Baseline patient characteristics among all three adjuvant NY-ESO-1 clinical trials

NCT00821652NCT01079741NCT00124124
N = 22N = 35N = 34
N(%)/Mean(SD)N(%)/Mean(SD)N(%)/Mean(SD)P-Value
Age59.68 (13.60)55.49 (15.16)56.38 (11.82)0.5134
Sex0.2446
 Female9 (40.91)14 (40.00)20 (58.82)
 Male13 (59.09)21 (60.00)14 (41.18)
Thicknessa2.63 (1.64)2.22 (1.84)4.48 (5.63)0.0122
Ulceration0.1916
 Present7 (31.82)11 (31.43)18 (52.94)
 Absent10 (45.45)17 (48.57)14 (41.18)
 Undetermined5 (22.73)7 (20.00)2 (5.88)
AJCC Stage0.0146
 IIB0 (0.00)3 (8.57)7 (20.59)
 IIC1 (4.55)1 (2.86)0 (0.00)
 IIIA5 (22.73)4 (11.43)6 (17.65)
 IIIB5 (22.73)11 (31.43)10 (29.41)
 IIIC4 (18.18)12 (34.29)10 (29.41)
 IV7 (31.82)4 (11.43)0 (0.00)
 Undetermined0 (0.00)0 (0.00)1 (2.94)
Histologic Subtype0.5588
 Nodular6 (27.27)7 (20.00)12 (35.29)
 Superficial Spreading4 (18.18)5 (14.29)7 (20.59)
 Other3 (13.64)2 (5.71)4 (11.76)
 Undetermined9 (40.91)21 (60.00)11 (32.35)
Primary site0.2624
 Anterior Trunk0 (0.00)4 (11.43)6 (17.65)
 Arms3 (13.64)5 (14.29)1 (2.94)
 Head/Neck5 (22.73)3 (8.57)6 (17.65)
 Legs8 (36.36)15 (42.86)12 (35.29)
 Posterior Trunk3 (13.64)6 (17.14)8 (23.53)
 Unknown3 (13.64)2 (5.71)1 (2.94)

amissing values for thickness: NCT00821652: 4; NCT01079741: 5;NCT00124124: 1