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伊马替尼与阿那格雷联合治疗急变期慢性髓性白血病

[Combination of imatinib and anagrelide in treatment of chronic myeloid leukemia in blastic phase].

作者信息

Voglová J, Maisnar V, Beránek M, Chrobák L

机构信息

Oddelení klinické hematologie II. interní kliniky Lékarské fakulty UK a FN Hradec Králové.

出版信息

Vnitr Lek. 2006 Sep;52(9):819-22.

PMID:17091608
Abstract

Chronic myeloid leukemia in blast phase (BP) is resistant to chemotherapy and majority of patients die within 6 months. Inhibitor Bcr-Abl tyrosine kinase imatinib mesylate dramatically improved outcome of patients in chronic phase (CP) and is also effective in BP of CML. The prognosis of patients treated with imatinib in BP is worse than in CP. High platelet counts are often observed at diagnosis or in the subsequent course of the CML in about 25% of patients. Thrombohemorrhagic complications associated with the thrombocythemia may be serious. Anagrelide selectively reduces circulating platelets and is used in treatment of thrombocythemia in chronic myeloproliferative disorders. Efficacy and safety of combination imatinib mesylate with anagrelide was demonstrated in chronic and accelerated phase of CML. No study about the use of imatinib with anagrelide in BP has been found. 51-year-old white man with CML presented in blast phase was followed for 4 years. Imatinib mesylate in dose of 600 mg p.o. qd. was administered after the failure of initial chemotherapy. The patient was treated with imatinib for 45 months, 14.5 months in combination with anagrelide. Partial hematologic response in duration of 33 months was induced by imatinib, cytogenetic response was not reached. Imatinib-resistant thrombocythemia was controlled with anagrelide in dose of 0.5-1 mg p.o. qd. No thrombohemorrhagic complications were observed. The patient tolerated the combination of imatinib and anagrelide well and long-term survival gave him the chance of treatment with the new tyrosin kinase inhibitor (dasatinib).

摘要

急变期慢性髓性白血病(BP)对化疗耐药,大多数患者在6个月内死亡。Bcr-Abl酪氨酸激酶抑制剂甲磺酸伊马替尼显著改善了慢性期(CP)患者的预后,对慢性髓性白血病的急变期也有效。伊马替尼治疗急变期患者的预后比慢性期差。在约25%的慢性髓性白血病患者诊断时或后续病程中常观察到血小板计数升高。与血小板增多相关的血栓出血并发症可能很严重。阿那格雷可选择性减少循环血小板,用于治疗慢性骨髓增殖性疾病中的血小板增多症。甲磺酸伊马替尼与阿那格雷联合应用在慢性髓性白血病慢性期和加速期的疗效和安全性已得到证实。尚未发现有关伊马替尼与阿那格雷在急变期联合应用的研究。一名51岁处于急变期的慢性髓性白血病白人男性患者接受了4年随访。初始化疗失败后给予口服甲磺酸伊马替尼600 mg,每日1次。该患者接受伊马替尼治疗45个月,其中14.5个月与阿那格雷联合应用。伊马替尼诱导了持续33个月的部分血液学缓解,但未达到细胞遗传学缓解。伊马替尼耐药的血小板增多症通过口服阿那格雷0.5 - 1 mg,每日1次得到控制。未观察到血栓出血并发症。患者对伊马替尼和阿那格雷的联合治疗耐受性良好,长期生存使他有机会接受新型酪氨酸激酶抑制剂(达沙替尼)治疗。

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