Table 2.
Sorafenib administration in the safety population (N = 331)
| 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) |
Data are presented as mean ± standard deviation, median (range) or count (percentage). Percentages are presented to 2 significant figures