Table 1.
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
cPD progressive disease, SD stable disease, PR partial response, NED no evidence of disease (all by RECIST)
dTime in months