Crazzolara R, Bendall L
Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Tyrol, Ausria.
Curr Cancer Drug Targets. 2009 Feb;9(1):19-31. doi: 10.2174/156800909787314057.
Acute lymphoblastic leukemia (ALL) is a clonal proliferation of early B- and T-lymphocyte progenitors and results in the accumulation of leukemic blasts in the bone marrow and various extramedullary sites. It affects both children and adults, with peak prevalence between the ages of 2 to 5 years. Despite current treatment protocols achieving rapid cytoreduction in the vast majority of patients, serious acute and late complications are frequent and resistance to chemotherapy often develops. In contrast to the successes obtained with pediatric patients, treatment outcomes for adults remain poor with only 40% of patients being long-term survivors. Extensive research in the field of ALL has helped understand the mechanisms that control leukemic cells, facilitating the design of new drugs that specifically interfere with leukemic pathways and overcome chemo-resistance induced by common treatment regimens. Herein, we review the current status of the development of novel anti-leukemic agents, with emphasis on small molecular inhibitors that have already translated into clinical trials and are in the advanced stages of preclinical development. Challenges to successful development of each strategy are discussed.
急性淋巴细胞白血病(ALL)是早期B淋巴细胞和T淋巴细胞祖细胞的克隆性增殖,导致白血病原始细胞在骨髓和各种髓外部位积聚。它影响儿童和成人,发病高峰年龄在2至5岁之间。尽管目前的治疗方案能使绝大多数患者迅速实现细胞减少,但严重的急性和晚期并发症仍很常见,且常出现化疗耐药。与儿科患者取得的成功相比,成人患者的治疗结果仍然很差,只有40%的患者是长期幸存者。ALL领域的广泛研究有助于了解控制白血病细胞的机制,促进了新型药物的设计,这些药物能特异性干扰白血病途径并克服常见治疗方案诱导的化疗耐药。在此,我们综述新型抗白血病药物的研发现状,重点关注已进入临床试验和临床前研发后期阶段的小分子抑制剂。讨论了每种策略成功研发面临的挑战。