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一名处于加速期骨髓增殖性疾病且血小板衍生生长因子受体β基因重排的患者对甲磺酸伊马替尼无反应。

Lack of response to imatinib mesylate in a patient with accelerated phase myeloproliferative disorder with rearrangement of the platelet-derived growth factor receptor beta-gene.

作者信息

Bastie Jean-Noël, Garcia Isabel, Terré Christine, Cross Nicholas C P, Mahon Francois-Xavier, Castaigne Sylvie

出版信息

Haematologica. 2004 Oct;89(10):1263-4.

Abstract

Imatinib mesylate has been reported to produce positive results in atypical chronic myeloproliferative disorders (CMD) with chromosomal translocations that disrupt the platelet-derived growth factor receptor beta gene (PDGFRB). We used imatinib to treat a 49-year old man with atypical CMD in accelerated phase and the H4 (D10S170)-PDGFRB fusion gene. After 3 months of treatment, we observed grade 4 hematologic toxicity and a lack of response.

摘要

据报道,甲磺酸伊马替尼对伴有染色体易位且破坏血小板衍生生长因子受体β基因(PDGFRB)的非典型慢性骨髓增殖性疾病(CMD)产生了积极疗效。我们使用伊马替尼治疗一名49岁处于加速期且携带H4(D10S170)-PDGFRB融合基因的非典型CMD男性患者。治疗3个月后,我们观察到4级血液学毒性且无反应。

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