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Table 2 Sorafenib administration in the safety population (N = 331)

From: Safety assessment of sorafenib in Chinese patients with unresectable hepatocellular carcinoma: subgroup analysis of the GIDEON study

Duration of treatment

 Missing

12 (3.6)

  ≤ 4 weeks

21 (6.3)

  > 4 and ≤8 weeks

37 (11)

  > 8 and ≤12 weeks

51 (15)

  > 12 and ≤16 weeks

23 (6.9)

  > 16 and ≤20 weeks

17 (5.1)

  > 20 and ≤24 weeks

19 (5.7)

  > 24 and ≤28 weeks

15 (4.5)

  > 28 weeks

136 (41)

Treatment duration (weeks) for available patients

 Number

319

 Mean ± SD

29.54 ± 24.79

 Median (range)

22.30 (0.1 to 116.1)

Average daily dose (mg)

 Number

204

 Mean ± S D

776.2 ± 83.6

 Median (range)

800 (332 to 818)

Total dose (mg)

 Number

204

 Mean ± SD

133,512.3 ± 115,060.0

 Median (range)

198,350 (800 to 600,800)

Dose intensity (%)

 Number

204

 Mean ± SD

96.5 ± 11.8

 Median (range)

100 (26 to 102)

Actual days on study drug (excluding off days)

 Number

204

 Mean ± SD

171.4 ± 146.3

 Median (range)

127.5 (1 to 751)

Initial sorafenib dose level

 Number

331

 400 mg

4 (1.2)

 600 mg

1 (0.3)

 800 mg

326 (98)

Total subjects with dose interruptions ticked, yes

7 (2.1)

Total subjects with dose modification ticked, yes

27 (8.2)

Total subjects with dose increase, yes

13 (3.9)

Total subjects with dose reduction, yes

21 (6.3)

  1. Data are presented as mean ± standard deviation, median (range) or count (percentage). Percentages are presented to 2 significant figures