 35.7% |
No | 18 | 64.3% |
RPA class | ||
1 | 6 | 21.4% |
2 | 22 | 78.6% |
3 | 0 | 0% |
Melanoma-molGPA | ||
0.5–1.0 | 2 | 7.1% |
1.5–2.0 | 11 | 39.3% |
2.5–3.0 | 11 | 39.3% |
3.5–4.0 | 4 | 14.3% |
Number of SRS lesions per patient | ||
1 | 13 | 46.4% |
2 | 7 | 25.0% |
3 | 7 | 25.0% |
4 | 1 | 3.6% |
Whole brain radiotherapy | ||
Yes | 4 | 14.3% |
Before first SRS | 1 | 3.6% |
After first SRS | 3 | 10.7% |
No | 24 | 85.7% |
Targeted/ immunotherapy (TT/IT) | ||
BRAFi (Dabrafenib/ Vemurafenib) MEKi (Trametinib) | 2 1 | 7.1% 3.6% |
Anti-CTLA-4 (Ipilimumab) | 2 | 7.1% |
Anti-PD1 (Nivolumab/Pembrolizumab) | 6 | 21.4% |
BRAFi+MEKi (Dabrafenib-Trametinib/ Encorafenib-Binimetinib) | 3 | 10.7% |
BRAFi+MEKi ➔ Anti-PD1 | 1 | 3.6% |
Anti-PD1 + Anti-CTLA-4 (Nivolumab-Ipilimumab) | 7 | 25.0% |
BRAFi+MEKi ➔Triple combination (Pembrolizumab-Dabrafenib-Trametinib) | 1 | 3.6% |
none | 5 | 17.9% |
Concurrent TT/IT | ||
Yes | 20 | 71.4% |
No | 8 | 28.6% |