Innere Medizin IV, Klinikum Wels-Grieskirchen, Grieskirchnerstraße 42, 4600 Wels, Austria.
Wien Klin Wochenschr. 2013 Apr;125(7-8):196-9. doi: 10.1007/s00508-013-0345-z. Epub 2013 Mar 28.
Current literature provides conflicting evidence regarding the efficacy of lenalidomide in patients with myelofibrosis (MF). The aim of this work was to evaluate the efficacy of lenalidomide in patients with MF treated within a named patient program in Austria. A total of 22 patients with MF were treated with lenalidomide in 7 different centres throughout Austria. Median age of patients was 68 years. Primary MF was present in 13 patients. Eight patients had post-polycythemia vera (post-PV) and 1 post-essential thrombocythemia (post-ET) MF. According to the Dynamic International Prognostic Scoring System (DIPSS), all patients were scored within the intermediate-2 or high-risk group. Approximately one-third of patients were treated with 2 or more prior therapies. The overall response rate according to International Working Group (IWG) criteria was 12.5 %. Efficacy of lenalidomide was moderate in this non-study patient population. Limiting factors seemed to be stage of disease and risk profile of patients included in this analysis.
目前的文献提供了相互矛盾的证据,表明来那度胺在骨髓纤维化(MF)患者中的疗效。本研究旨在评估来那度胺在奥地利命名患者计划中治疗的 MF 患者中的疗效。共有 22 名 MF 患者在奥地利的 7 个不同中心接受来那度胺治疗。患者的中位年龄为 68 岁。原发性 MF 存在于 13 例患者中。8 例患者为真性红细胞增多症后(post-PV)和 1 例原发性血小板增多症后(post-ET)MF。根据动态国际预后评分系统(DIPSS),所有患者的评分均处于中-2 或高危组。约三分之一的患者接受了 2 种或更多的既往治疗。根据国际工作组(IWG)标准,总缓解率为 12.5%。在这例非研究患者人群中,来那度胺的疗效为中度。限制因素似乎是疾病的阶段和纳入本分析的患者的风险状况。