Second-line Therapy and Beyond Resistance for the Treatment of Patients With Chronic Myeloid Leukemia Post Imatinib Failure

Elias Jabbour, Jorge E. Cortés, Hagop Kantarjian
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引用次数: 12

Abstract

Chronic myeloid leukemia (CML) is characterized at the molecular level by the presence of the Philadelphia chromosome (Ph) and the resultant oncogenic signaling by the BCR-ABL fusion protein. The treatment and outlook for CML were revolutionized by the introduction of imatinib, but resistance is a substantial barrier to successful treatment in many patients. Introduction of the second-generation tyrosine kinase inhibitors (TKI) dasatinib and nilotinib has provided effective therapeutic options for many patients with resistance to front-line imatinib. However, the T315I mutation remains a significant clinical issue because it is insensitive to all currently available agents. A number of new agents are in development and many hold the promise of activity in T315I-mutated disease. Successful treatment of patients with disease harboring T315I might lie in the effective combination or sequencing of these new agents with existing TKI therapies.

伊马替尼治疗失败后慢性髓系白血病患者的二线治疗和超耐药
慢性髓性白血病(CML)在分子水平上的特征是费城染色体(Ph)的存在和由此产生的BCR-ABL融合蛋白的致癌信号传导。伊马替尼的引入彻底改变了CML的治疗和前景,但耐药性是许多患者成功治疗的实质性障碍。第二代酪氨酸激酶抑制剂(TKI)达沙替尼和尼洛替尼的引入为许多对一线伊马替尼耐药的患者提供了有效的治疗选择。然而,T315I突变仍然是一个重要的临床问题,因为它对目前所有可用的药物都不敏感。许多新药物正在开发中,其中许多有望在t315i突变疾病中发挥作用。携带T315I的疾病患者的成功治疗可能取决于这些新药与现有TKI疗法的有效组合或排序。
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