Thomas Xavier
Hôpital Édouard-Herriot, Hématologie, 5, place d’Arsonval, 69437 Lyon, France.
Bull Cancer. 2011 Jul;98(7):761-7. doi: 10.1684/bdc.2011.1390.
Distinct clinicopathologic acute lymphoblastic leukemia (ALL) entities have been identified, resulting in the adoption of risk-oriented treatment approaches. In Philadelphia chromosome-positive (Ph(+)) ALL, the optimal treatment requires the addition of BCR-ABL tyrosine kinase inhibitors, as imatinib. However, the outcome remains poor in absence of allogeneic stem cell transplantation, and novel agents are desperately required. Resistance attributable to kinase domain mutations can lead to relapse despite the development of second-generation compounds, including dasatinib and nilotinib. Despite these therapeutic options, the cross-resistant BCR-ABL (T315I) mutation remains a major clinical challenge. The first evaluations of AP24534 present this drug as a potent multi-targeted kinase inhibitor active against T315I and all other BCR-ABL mutants. AP24534 could be the next treatment of choice in hematological malignancies with Philadelphia-positive chromosome, particularly Ph(+) ALL known for its frequent occurrence of T315I mutation.
已确定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(Ph(+))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。然而,在没有异基因干细胞移植的情况下,预后仍然很差,迫切需要新型药物。尽管开发了第二代化合物,包括达沙替尼和尼洛替尼,但激酶结构域突变导致的耐药性仍可导致复发。尽管有这些治疗选择,交叉耐药的BCR-ABL(T315I)突变仍然是一个主要的临床挑战。对AP24534的首次评估表明,该药物是一种有效的多靶点激酶抑制剂,对T315I和所有其他BCR-ABL突变体均有活性。AP24534可能成为费城染色体阳性血液系统恶性肿瘤的下一个治疗选择,尤其是以频繁发生T315I突变而闻名的Ph(+) ALL。