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. Author manuscript; available in PMC: 2015 May 26.
Published in final edited form as: Nature. 2014 Nov 27;515(7528):568–571. doi: 10.1038/nature13954

Extended Data Table 1.

Demographic and clinical characteristics of patients in the Study and Validation cohorts.

Variable Response Progression p-value*
UCLA Patients (N=46) N=22 N=24
 Male (%) 17 (74%) 19 (79%) >0.99
 Median Age (range) 65 (45–90) 64 (36–86) 0.86£
 Median WBC Count (range) 6.9 (3.9–21.3) 7.1 (4.0–24.8) 0.52
 Median Pre-TX Tumor Burden in cm (range)¥ 8.7 (1.1–32.2) 7.9 (1.1–19.4) 0.9£
 Metastatic Status
  M0 3 (13%) 2 (8%) 0.13£
  M1a 4 (17%) 2 (8%)
  M1b 7 (30%) 6 (25%)
  M1c 8 (35%) 14 (58%)
 Dosing Regimen
  10Q2W 9 (39%) 5 (21%) 0.2
  10Q3W 8 (35%) 8 (33%)
  2Q3W 5 (22%) 11 (46%)
 BRAF Mutation
  Mutant (# not wild type) 7 (30%) 9 (38%) 0.76
 Previous Treatment
  chemotherapy 3 (13%) 5 (21%) 0.7
  BRAF or MEK inhibitor 3 (13%) 5(21%) 0.7
  immunotherapy
   ipilimumab 8 (35%) 13 (54%) 0.25
   other 7 (30%) 9 (38%) 0.76
 Pre TX Biopsy Location
  Subcutaneous 14 (61%) 11 (46%) 0.02£
  Liver 0 8 (33%)
  Lung 5 (22%) 1 (4%)
  Other 3 (13%) 3 (13%)
IGR Patients (N=15) N=10 N=5
 Median Age (range) 55 (26–73) 60 (38–61) 0.77£
 Male (%) 4 (40%) 2 (40%) >0.99
 Metastatic Status
  M0 2 (20%) 0 (0%) 0.51£
  M1a 3 (30%) 1 (20%)
  M1b 0 (0%) 1 (20%)
  M1c 5 (50%) 3 (60%)
 Dosing Regimen
  10Q2W 5 (50%) 2 (40%) 0.62
  10Q3W 3 (30%) 3 (60%)
  2Q3W 2 (20%) 0 (0%)
 BRAF Mutation
  Mutant (# not wild type) 4 (40%) 2 (40%) >0.99
 Previous Treatment
  chemotherapy 2 (20%) 3 (60%) 0.25
  BRAF or MEK inhibitor 2 (20%) 0 (0%) 0.52
  immunotherapy
   ipilimumab 4 (40%) 2 (40%) >0.99
   other 1 (10%) 1 (20%) >0.99