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临床试验/NCT00995332
NCT00995332已完成1 期

Treatment of Acute Myelogenous Leukemia With the Histone Deacetylase Inhibitor Valproic Cid in Combination With All-trans Retinoic Acid (ATRA) and Low Dose Cytarabine

University of Bergen1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2009年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
36
试验地点
1
主要终点
Survival

研究概览

简要总结

Hypothesis: Combined treatment with valproic acid and ATRA can be used to achieve disease stabilization for a subset of patients with acute myelogenous leukemia (AML), and this effect can be improved without serious toxicity by adding low-dose cytarabine to this treatment.

Adult patients >18 years of age who can be included:

Elderly patients who cannot achieve standard chemotherapy, patients with relapsed or resistant AML.

Treatment: Combined therapy with:

Valproic acid, continuous therapy until disease progression ATRA, oral therapy for 14 days every three months Low-dose cytarabine 10 mg/m2 up to 10 injections during week 2 and 3, repeated every 3 months.

详细描述

Patients to be included:

  1. Elderly patients (>60 years of age) or other patients unfit for conventional intensive chemotherapy with newly diagnosed acute myelogenous leukemia (AML).
  2. Adult patients of any age (>18 years of age) with relapsed or resistant AML who cannot receive conventional therapy.

Treatment:

Valproic acid to be started on day 1 as continuous therapy until disease progression.

ATRA administered from day 8 orally as 22.5 mg/m2 twice daily for 14 days, repeated every third month.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Recently diagnosed AML in patients unfit for intensive chemotherapy
  • Patients with relapsed or refractory AML

排除标准

  • No informed consent
  • Intolerance to study drugs
  • Serious liver disease

研究组 & 干预措施

ATRA+valproc acid+low-dose cytarabine

Experimental

干预措施: Cytarabine, all-trans retinoic acid, valproic acid (Drug)

结局指标

主要结局

Survival

时间窗: 3 years

次要结局

  • Disease complications(3 years)
  • Disease stabilization(3 years)
  • Side effects of therapy(3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Øystein Bruserud

Professor

University of Bergen

研究点 (1)

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