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华氏巨球蛋白血症:从生物学特性到治疗方法

Waldenström macroglobulinemia: from biology to treatment.

作者信息

Sahin Ilyas, Leblebjian Houry, Treon Steven P, Ghobrial Irene M

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Expert Rev Hematol. 2014 Feb;7(1):157-68. doi: 10.1586/17474086.2014.871494. Epub 2014 Jan 3.

Abstract

Waldenström macroglobulinemia (WM) is distinct B-cell lymphoproliferative disorder primarily characterized by bone marrow infiltration of lymphoplasmacytic cells along with production of a serum monoclonal (IgM). In this review, we describe the biology of WM, the diagnostic evaluation for WM with a discussion of other conditions that are in the differential diagnosis and clinical manifestations of the disease as well as current treatment options. Within the novel agents discussed are everolimus, perifosine, enzastaurin, panobinostat, bortezomib and carfilzomib, pomalidomide and ibrutinib. Many of the novel agents have shown good responses and have a better toxicity profile compared to traditional chemotherapeutic agents, which makes them good candidates to be used as primary therapies for WM in the future.

摘要

华氏巨球蛋白血症(WM)是一种独特的B细胞淋巴增殖性疾病,主要特征是骨髓中淋巴细胞浆细胞浸润以及血清单克隆(IgM)的产生。在本综述中,我们描述了WM的生物学特性、WM的诊断评估,并讨论了鉴别诊断中的其他疾病、该疾病的临床表现以及当前的治疗选择。所讨论的新型药物包括依维莫司、哌立福辛、恩杂鲁胺、帕比司他、硼替佐米和卡非佐米、泊马度胺和伊布替尼。与传统化疗药物相比,许多新型药物已显示出良好的疗效且毒性特征更佳,这使其成为未来作为WM一线治疗药物的良好候选者。

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