医学研究与教育 ›› 2015, Vol. 32 ›› Issue (3): 36-39.DOI: 10.3969/j.issn.1674-490X.2015.03.008

• 临床研究 • 上一篇    下一篇

干扰素α 治疗JAK2V617F 阳性的真性红细胞增多症的疗效观察

郭慧梅,薛华,王静,田明杰,赵雪莲   

  1. 河北大学附属医院血液内科,河北 保定 071000
  • 出版日期:2015-06-25 发布日期:2015-06-25
  • 通讯作者: 田明杰(1980—),女,河北保定人,主管护师,主要从事恶性血液病患者的护理。 E-mail: tianmingjie@foxmail.com
  • 作者简介:郭慧梅(1979—),女,河北邯郸人,主治医师,在读博士,主要从事恶性血液病的研究。E-mail: guohuimei2006@163.com

The efficacy evaluation of interferon alpha on JAK2V617F positive polycythemia vera

GUO Huimei, XUE Hua, WANG Jing, TIAN Mingjie, ZHAO Xuelian   

  1. Department of Hematology, Affiliated Hospital of Hebei University, Baoding 071000, China
  • Online:2015-06-25 Published:2015-06-25

摘要: 目的 分析干扰素α(IFN-α)治疗JAK2V617F 阳性的真性红细胞增多症(PV)的疗效。方法 采用IFN-α 治疗21 例JAK2V617F 阳性的PV 患者,以同期羟基脲(HU)治疗18 例为对照,观察血细胞计数和脾脏变化,并应用荧光定量PCR 方法检测JAK2V617F 表达水平变化,比较两种治疗的血液学和分子学缓解率。结果IFN-α 组血液学总缓解率(CHR+PHR)85.71%,显著高于HU 组(55.56%)。IFN-α 组总分子学缓解率(CMR+PMR)为71.43%,显著高于HU组(5.56%)。结论 相比于HU,IFN-α 可使PV 患者获得更高的血液学缓解率,且可降低JAK2V617F 负荷,达到分子学缓解。

关键词: 真性红细胞增多症, JAK2V617F, 干扰素α

Abstract: Objective To observe the clinical efficacy of interferon alpha(IFN-α) in the treatment of polycythemia vera(PV) patients with JAK2V617F mutation. Methods 21 patients of PV with JAK2V617F mutation were treated with IFN-α, and 18 patients were treated with hydroxyurea(HU) as a control. The changes of blood cell counts and spleen sizes were observed. The expression levels of JAK2V617F were detected by real-time fluorescent quantitative PCR. The hematologic remission rate and molecular remission rate were compared between two groups. Results The overall hematologic remission rate(complete and partial remission) of IFN-α group was 85.71%, which was significantly higher than that of HU group(55.56%). The overall molecular remission rate(complete and partial remission) of IFN-α group was 71.43%, and HU group was 5.56%, the difference was statistically significant. Conclusion Compared with HU, IFN-α not only can make PV patients get a higher hematologic remisson rate, but also can reduce the load of JAK2V617F to reach molecular remisson.

Key words: polycythemia vera, JAK2V617F, interferon alpha

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