A large observational study of patients with primary immune thrombocytopenia receiving romiplostim in European clinical practice
Abstrakt
Objective: Romiplostim has maintained long-term platelet counts in patients with immune thrombocytopenia (ITP) for up to 5 yr in clinical studies. This prospective observational study aimed to describe romiplostim utilisation and outcomes in European clinical practice.
Methods: Adults with primary ITP who received romiplostim in routine care were eligible. Results: Three-hundred and forty patients were eligible for analysis, of whom 299 (88%) completed the 2-yr observation period.
The median age was 62 yr, with 43% of patients aged >= 65 yr, and two-thirds of patients initiated romiplostim before splenectomy. The median average weekly dose of romiplostim was 2.8 mu g/kg.
The median baseline platelet count was 20 x 10(9) /L, which increased after 2 wk of romiplostim treatment and remained >50 x 10(9) /L thereafter. After romiplostim initiation, there was a decrease in rates of grade >= 3 bleeding events (from 12 to 2 per 100 patient-years) and ITP-related hospitalisations (from 87 to 33 per 100 patient-years).
The rate of thrombotic events was 2 per 100 patient-years, and bone marrow fibrosis occurred in two patients. Conclusions: Romiplostim dosing, effectiveness and safety in an unselected real-world ITP population seemed comparable with that observed in clinical studies.