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急性淋巴细胞白血病持续存在的挑战和当前问题

Continuing challenges and current issues in acute lymphoblastic leukemia.

作者信息

Kansagra Ankit, Dahiya Saurabh, Litzow Mark

机构信息

a Division of Hematology and Bone Marrow Transplant , Mayo Clinic , Rochester , MN , USA.

b Division of Blood and Marrow Transplant , Stanford University , Stanford , CA , USA.

出版信息

Leuk Lymphoma. 2018 Mar;59(3):526-541. doi: 10.1080/10428194.2017.1335397. Epub 2017 Jun 11.

Abstract

Conventional cytotoxic chemotherapy used to treat acute lymphoblastic leukemia (ALL) has resulted into high cure rates for pediatric patients, however outcomes for adult patients remain suboptimal. The 5-year overall survival is only 30-40% in adults and elderly patients with ALL compared to 90% in children. We have seen major advances in our understanding and management of ALL related to identification of new cytogenetic and molecular abnormalities and development of novel targeted agents for the treatment of ALL. The addition of tyrosine kinase inhibitors, monoclonal antibodies and novel immune therapies (e.g. bispecific T cell engager [BiTE] and chimeric antigen receptor [CAR] T cells) has resulted in improved outcomes. These new developments are changing the treatment paradigm of adults ALL from a 'one size fits all' approach to a more individualized treatment approach based on immunophenotypic, cytogenetic and molecular features. In this article we review recent diagnostic and therapeutic advances along with the challenges in the treatment of patients with ALL.

摘要

用于治疗急性淋巴细胞白血病(ALL)的传统细胞毒性化疗已使儿科患者获得了较高的治愈率,然而成人患者的治疗效果仍不尽人意。与儿童ALL患者90%的5年总生存率相比,成人和老年ALL患者的5年总生存率仅为30%-40%。在ALL的认识和治疗方面,我们取得了重大进展,这与新的细胞遗传学和分子异常的发现以及治疗ALL的新型靶向药物的开发有关。酪氨酸激酶抑制剂、单克隆抗体和新型免疫疗法(如双特异性T细胞衔接器[BiTE]和嵌合抗原受体[CAR] T细胞)的加入改善了治疗效果。这些新进展正在将成人ALL的治疗模式从“一刀切”的方法转变为基于免疫表型、细胞遗传学和分子特征的更个体化的治疗方法。在本文中,我们回顾了ALL患者治疗方面的最新诊断和治疗进展以及面临的挑战。

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