Research Article

Real-World Assessment of Clinical Outcomes in Patients with Lower-Risk Myelofibrosis Receiving Treatment with Ruxolitinib

Table 3

Specific adverse events during ruxolitinib treatment.

All patientsIPSS category
Low riskIntermediate-1 risk
%%%

Total patients108100.0025100.0083100.00
Grade 3 or higher thrombocytopenia87.41312.0056.02
Grade 3 or higher anemia2422.22520.001922.89
Ruxolitinib treatment changes due to adverse reactions
 Dose reduction 1917.59312.001619.28
 Temporary therapy interruption10.9314.0000.00
 Therapy discontinuation10.9314.0000.00

IPSS, International Prognostic Scoring System.
Defined as a platelet count < 50 × 109/L at any point after ruxolitinib initiation through last ruxolitinib dose.
Defined as hemoglobin < 8 g/dL at any point after ruxolitinib initiation through last ruxolitinib dose.