School of Biotechnology, Institute of Science, Banaras Hindu University, Varanasi, 221005, Uttar Pradesh, India.
Mol Cell Biochem. 2023 May;478(5):1013-1029. doi: 10.1007/s11010-022-04576-0. Epub 2022 Oct 10.
Modern clinical therapy of chronic myeloid leukemia (CML) with TKIs is highly efficacious in most CML patients, while it is not remedial and generally confined due to intolerance or resistance. CML is currently considered a severe disease. Interestingly, stem cell transplantation in the past decade was an attractive clinical therapeutic option in CML patients, but it is not successful due to independently more death rates in older patients. So, the targeting of BCR::ABL oncoprotein is extensively used to enhance the reduction in a higher percentage of CML patients by tyrosine kinase inhibitors (TKIs). However, resistance or intolerance responses to these inhibitors are responsible for future deterioration and further development of disease. At this point, the clinical treatment of CML is a major challenge, and the lack of molecular responses to TKIs are not succeeded with chemotherapy alone. So, the considerable efficacious clinical necessities remain unmet. Therefore, continuous efforts are needed to explore new potential treatment strategies with an increasing understanding of CML biology. Therefore, this review deals with the investigation of TKI treatment with interferon, chemotherapy (Hydroxyurea, Homoharringtonine, Omacetaxine, Cytarabine), and several other new TKIs under beneficial clinical trials. Additionally, the approaches towards TKIs-resistant or intolerant CML cells where the respective signaling pathway gets up-regulated are also targeted with its inhibitor. This review presents evidence that new TKIs under clinical and pre-clinical trials may improve the chemotherapy of CML.
目前,慢性髓性白血病(CML)的现代临床治疗采用 TKI 治疗,对大多数 CML 患者非常有效,但由于不耐受或耐药,通常无法治愈且受限。CML 目前被认为是一种严重的疾病。有趣的是,过去十年间,干细胞移植在 CML 患者中是一种有吸引力的临床治疗选择,但由于老年患者的死亡率独立更高,因此并不成功。因此,靶向 BCR::ABL 癌蛋白被广泛用于增强酪氨酸激酶抑制剂(TKI)使更多 CML 患者的缓解率更高。然而,对这些抑制剂的耐药或不耐受反应导致疾病的未来恶化和进一步发展。此时,CML 的临床治疗是一个主要挑战,并且单独使用化疗无法克服对 TKI 的分子反应不足。因此,相当有效的临床需求仍然未得到满足。因此,需要不断努力,通过深入了解 CML 生物学,探索新的潜在治疗策略。因此,本综述探讨了 TKI 与干扰素、化疗(羟基脲、高三尖杉酯碱、奥马环素、阿糖胞苷)以及其他几种新 TKI 在有益临床试验中的联合治疗。此外,还针对各自信号通路上调的 TKI 耐药或不耐受 CML 细胞的靶向治疗策略及其抑制剂。本综述提供的证据表明,在临床和临床前试验中,新的 TKI 可能会改善 CML 的化疗效果。