Department of Clinical and Experimental Medicine, University of Catania, Via Santa Sofia, 78, Catania, 95123, Italy.
Center of Experimental Oncology and Hematology, A.O.U. Policlinico Vittorio Emanuele, Via Santa Sofia, 78, 95123, Catania, Italy.
Mol Cancer. 2018 Feb 19;17(1):56. doi: 10.1186/s12943-018-0805-1.
The introduction of ABL Tyrosine Kinase Inhibitors (TKIs) has significantly improved the outcome of Chronic Myeloid Leukemia (CML) patients that, in large part, achieve satisfactory hematological, cytogenetic and molecular remissions. However, approximately 15-20% fail to obtain optimal responses according to the current European Leukemia Network recommendation because of drug intolerance or resistance.Moreover, a plethora of evidence suggests that Leukemic Stem Cells (LSCs) show BCR-ABL1-independent survival. Hence, they are unresponsive to TKIs, leading to disease relapse if pharmacological treatment is discontinued.All together, these biological events generate a subpopulation of CML patients in need of alternative therapeutic strategies to overcome TKI resistance or to eradicate LSCs in order to allow cure of the disease.In this review we update the role of "non ABL-directed inhibitors" targeting signaling pathways downstream of the BCR-ABL1 oncoprotein and describe immunological approaches activating specific T cell responses against CML cells.
ABL 酪氨酸激酶抑制剂 (TKI) 的引入显著改善了慢性髓性白血病 (CML) 患者的预后,他们在很大程度上实现了满意的血液学、细胞遗传学和分子缓解。然而,根据目前欧洲白血病网络的建议,大约 15-20%的患者由于药物不耐受或耐药而无法获得最佳反应。此外,大量证据表明白血病干细胞 (LSCs) 表现出 BCR-ABL1 独立的存活。因此,它们对 TKI 无反应,如果停止药物治疗,会导致疾病复发。所有这些生物学事件导致一小部分 CML 患者需要替代治疗策略来克服 TKI 耐药或消除 LSCs,以允许治愈疾病。在这篇综述中,我们更新了针对 BCR-ABL1 癌蛋白下游信号通路的“非 ABL 定向抑制剂”的作用,并描述了激活针对 CML 细胞的特异性 T 细胞反应的免疫方法。