慢性期慢性髓性白血病(CML)一线治疗的发展前景。

IF 2.7 3区 医学 Q2 HEMATOLOGY Current Hematologic Malignancy Reports Pub Date : 2021-10-01 Epub Date: 2021-10-18 DOI:10.1007/s11899-021-00655-z
Heather R Wolfe, Lindsay A M Rein
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引用次数: 5

摘要

综述目的:慢性髓性白血病(CML)是一种骨髓增殖性肿瘤,其特征是成熟和成熟的粒细胞不受控制的增殖。该疾病的特点是存在易位t(9;22),导致BCR-ABL融合异常。从历史上看,治疗方案包括羟基脲、丁硫丹和干扰素-α (IFN-α),同种异体干细胞移植是唯一潜在的治疗方法。最近,酪氨酸激酶抑制剂(TKIs)的发展已经彻底改变了CML的治疗,并将曾经致命的疾病变成了一种慢性和可控制的疾病。本综述旨在探讨慢性期CML的一线治疗方案,为患者量身定制一线治疗提供建议,并探索该领域的新兴治疗方法。最新发现:第一代TKI伊马替尼于2001年被FDA批准用于CML。随着伊马替尼的批准和成功,第二代和第三代tki被开发出来,提供更深入的反应,更快的反应和不同的毒性特征。在一线环境中有许多选择,为每个患者选择最佳的初始治疗已成为一个更复杂的决定。在为慢性粒细胞白血病患者选择一线治疗方案时,应考虑疾病风险、合并症和治疗目标。
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The Evolving Landscape of Frontline Therapy in Chronic Phase Chronic Myeloid Leukemia (CML).

Purpose of review: Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by uncontrolled proliferation of mature and maturing granulocytes. The disease is characterized by the presence of translocation t(9;22) leading to the abnormal BCR-ABL fusion. Historically, treatment options included hydroxyurea, busulfan, and interferon-α (IFN-α), with allogeneic stem cell transplant being the only potential curative therapy. More recently, the development of tyrosine kinase inhibitors (TKIs) has revolutionized the treatment of CML and turned a once fatal disease into a chronic and manageable disorder. This review aims to discuss the frontline treatment options in chronic-phase CML, provide recommendations for tailoring frontline treatment to the patient, and explore emerging therapies in the field.

Recent findings: The first-generation TKI, imatinib, was FDA approved in 2001 for use in CML. Following the approval and success of imatinib, second- and third-generation TKIs have been developed providing deeper responses, faster responses, and different toxicity profiles. With numerous options available in the frontline setting, choosing the best initial treatment for each individual patient has become a more complex decision. When choosing a frontline therapy for patients with chronic-phase CML, one should consider disease risk, comorbid conditions, and the goal of therapy.

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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: his journal intends to provide clear, insightful, balanced contributions by international experts that review the most important, recently published clinical findings related to the diagnosis, treatment, management, and prevention of hematologic malignancy. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as leukemia, lymphoma, myeloma, and T-cell and other lymphoproliferative malignancies. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided.
期刊最新文献
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