Patient Demographics and Outcomes
Patient Identifier | Gender | Age | Disease Site | Previous Therapy | Baseline Tumor Mutationa | Trial Armb | Best Clinical outcomec | Overall Survivald | Progression Free Survivald |
---|---|---|---|---|---|---|---|---|---|
1 | F | 82 | Skin | Temodar 3 cycles (1.5 yrs. prior) | BRAF V 600 K | OBS | PD | 6.3 | 3.2 |
2 | M | 74 | Skin and chest wall | IL-2, IFNα, ipilimumab | BRAF V600E and NRAS | NR | PD | 14.0 | 2.0 |
3 | F | 82 | Skin | – | NRAS Q61R | NR | PD | 13.6 | 2.1 |
4 | M | 74 | Skin | – | None | NR | PD | 1.0 | 0.8 |
5 | M | 44 | Skin and brain | – | BRAF V600E | NR | PD | 0.6 | 0.4 |
6 | M | 67 | Nasal cavity | IFNα, vaccine + ipilimumab, IL-2 | None | IFN | SD | 39.8 | 5.5 |
7 | M | 42 | Skin and lymph nodes | Ipilimumab, dacarbazine, IFNα, carboplatin + paclitaxel (2 mo. prior), pembrolizumab | None | OBS | SD | 20.0 | 7.2 |
8 | F | 74 | Skin | IFNα, DC vaccine, ipilimumab, pembrolizumab (11–090) | None | IFN | SD | 13.0 | 8.7 |
9 | M | 66 | Skin and lymph nodes | IFN, ipi, anti-PD-1 | NRAS Q61K | IFN | SD | 27.4 | 5.7 |
10 | M | 61 | Skin and retroperitoneum | Ipilimumab | NRAS | OBS | PR | 44.3 | 13.4 |
11 | M | 56 | Skin and lymph nodes | IFNα, ipilimumab, IL-2, dacarbazine | None | NR | PD | 14.8 | 1.7 |
12 | M | 44 | Lymph nodes | – | NRAS | OBS | SD | 41.7 | 3.9 |
13 | M | 74 | Skin | IFNα | None | OBS | NED | 42.5 | 18.4 |
14 | F | 58 | Skin | IFNα | BRAF V600E | NR | PD | 28.4 | 1.7 |
15 | F | 52 | Skin | Ipilimumab | NRAS | IFN | NED | 42.7 | 6.9 |
16 | F | 75 | Vulva | IFNα | None | IFN | NED | 38.6 | 9.3 |
17 | M | 64 | Lymph nodes | IFNα, ipi, IL-2 + anti-VEGF | BRAF V600E | NR | PD | 4.6 | 2.3 |
18 | M | 68 | Skin | IFNα | None | OBS | NED | 39.9 | 5.0 |
19 | M | 64 | Skin | IFNα, DC vaccine | None | OBS | SD | 3.5 | 3.2 |
20 | M | 60 | Skin | – | None | IFN | PR | 40.1 | 7.3 |
21 | F | 61 | Skin | IFNα | None | OBS | NED | 20.2 | 19.2 |
22 | F | 70 | Lymph nodes | Ipi + IFNα | None | OBS | PD | 3.0 | 2.0 |
23 | M | 28 | Lung | IL-2 + anti-VEGF | None | NR | PD | 11.2 | 2.1 |
24 | F | 42 | Muscle | Ipi + Nivo, IL-2 | None | OBS | PD | 3.2 | 2.1 |
25 | M | 52 | Skin and lymph nodes | – | BRAF V600K | NR | PD | 0.6 | 0.6 |
26 | M | 60 | Skin | IFNα | BRAF V600E | OBS | NED | 36.1 | 3.6 |
27 | F | 59 | Skin | – | n.t. | OBS | NED | 35.8 | 13.7 |
28 | M | 47 | Lymph nodes | IFNα, Nivo, Ipi | BRAF V600E | NR | PD | 11.8 | 1.6 |
29 | M | 60 | Skin | – | n.t. | IFN | NED | 32.3 | 14.0 |
30 | F | 45 | Skin | – | None | IFN | NED | 37.5 | 37.5 |
31 | M | 66 | Skin | IFNα | None | OBS | NED | 37.3 | 30.7 |
32 | F | 41 | Skin | IFNα | n.t. | OBS | NED | 26.5 | 2.5 |
33 | F | 46 | Lower limb and breast | IFNα, Ipi, IL-2, Pembro | BRAF V600E | NR | PD | 1.6 | 0.9 |
34 | M | 88 | Nasal cavity and lung | IFNα, Ipi, Pembro | None | OBS | SD | 8.2 | 3.3 |
35 | F | 52 | Skin and lymph node | GM-CSF (14 yrs. prior), IL-2, ipi | BRAF V600E | IFN | SD | 24.2 | 13.0 |
aTumor mutations identified in available baseline samples tested by clinical pathology sequencing test and/or by NanoString SNV panel, “n.t.” not tested, “None” tested and no mutation detected in panel
bTrial arm: NR not randomized due to early progression, IFN randomized to IFN, OBS randomized to observation
c PD progressive disease, SD stable disease, PR partial response, NED no evidence of disease (all by RECIST)
dTime in months