Topp Zheng Z, Saven Alan
Division of Hematology/Oncology, Scripps Clinic, 10666 N Torrey Pines Rd MS 312, La Jolla, CA 92037, USA.
Expert Rev Hematol. 2014 Oct;7(5):659-69. doi: 10.1586/17474086.2014.951629. Epub 2014 Aug 22.
Hairy cell leukemia (HCL) is an uncommon low grade B cell leukemia that is marked by pancytopenia, splenomegaly, and characteristic cytoplasmic hairy projections. The current standard of care is treatment with purine analogs, like cladribine or pentostatin, which provide a high complete remission rate with a median duration of response of 5 years. Many patients who show initial remission will relapse, and others with refractory disease may show no response. The discovery of the BRAF mutation has created a therapeutic target exploited by oral inhibitors like vemurafenib and dabrafenib. Targeted immunotoxins remain an interesting area of study. The use of the monoclonal antibody rituximab in combination with purine analogs appears to produce even higher responses, often employed to minimize or eliminate residual disease. With our current understanding of B cell signaling pathways, the development of kinase inhibitors appears promising and may change the future therapeutic landscape of this rare disease.
毛细胞白血病(HCL)是一种罕见的低度B细胞白血病,其特征为全血细胞减少、脾肿大以及特征性的细胞质毛状突起。目前的标准治疗方法是使用嘌呤类似物,如克拉屈滨或喷司他丁进行治疗,这些药物可提供较高的完全缓解率,缓解持续时间中位数为5年。许多最初缓解的患者会复发,而其他难治性疾病患者可能无反应。BRAF突变的发现产生了一个治疗靶点,被维莫非尼和达拉非尼等口服抑制剂所利用。靶向免疫毒素仍是一个有趣的研究领域。单克隆抗体利妥昔单抗与嘌呤类似物联合使用似乎能产生更高的反应率,常用于最小化或消除残留疾病。基于我们目前对B细胞信号通路的理解,激酶抑制剂的开发前景广阔,可能会改变这种罕见疾病未来的治疗格局。