Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Natl Compr Canc Netw. 2012 Oct 1;10 Suppl 3:S1-S13. doi: 10.6004/jnccn.2012.0184.
Despite the success with tyrosine kinase inhibitors (TKIs) in most patients with chronic myelogenous leukemia (CML), some patients still experience resistance or intolerance and need alternative therapies. Monitoring response to TKI therapy is a critical component of managing CML, and molecular response seems to be the most important milestone for predicting long-term outcomes. How best to assess response, including how to define treatment failure, and how monitoring should be conducted remain controversial. Strategies for overcoming imatinib resistance include increasing the imatinib dose or switching to a second-generation TKI. Another approach is to use higher doses of imatinib or second-generation TKIs up front to increase the rate of earlier responses, with the hope that this will translate into a reduced risk of resistance. Several investigational therapies are also being evaluated as a means of overcoming TKI resistance, including ponatinib (AP24534), omacetaxine, and bosutinib (SKI-606). Allogeneic hematopoietic stem cell transplantation has also shown efficacy in patients with imatinib-resistant disease. Alternatives to long-term TKI therapy that are currently being explored include discontinuation of treatment and eradication of minimal residual disease with investigational treatment regimens, such as those involving interferon, hydroxychloroquine, BCL6 inhibitors, and the smoothened antagonists LDF225 and BMS-833923.
尽管酪氨酸激酶抑制剂 (TKI) 在大多数慢性髓性白血病 (CML) 患者中取得了成功,但仍有一些患者出现耐药或不耐受,需要替代疗法。监测 TKI 治疗的反应是管理 CML 的关键组成部分,分子反应似乎是预测长期结果的最重要里程碑。如何最好地评估反应,包括如何定义治疗失败以及如何进行监测仍存在争议。克服伊马替尼耐药的策略包括增加伊马替尼剂量或改用第二代 TKI。另一种方法是在开始时使用更高剂量的伊马替尼或第二代 TKI,以提高早期反应率,希望这将转化为降低耐药风险。几种研究性疗法也被评估为克服 TKI 耐药的方法,包括 ponatinib (AP24534)、omacetaxine 和 bosutinib (SKI-606)。同种异体造血干细胞移植在伊马替尼耐药疾病患者中也显示出疗效。目前正在探索的替代长期 TKI 治疗的方法包括停止治疗和用研究性治疗方案消除微小残留疾病,例如涉及干扰素、羟氯喹、BCL6 抑制剂以及 smoothened 拮抗剂 LDF225 和 BMS-833923 的方案。