Quintás-Cardama A, Kantarjian H, Cortes J
Department of Leukemia, Unit 428, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA.
Drugs Today (Barc). 2012 Mar;48(3):177-88. doi: 10.1358/dot.2012.48.3.1750274.
The clinical outcome for patients with chronic myeloid leukemia in chronic phase (CML-CP) is currently very favorable due to the availability of tyrosine kinase inhibitors (TKIs) that are well tolerated and effectively suppress the constitutively activated BCR-ABL1 kinase that underlies the pathogenesis of this malignancy. Three TKIs -imatinib, nilotinib and dasatinib- have been approved as frontline therapy in CML-CP. Another TKI, bosutinib, inhibits with high potency numerous tyrosine kinases, including BCR-ABL1, Src family of kinases and MAPK, among others. Like nilotinib and dasatinib, bosutinib is a second-generation TKI that inhibits the majority of mutations associated with imatinib resistance, with the exception of T315I. In patients with CML-CP with prior intolerance or resistance to imatinib therapy, bosutinib rendered response rates similar to those observed in the same patient population treated with nilotinib or dasatinib. Preliminary results from the ongoing phase III BELA study in which bosutinib is compared in a randomized fashion to imatinib for patients with newly diagnosed CML-CP have been recently reported. We herein summarize the preclinical and clinical experience of bosutinib in CML.
由于酪氨酸激酶抑制剂(TKIs)的出现,慢性期慢性髓性白血病(CML-CP)患者的临床结局目前非常良好。这些抑制剂耐受性良好,能有效抑制构成该恶性肿瘤发病机制基础的持续激活的BCR-ABL1激酶。三种TKI——伊马替尼、尼洛替尼和达沙替尼——已被批准作为CML-CP的一线治疗药物。另一种TKI博舒替尼能高效抑制多种酪氨酸激酶,包括BCR-ABL1、Src激酶家族和丝裂原活化蛋白激酶(MAPK)等。与尼洛替尼和达沙替尼一样,博舒替尼是第二代TKI,除T315I外,它能抑制大多数与伊马替尼耐药相关的突变。在对伊马替尼治疗不耐受或耐药的CML-CP患者中,博舒替尼的缓解率与使用尼洛替尼或达沙替尼治疗的同一患者群体相似。最近报道了正在进行的III期BELA研究的初步结果,该研究将博舒替尼与伊马替尼以随机方式用于新诊断的CML-CP患者。我们在此总结博舒替尼在CML中的临床前和临床经验。