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羟基脲(HU)可有效降低原发性血小板增多症(ET)和真性红细胞增多症(PV)患者外周血中JAK2V617F突变克隆的大小。

Hydroxyurea (HU) is effective in reducing JAK2V617F mutated clone size in the peripheral blood of essential thrombocythemia (ET) and polycythemia vera (PV) patients.

作者信息

Spanoudakis Emmanouil, Bazdiara Ioanna, Kotsianidis Ioannis, Margaritis Dimitrios, Goutzouvelidis Aggelos, Christoforidou Anna, Tsatalas Costas, Bourikas George

机构信息

Department of Haematology, Democritus University of Thrace, Medical School, Area of Dragana, Alexandroupolis, Greece.

出版信息

Ann Hematol. 2009 Jul;88(7):629-32. doi: 10.1007/s00277-008-0650-1. Epub 2008 Dec 19.

DOI:10.1007/s00277-008-0650-1
PMID:19096846
Abstract

Ph-negative chronic myeloproliferative disorders (Ph(neg)cMPD) are treated according to the estimated vascular risk. The recent discovery of V617F point mutation of the JAK2 kinase, which frequently occurs in these diseases, has not changed their management so far. However, emerging data tend to support a prothrombotic role for the mutation, along with a better response of JAK2V617F mutated patients to hydroxyurea treatment. Our data further support this notion.

摘要

Ph 阴性慢性骨髓增殖性疾病(Ph(neg)cMPD)根据估计的血管风险进行治疗。JAK2 激酶 V617F 点突变在这些疾病中频繁出现,但其最近被发现至今尚未改变它们的治疗方式。然而,新出现的数据倾向于支持该突变具有促血栓形成作用,同时 JAK2V617F 突变患者对羟基脲治疗反应更好。我们的数据进一步支持了这一观点。

相似文献

1
Hydroxyurea (HU) is effective in reducing JAK2V617F mutated clone size in the peripheral blood of essential thrombocythemia (ET) and polycythemia vera (PV) patients.羟基脲(HU)可有效降低原发性血小板增多症(ET)和真性红细胞增多症(PV)患者外周血中JAK2V617F突变克隆的大小。
Ann Hematol. 2009 Jul;88(7):629-32. doi: 10.1007/s00277-008-0650-1. Epub 2008 Dec 19.
2
Frequent reduction or absence of detection of the JAK2-mutated clone in JAK2V617F-positive patients within the first years of hydroxyurea therapy.在羟基脲治疗的头几年内,JAK2V617F阳性患者中JAK2突变克隆的检测频率经常降低或未检测到。
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The diagnosis and management of polycythemia vera, essential thrombocythemia, and primary myelofibrosis in the JAK2 V617F era.JAK2 V617F时代真性红细胞增多症、原发性血小板增多症和原发性骨髓纤维化的诊断与管理
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Telomere shortening in Ph-negative chronic myeloproliferative neoplasms: a biological marker of polycythemia vera and myelofibrosis, regardless of hydroxycarbamide therapy.Ph 阴性慢性骨髓增殖性肿瘤中端粒缩短:与羟基脲治疗无关,是真性红细胞增多症和骨髓纤维化的生物学标志物。
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JAK2V617F mutation and hydroxyurea treatment as determinants of immature platelet parameters in essential thrombocythemia and polycythemia vera patients.JAK2V617F 突变和羟基脲治疗对原发性血小板增多症和真性红细胞增多症患者血小板参数的影响。
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Application of PRV-1 mRNA expression level and JAK2V617F mutation for the differentiating between polycytemia vera and secondary erythrocytosis and assessment of treatment by interferon or hydroxyurea.PRV-1 mRNA表达水平和JAK2V617F突变在真性红细胞增多症与继发性红细胞增多症鉴别诊断及干扰素或羟基脲治疗评估中的应用
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Rapid decline of JAK2V617F levels during hydroxyurea treatment in patients with polycythemia vera and essential thrombocythemia.真性红细胞增多症和原发性血小板增多症患者在羟基脲治疗期间JAK2V617F水平迅速下降。
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Interferon α-2b gains high sustained response therapy for advanced essential thrombocythemia and polycythemia vera with JAK2V617F positive mutation.干扰素α-2b对携带JAK2V617F阳性突变的晚期原发性血小板增多症和真性红细胞增多症获得高持续缓解治疗。
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