Table 2. 50 mg/d 4 weeks on, 2 weeks off vs. 37.5 mg continuous daily dose regimen of sunitinib in NSCLC.
Sunitinib 50 mg/d 4/2 (n =63) | 37.5 mg/d CDD (n =47) | ||
---|---|---|---|
Efficacy | ORR (%) | 11.1 | 2.1 |
PFS (week) | 12.0 | 12.3 | |
OS (week) | 23.4 | 37.1 | |
Adverse events (%, grade 1-2/3-4) | Fatigue | 41/29 | 43/17 |
Pain | 43/17 | 47/2 | |
Nause/Vomiting | 43/10 | 38/2 | |
Stomatitis | 40/3 | 29/2 | |
Hypertension | 6/5 | 19/9 | |
Hemoptysis | NR | 15/2 | |
Neutropenia | 44/5 | NR/9 | |
Thrombocytopenia | 49/5 | NR/0 |
CDD: continous daily dose; PFS: progression-free survival; OS: overall survival; ORR: objective response rate; NR: not reported.