Suppr超能文献

高三尖杉酯碱是治疗对羟基脲或干扰素-α治疗无效或不耐受的真性红细胞增多症或原发性血小板增多症患者的有效方法。

Homoharringtonine is an effective therapy for patients with polycythemia vera or essential thrombocythemia who have failed or were intolerant to hydroxycarbamide or interferon-α therapy.

机构信息

Department of Hematology, No. 1 Hospital of Huaian Affiliated to Nanjing Medical University, Huaian, Jiangsu, China,

出版信息

Int J Clin Oncol. 2013 Oct;18(5):922-6. doi: 10.1007/s10147-012-0453-1. Epub 2012 Aug 17.

Abstract

BACKGROUND

At present, the treatment of polycythemia vera (PV) and essential thrombocythemia (ET) is still largely supportive and symptomatic. Homoharringtonine (HHT), a valid drug for treating chronic myelogenous leukemia, has shown some effect on leukemic stem cells. The aim of this study was to observe the effect of HHT on patients with high-risk PV and ET.

METHODS

Patients with high-risk PV (n = 17) or ET (n = 18) who had failed or were intolerant to hydroxycarbamide or interferon-α therapy received HHT at a dose of 1.5 mg/m(2) daily by continuous infusion for 7 days every month. Hematological responses were evaluated at the 6th month after HHT therapy.

RESULTS

After six courses of HHT therapy, the hematological response rates were 64.7 % (11/17) in PV and 72.2% (13/18) in ET. In PV, the single sign remission rates of constitutional symptoms, symptomatic splenomegaly, pruritus and bone pain were 70.0% (7/10), 77.8% (7/9), 50% (1/2) and 100% (3/3), respectively. The remission rates of constitutional symptoms and symptomatic splenomegaly in ET were 66.7% (6/9) and 71.4% (5/7), respectively. The rates of grade 1 granulocytopenia and thrombocytopenia were 1.8 and 0.9%, respectively. No grade 2 or over events, or pancytopenia were observed.

CONCLUSIONS

Low-dose HHT alone has considerable short-term efficacy for high-risk PV/ET and may used as a second-line drug for PV/ET treatment in patients who have failed or were intolerant to hydroxycarbamide or interferon-α therapy.

摘要

背景

目前,真性红细胞增多症(PV)和原发性血小板增多症(ET)的治疗仍主要是支持和对症治疗。高三尖杉酯碱(HHT)是一种治疗慢性髓性白血病的有效药物,对白血病干细胞有一定疗效。本研究旨在观察 HHT 对高危 PV 和 ET 患者的疗效。

方法

17 例高危 PV 和 18 例 ET 患者在羟基脲或干扰素-α治疗失败或不耐受后,采用 HHT 治疗,剂量为 1.5mg/m²,每日持续输注,每月 7 天。在 HHT 治疗后 6 个月评估血液学反应。

结果

在 6 个疗程的 HHT 治疗后,PV 的血液学反应率为 64.7%(11/17),ET 为 72.2%(13/18)。在 PV 中,单一症状缓解率分别为全身症状、有症状的脾肿大、瘙痒和骨痛的 70.0%(7/10)、77.8%(7/9)、50%(1/2)和 100%(3/3)。ET 中全身症状和有症状的脾肿大的缓解率分别为 66.7%(6/9)和 71.4%(5/7)。1-2 级粒细胞减少和血小板减少的发生率分别为 1.8%和 0.9%。未观察到 2 级或更高级别的事件或全血细胞减少。

结论

低剂量 HHT 单独使用对高危 PV/ET 有相当短期的疗效,可作为羟基脲或干扰素-α治疗失败或不耐受的 PV/ET 患者的二线治疗药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验