Breccia Massimo, Alimena Giuliana
Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.
Mediterr J Hematol Infect Dis. 2014 Jan 2;6(1):e2014003. doi: 10.4084/MJHID.2014.003.
With the advent of target therapies, imatinib became the mainstay for treatment of chronic myeloid leukemia. However, despite the brilliant results obtained with this drug, more than 30% of patients discontinue therapy in long-term due to several reasons, including failure and/or intolerance. Second-generation tyrosine kinase inhibitors (TKIs) are more potent drugs and have expanded inhibition against a broad spectrum of mutations resistant to imatinib. Both nilotinib and dasatinib have demonstrated in vitro and in vivo clinical activity against different types of mutations and various forms of resistance. However, patients with T315I mutation do not obtain an advantage from these drugs and a third generation inhibitor ponatinib, a pan-BCR drug, was tested with significant results. In this review, we report the results of second-and third-generation TKIs tested as second or third line therapy in patients resistant and/or intolerant to previous inhibitors.
随着靶向治疗的出现,伊马替尼成为治疗慢性髓性白血病的主要药物。然而,尽管使用这种药物取得了显著疗效,但超过30%的患者由于多种原因,包括治疗失败和/或不耐受,长期中断治疗。第二代酪氨酸激酶抑制剂(TKIs)是更强效的药物,对多种耐伊马替尼的突变具有更广泛的抑制作用。尼洛替尼和达沙替尼在体外和体内均已证明对不同类型的突变和各种耐药形式具有临床活性。然而,携带T315I突变的患者无法从这些药物中获益,一种第三代抑制剂普纳替尼,一种泛BCR药物,经测试取得了显著效果。在本综述中,我们报告了第二代和第三代TKIs作为二线或三线治疗,用于对先前抑制剂耐药和/或不耐受患者的测试结果。