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B 细胞急性淋巴细胞白血病的生物学特性与治疗的最新进展

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

作者信息

Hefazi Mehrdad, Litzow Mark R

机构信息

Division of Hematology, Mayo Clinic, Rochester, MN, USA,

出版信息

Blood Lymphat Cancer. 2018 Sep 25;8:47-61. doi: 10.2147/BLCTT.S170351. eCollection 2018.

Abstract

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.

摘要

急性淋巴细胞白血病(ALL)是一种起源于淋巴系前体细胞的血液系统恶性肿瘤。传统的细胞毒性化疗已使小儿ALL的治愈率高达90%,但成年患者的治疗效果仍不理想,5年生存率仅为30%-40%。在过去十年中,我们对ALL的认识和治疗取得了重大进展。新的预后基因组标志物的鉴定以及将微小残留病评估纳入治疗方案,改善了风险分层和治疗策略。针对青少年和年轻成年人采用小儿启发式方案,以及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的治疗模式,并显著改善了治疗效果。在本文中,我们将概述目前关于ALL生物学和治疗的知识,并重点介绍过去5年该领域最近的诊断和治疗进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0432/6467350/9e5263bf4c9a/blctt-8-047Fig1.jpg

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