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Table 2 Disposition of patients at 12 months

From: Multicenter phase II clinical trial of nilotinib for patients with imatinib-resistant or -intolerant chronic myeloid leukemia from the East Japan CML study group evaluation of molecular response and the efficacy and safety of nilotinib

Status

N = 49

On treatment

37 (75.5%)

Treatment discontinued

12 (24.5%)

 Adverse events

9 (18.4%)

     Thrombocytopenia

5 (10.2%)

     Hyperbilirubinemia

2 (4.1%)

     Heart disease

1 (2.0%)

     Headache

1 (2.0%)

 No molecular response

2 (4.1%)

 Disease progression

1 (2.0%)

Median actual dose intensity, mg/day (range)

651 (198–800)