Table 1.
Authors | Year | Number of patients | Study design | Dose escalation | Dosing frequency | Grade 3 or 4 adverse events | Maximum tolerated dose |
---|---|---|---|---|---|---|---|
Krop et al38 | 2010 | 24 | Phase I single-arm | 0.3–4.8 mg/kg | Every 3 weeks | Thrombocytopenia, pulmonary hypertension | 3.6 mg/kg every 3 weeks |
Beeram et al39 | 2012 | 28 | Phase I single-arm with additional patients added later at maximum dose | 1.2–2.9 mg/kg | Weekly | Thrombocytopenia | 2.4 mg/kg weekly |