未经治疗的慢性粒细胞白血病慢性期患者的初始治疗

Ehab Atallah
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引用次数: 0

摘要

自引入酪氨酸激酶抑制剂以来,慢性髓性白血病(CML)患者的预后发生了显著变化。目前,伊马替尼是唯一获得美国食品和药物管理局批准的用于治疗新诊断的CML患者的酪氨酸激酶抑制剂。使用伊马替尼400mg,在中位随访60个月后,估计83%的患者预计没有疾病进展。尽管这一生存率高于以往任何治疗CML的方法,但仍有改进的空间。为了提高这些结果,研究了新诊断的CML患者的各种治疗方法。其中,大剂量伊马替尼或一种新的酪氨酸激酶抑制剂,即尼罗替尼或达沙替尼,显示出希望。我们的目的是回顾使用不同方法治疗新诊断CML患者的各种研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Initial Therapy in Previously Untreated Patients with Chronic Myelogenous Leukemia in Chronic Phase

The prognosis of patients with chronic myeloid leukemia (CML) has markedly changed since the introduction of tyrosine kinase inhibitors. Currently, imatinib is the only Food and Drug Administration–approved tyrosine kinase inhibitor for the treatment of patients with newly diagnosed CML. With imatinib 400 mg, an estimated 83% of patients are expected to be alive without disease progression, after a median follow-up of 60 months. Although this survival figure is higher than for any other previous therapy in CML, there is still room for improvement. To improve on these results, various approaches in the therapy of newly diagnosed patients with CML were studied. Of these, high-dose imatinib, or one of the new tyrosine kinase inhibitors, ie, nilotinib or dasatinib, shows promise. Our aim is to review the results of various studies using different approaches in the therapy of patients with newly diagnosed CML.

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