Tyrolean Cancer Research Center, Internal Medicine V (Hematology and Oncology), Innsbruck Medical University, Innrain 66, Innsbruck, Austria.
Expert Rev Hematol. 2011 Apr;4(2):153-9. doi: 10.1586/ehm.11.9.
Suboptimal response or treatment failure to standard-dose imatinib are relevant problems in chronic-phase chronic myeloid leukemia patients. Insufficient adherence is one of the main causes of insufficient response but biological reasons also have to be considered. Various mechanisms of resistance have been described in the past, some of them mediating absolute resistance and others, relative resistance, to imatinib. The latter can be overcome by dose intensification of imatinib. However, the availability of second-generation tyrosine kinase inhibitors means these patients can be switched to these novel agents. Thus, which strategy is most appropriate for the individual patient with insufficient response to standard-dose imatinib remains elusive. Moreover, it remains unclear whether dose intensification of imatinib in the first-line setting might allow a more rapid and deeper response rate. This article will summarize data on imatinib dose intensification and will make recommendations about which patients imatinib dose intensification is most appropriate for.
标准剂量伊马替尼治疗反应不佳或治疗失败是慢性期慢性髓性白血病患者的相关问题。依从性不足是反应不足的主要原因之一,但也必须考虑到生物学原因。过去已经描述了各种耐药机制,其中一些机制介导对伊马替尼的绝对耐药,而另一些则介导相对耐药。后者可以通过伊马替尼的剂量强化来克服。然而,第二代酪氨酸激酶抑制剂的出现意味着这些患者可以改用这些新型药物。因此,对于标准剂量伊马替尼治疗反应不佳的个体患者,哪种治疗策略最合适仍不明确。此外,在一线治疗中是否增加伊马替尼剂量可能会使缓解率更快、更深,目前尚不清楚。本文将总结伊马替尼剂量强化的数据,并就哪些患者最适合伊马替尼剂量强化提出建议。