Thomas Xavier
Hématologie, Hôpital Edouard-Herriot, 5, place d'Arsonval, 69437 Lyon.
Bull Cancer. 2007 Oct;94(10):871-80.
Distinct clinicopathologic acute lymphoblastic leukemia (ALL) entities have been identified, resulting in the adoption of risk-oriented treatment approaches. In Philadelphia chromosome-positive ALL, the optimal treatment requires the addition of BCR-ABL tyrosine kinase inhibitors, as imatinib. Despite advances, the outcome remains poor, and novel agents are desperately required. The emergence of resistance to the Bcr-Abl inhibitor imatinib mesylate in patients with Philadelphia chromosome-positive (Ph+) ALL has prompted the development of second-generation compounds active against mutant forms, including dasatinib and nilotinib.
已确定了不同的临床病理急性淋巴细胞白血病(ALL)实体,从而采用了以风险为导向的治疗方法。在费城染色体阳性ALL中,最佳治疗需要添加BCR-ABL酪氨酸激酶抑制剂,如伊马替尼。尽管取得了进展,但结果仍然很差,迫切需要新型药物。费城染色体阳性(Ph+)ALL患者对Bcr-Abl抑制剂甲磺酸伊马替尼产生耐药性,促使开发对突变形式有活性的第二代化合物,包括达沙替尼和尼洛替尼。