Table 3 Final combined AE multivariate models of associations between adverse events and objective response (OR; complete or partial response) for mRCC patients receiving sunitinib on Schedule 4/2 or any dose/schedule
Schedule 4/2 | Any dose/schedule | ||||||
|---|---|---|---|---|---|---|---|
Adverse event at any time point | End point | Odds ratio | 95% CI | P-valuea | Odds ratio | 95% CI | P-valuea |
Neutropenia | OR | 0.53 | 0.35–0.79 | 0.0021 | 0.44 | 0.30–0.66 | <0.0001 |
Hypertension | OR | 0.20 | 0.12–0.34 | <0.0001 | 0.20 | 0.12–0.32 | <0.0001 |
Hand–foot syndrome | OR | 0.43 | 0.27–0.68 | 0.0003 | 0.43 | 0.28–0.66 | 0.0001 |
Asthenia/fatigue | OR | 0.44 | 0.28–0.70 | 0.0005 | 0.48 | 0.32–0.73 | 0.0007 |
Thrombocytopenia | OR | 0.54 | 0.33–0.87 | 0.0118 | 0.55 | 0.35–0.86 | 0.0098 |