Suppr超能文献

奥地利用来那度胺治疗晚期骨髓纤维化的非研究人群的经验。

Experience with lenalidomide in an Austrian non-study population with advanced myelofibrosis.

机构信息

Innere Medizin IV, Klinikum Wels-Grieskirchen, Grieskirchnerstraße 42, 4600 Wels, Austria.

出版信息

Wien Klin Wochenschr. 2013 Apr;125(7-8):196-9. doi: 10.1007/s00508-013-0345-z. Epub 2013 Mar 28.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验