Table 1.
Molecules | Trial | N | Population | mOS | mPFS | ORR | DCR | Comments |
---|---|---|---|---|---|---|---|---|
Sorafenib | SHARP [18] | 602 |
First-line Versus placebo |
10.7 m | 5.5 m | 2% | 43% | |
ASIAPACIFIC [19] | 226 |
First-line Versus placebo |
6.5 m | 2.8 m | 3.3% | 35.3% | ||
Lenvatinib | REFLECT [20] | 954 |
First-line Versus sorafenib |
13.6 m | 8.9 m | 24.1, 1%CR | 75.5% | |
Regorafenib | RESORCE [21] | 573 |
Second-line Versus placebo |
10.6 m | 3.2 m | 11% | 65% | Exclusion of patients previously intolerant to sorafenib |
Cabozantinib | CELESTIAL [22] | 707 |
Second or third-line Versus placebo |
10.2 m | 5.2 m | 4% | 64% | Inclusion of patients previously intolerant to sorafenib |
Ramucirumab | REACH-2 (35) | 292 |
Second-line Versus placebo |
8.5 m | 2.8 m | 4.6% | 59.9% | Inclusion of patients with poor prognosis based on high alpha-foeto-protein levels |
CR complete response; DCR disease control rate; m months; mOS median overall survival; mPFS median progression-free-survival; N number of randomized patients; ORR objective response rate