Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, 13131 Magnolia Drive, 3 East, Rm 3056H, Tampa, FL 33612, United States.
Crit Rev Oncol Hematol. 2013 Dec;88(3):667-79. doi: 10.1016/j.critrevonc.2013.07.017. Epub 2013 Aug 20.
Despite the success of tyrosine kinase inhibitor (TKI) therapy in patients with chronic myeloid leukemia (CML), minimal residual disease persists, requiring indefinite treatment. Accumulated evidence has shown that leukemic stem cells (LSCs) in the bone marrow can survive TKI treatment via downstream BCR-ABL1-independent signaling pathways that are activated by soluble growth factors and interactions with the extracellular matrix in the bone marrow microenvironment. Research efforts have therefore turned to the identification and development of agents that target LSCs, and together with TKIs, have the potential to eradicate CML. A number of such agents are now under clinical investigation, and others are soon to enter early-phase studies. This review examines the pathways, molecular targets, and potential new therapeutics that, with TKIs, may provide an effective "one-two punch" to cure CML.
尽管酪氨酸激酶抑制剂 (TKI) 治疗在慢性髓性白血病 (CML) 患者中取得了成功,但微小残留病灶仍然存在,需要进行无限期的治疗。积累的证据表明,骨髓中的白血病干细胞 (LSCs) 可以通过下游 BCR-ABL1 非依赖性信号通路存活下来,这些信号通路是由可溶性生长因子激活的,并与骨髓微环境中的细胞外基质相互作用。因此,研究工作转向了识别和开发靶向 LSCs 的药物,这些药物与 TKI 一起有可能根除 CML。目前有许多这样的药物正在进行临床研究,其他药物也即将进入早期研究阶段。这篇综述探讨了可能与 TKI 一起提供有效“一击必杀”治疗 CML 的途径、分子靶点和潜在的新疗法。