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. 2015 Dec 15;5(1):37–46. doi: 10.1159/000367757

Table 3.

Initial daily sorafenib dose administered to US patients enrolled in GIDEON by TACE subgroup

n (%) No TACE n=318 Group A Prior TACE n=158 Group B Concomitant TACE n=29 Group C Prior and Concomitant TACE n=38
Initial dosea
800 mg/day 182 (57) 86 (54) 14 (48) 17 (45)
400 mg/day 109 (34) 52 (33) 12 (41) 14 (37)
Otherb 26 (8) 20 (13) 3 (10) 7 (18)

Data refer to the safety population (n=563).

a

Missing for 1 patient.

b

Other doses included 100, 200, and 600 mg/day.