梳理毛细胞白血病治疗中无化疗替代方案的数据。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Danielle Brazel, David J Hermel, Alan Saven
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引用次数: 0

摘要

毛细胞白血病(HCL)是一种罕见的惰性淋巴细胞增殖性疾病,对嘌呤类似物治疗反应高度敏感。虽然像克拉德滨和喷他汀这样的药物仍然是标准的一线治疗方法,但它们的长期毒性——尤其是骨髓抑制和免疫功能障碍——已经导致人们对无化疗药物的兴趣日益浓厚。HCL分子特征的最新进展,包括BRAF V600E突变的几乎普遍存在,已经导致了靶向治疗这种疾病的时代。在这篇综述中,我们总结了现有的和新兴的HCL治疗策略,包括BRAF和MEK抑制剂,布鲁顿酪氨酸激酶(BTK)抑制剂,抗cd20单克隆抗体和venetoclax。这些方法为复发/难治性疾病患者和不适合接受传统化疗的患者提供了治疗希望。这些方案还导致微小残留病(MRD)阴性的高比率,可能使我们更接近治愈HCL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Threading through the data for chemotherapy-free alternatives in the treatment of hairy cell leukemia.

Hairy cell leukemia (HCL) is a rare, indolent lymphoproliferative disorder that is highly responsive to purine analog therapy. While agents such as cladribine and pentostatin remain standard front-line therapies, their long-term toxicities-particularly myelosuppression and immune dysfunction-have led to growing interest in chemotherapy-free agents. Recent advances in molecular characterization of HCL, including the near-universal presence of BRAF V600E mutations, have led to an era of targeted therapeutics for the treatment of this disease. In this review, we summarize existing and emerging treatment strategies for HCL, including BRAF and MEK inhibitors, Bruton tyrosine kinase (BTK) inhibitors, anti-CD20 monoclonal antibodies, and venetoclax. These approaches offer therapeutic promise for patients with relapsed/refractory disease and for those ineligible to receive traditional chemotherapy. These regimens also result in high rates of minimal residual disease (MRD) negativity, potentially bringing us closer to the cure for HCL.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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