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选择对伊马替尼耐药的慢性髓性白血病患者的最佳治疗策略:权衡具有 BCR-ABL 突变和患者病史的个体药物的疗效和安全性。

Choosing the best treatment strategy for chronic myeloid leukemia patients resistant to imatinib: weighing the efficacy and safety of individual drugs with BCR-ABL mutations and patient history.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 423, Houston, TX 77030, USA.

出版信息

Leukemia. 2010 Jan;24(1):6-12. doi: 10.1038/leu.2009.193. Epub 2009 Oct 1.

DOI:10.1038/leu.2009.193
PMID:19798095
Abstract

For patients with chronic myeloid leukemia who become or are inherently resistant to imatinib therapy, including dose escalation, several important factors must be considered when deciding which strategy to attempt next. The second-generation tyrosine kinase inhibitors (TKIs) dasatinib and nilotinib offer improved potency and a high likelihood of success for these patients. Overall, the efficacy data are comparable for these two agents, and so physicians should consider the BCR-ABL mutation profile and the patient's history to make an educated decision on the best choice. Only a few BCR-ABL mutations seem to be less responsive to either nilotinib or dasatinib and it is recommended to choose the second-line TKI that has shown clinical activity against the specific mutation in these cases. For patients with all other mutations, and for patients with no mutations, it is recommended to choose the second-generation TKI based on the patient's disease history. It is important to choose an agent that minimizes the likelihood of exacerbating the patient's past tolerability issues to imatinib, or comorbid conditions. Here, we propose a treatment algorithm for imatinib-resistant patients based on BCR-ABL mutation status and patient history.

摘要

对于那些对伊马替尼治疗产生或固有耐药的慢性髓性白血病患者,包括剂量升级,在决定下一步尝试哪种策略时,必须考虑几个重要因素。第二代酪氨酸激酶抑制剂(TKI)达沙替尼和尼洛替尼为这些患者提供了更高的疗效和成功率。总的来说,这两种药物的疗效数据相当,因此医生应考虑 BCR-ABL 突变谱和患者的病史,以便就最佳选择做出明智的决策。只有少数 BCR-ABL 突变似乎对尼洛替尼或达沙替尼的反应性较低,建议在这些情况下选择对特定突变具有临床活性的二线 TKI。对于其他所有突变的患者和无突变的患者,建议根据患者的疾病史选择第二代 TKI。选择一种能够最大程度减少加重患者既往对伊马替尼不耐受问题或合并症的可能性的药物非常重要。在这里,我们根据 BCR-ABL 突变状态和患者病史提出了一种针对伊马替尼耐药患者的治疗算法。

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