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Recent advances in the biology and treatment of B-cell acute lymphoblastic leukemia

机译:B细胞急性淋巴细胞白血病的生物学和治疗新进展

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Acute lymphoblastic leukemia (ALL) is a hematologic malignancy arising from precursors of the lymphoid lineage. Conventional cytotoxic chemotherapies have resulted in high cure rates of up to 90% in pediatric ALL, but the outcomes for adult patients remain suboptimal with 5-year survival rates of only 30%–40%. Over the last decade, major advances have been made in our understanding and management of ALL. Identification of new prognostic genomic markers and incorporation of minimal residual diseases’ assessment into therapeutic protocols have improved risk stratification and treatment strategies. The use of pediatric-inspired regimens for adolescent and young adults, and the advent of tyrosine kinase inhibitors and novel targeted therapies, including monoclonal antibodies and chimeric antigen receptor T cells, have redefined the therapeutic paradigm of ALL, and significantly improved the outcomes. In this article, we will provide an overview of the current knowledge regarding the biology and treatment of ALL, and highlight recent diagnostic and therapeutic advances made in this area over the past 5 years.
机译:急性淋巴细胞白血病(ALL)是由淋巴谱系前体引起的血液学恶性肿瘤。常规的细胞毒性化学疗法已使小儿ALL治愈率高达90%,但成年患者的治疗效果仍然欠佳,其5年生存率仅为30%–40%。在过去的十年中,我们对ALL的理解和管理取得了重大进展。鉴定新的预后基因组标记并将最小残留疾病的评估纳入治疗方案,可以改善风险分层和治疗策略。在青少年和年轻人中使用儿科启发疗法,酪氨酸激酶抑制剂和新型靶向疗法(包括单克隆抗体和嵌合抗原受体T细胞)的出现,重新定义了ALL的治疗范例,并显着改善了治疗效果。在本文中,我们将概述有关ALL的生物学和治疗的最新知识,并重点介绍过去5年在该领域取得的最新诊断和治疗进展。

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