Cruz-Rodriguez Nataly, Deininger Michael W
Versiti Blood Research Institute, Milwaukee, WI.
Department of Medicine, Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, WI.
Blood. 2025 Feb 27;145(9):931-943. doi: 10.1182/blood.2024026312.
Starting with imatinib, tyrosine kinase inhibitors (TKIs) have turned chronic myeloid leukemia (CML) from a lethal blood cancer into a chronic condition. As patients with access to advanced CML care have an almost normal life expectancy, there is a perception that CML is a problem of the past, and one should direct research resources elsewhere. However, a closer look at the current CML landscape reveals a more nuanced picture. Most patients still require life-long TKI therapy to avoid recurrence of active CML. Chronic TKI toxicity and the high costs of the well-tolerated agents remain challenging. Progression to blast phase still occurs, particularly in socioeconomically disadvantaged parts of the world, where high-risk CML at diagnosis is common. Here, we review the prospects of further improving TKIs to achieve optimal suppression of BCR::ABL1 kinase activity, the potential of combining different classes of TKIs, and the current state of BCR::ABL1 degraders. We cover combination therapy approaches to address TKI resistance in the setting of residual leukemia and in advanced CML. Despite the unprecedented success of TKIs in CML, more work is needed to truly finish the job, and we hope to stimulate innovative research aiming to achieve this goal.
从伊马替尼开始,酪氨酸激酶抑制剂(TKIs)已将慢性髓性白血病(CML)从一种致命的血液癌症转变为一种慢性病。由于能够获得晚期CML治疗的患者预期寿命几乎正常,有人认为CML已成为过去的问题,应该将研究资源转向其他地方。然而,仔细审视当前的CML形势会发现情况更为复杂。大多数患者仍需要终身接受TKI治疗以避免活动性CML复发。慢性TKI毒性以及耐受性良好的药物的高昂成本仍然是挑战。进展至急变期的情况仍会发生,尤其是在世界上社会经济条件不利的地区,那里诊断时高危CML很常见。在此,我们综述进一步改进TKIs以实现对BCR::ABL1激酶活性的最佳抑制的前景、联合不同类别的TKIs的潜力以及BCR::ABL1降解剂的现状。我们涵盖了在残留白血病和晚期CML情况下解决TKI耐药性的联合治疗方法。尽管TKIs在CML治疗中取得了前所未有的成功,但仍需要开展更多工作才能真正完成任务,我们希望激发旨在实现这一目标的创新性研究。