Jabbour Elias, Cortes Jorge E, Ghanem Hady, O'Brien Susan, Kantarjian Hagop M
The University of Texas MD Anderson Cancer Center, Department of Leukemia, Unit 428, 1515 Holcombe Blvd, Houston, TX 77030, USA.
Expert Rev Anticancer Ther. 2008 Jan;8(1):99-110. doi: 10.1586/14737140.8.1.99.
Chronic myeloid leukemia (CML) is characterized by the formation of the Philadelphia chromosome and oncogenic signaling by the resulting Bcr-Abl fusion protein. Understanding the molecular basis of CML has led to the development of highly effective targeted therapies that block Bcr-Abl tyrosine kinase activity. Imatinib, the current first-line therapy for CML, induces durable treatment responses in most patients. However, patients may develop imatinib resistance, which is often due to BCR-ABL mutations. With the availability of second generation tyrosine kinase inhibitors, an effective therapeutic option other than stem cell transplantation is available following imatinib failure. Randomized trial data suggest that dasatinib treatment is superior to imatinib dose escalation in patients with imatinib resistance. Nilotinib, a recently approved analogue of imatinib, has also demonstrated encouraging treatment responses in patients with imatinib-resistant CML. Other agents (including bosutinib and INNO-406) are in clinical development. With the potential availability of multiple treatment options for patients with CML, it may be possible to tailor treatment according to individual patient or disease characteristics, for example, BCR-ABL mutations. Future CML treatment may involve combination strategies. Overall, targeted agents have significantly improved the prognosis of patients diagnosed with CML.
慢性粒细胞白血病(CML)的特征是形成费城染色体以及由此产生的Bcr-Abl融合蛋白引发致癌信号传导。对CML分子基础的了解促使了能够阻断Bcr-Abl酪氨酸激酶活性的高效靶向治疗方法的发展。伊马替尼是目前CML的一线治疗药物,在大多数患者中可诱导持久的治疗反应。然而,患者可能会产生伊马替尼耐药性,这通常是由于BCR-ABL突变所致。随着第二代酪氨酸激酶抑制剂的出现,在伊马替尼治疗失败后,除了干细胞移植外,还有一种有效的治疗选择。随机试验数据表明,在伊马替尼耐药的患者中,达沙替尼治疗优于伊马替尼剂量递增治疗。尼洛替尼是一种最近获批的伊马替尼类似物,在伊马替尼耐药的CML患者中也显示出令人鼓舞的治疗反应。其他药物(包括博舒替尼和INNO-406)正在进行临床开发。随着CML患者可能有多种治疗选择,根据个体患者或疾病特征(例如BCR-ABL突变)量身定制治疗方案或许成为可能。未来CML治疗可能会采用联合策略。总体而言,靶向药物显著改善了被诊断为CML患者的预后。