首页> 外文期刊>Bulletin du Cancer: Journal de l'Association Francaise pour l'Etude du Cancer >Is AP24534 (Ponatinib) the next treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia?
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Is AP24534 (Ponatinib) the next treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia?

机译:AP24534 (Ponatinib)下一个治疗费城染色体阳性急性淋巴细胞白血病吗?

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摘要

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.
机译:不同临床病理的急性淋巴细胞白血病(ALL)实体已确定,导致采用风险导向治疗方法。染色体阳性(Ph值(+)),最优治疗需要bcr - abl的加法酪氨酸激酶抑制剂,如伊马替尼。结果在没有同种异体仍然贫困干细胞移植,小说代理迫切需要。激酶结构域突变可导致复发尽管第二代的发展化合物,包括达沙替尼和nilotinib。尽管这些治疗选项,cross-resistant bcr - abl (T315I)突变一个主要的临床挑战。AP24534现在的这种药物作为强有力的多靶向激酶抑制剂活性T315I和所有其他bcr - abl突变体。可能是下一个治疗的选择血液恶性肿瘤与费城阳性染色体,尤其是Ph值(+)所有已知的频繁发生T315I mutation。

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