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临床试验/NCT04296214
NCT04296214撤回不适用

Pharmacoeconomics in the Application of 5-azacitidine in the Treatment of Myelodysplastic Syndromes and Acute Myeloid Leukemia

Grupo Cooperativo de Hemopatías Malignas1 个研究点 分布在 1 个国家开始时间: 2020年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
1
主要终点
Response Rate

研究概览

简要总结

The investigators want to compare the global response rate of patients with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) after six months of treatment with 5-azacitidine on two different doses. First group of 50 mg/m2 for 10 days each 28 days versus 75 mg/m2 for 7 days on 28 days cycles.

详细描述

5-Azacitidine it's the standard treatment for patients with MDS and it is widely used for AML in patients that aren't fit for intensive treatment. The standard dose of azacitidine is 75 mg/m2 for 7 días on 28 days cycles. Nevertheless there are studies of pharmacokinetics that have showed there is no difference on plasmatic distribution between 25, 50, 75 or 100 mg/m2 with similar concentration curves. The actual presentation of azacitidine is 100 mg per bottle with less of 24 hours of utility after opened. Looking for optimizations on the use of 5-azacitidine, we have changed the dosing to 50 mg/m2 for 10 days on 28 days cycles with a total dose application of 95% of the traditional regimen with the saving of 5 bottles of the drug.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

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

  • Age ≥18 years
  • Confirmed diagnosis of MDS that require treatment with 5-aza characterized by: i) RAEB-1 defined as the presence of 5%-9% of myeloblasts in bone marrow; ii) RAEB-2 defined as the presence of 10%-19% of myeloblasts in bone marrow or 5%-19% blasts in peripheral blood; iii) IPSS-R very high, high or intermediate
  • Confirmed AML with blasts ≥ 20% in bone marrow or peripheral blood and that its not candidate to receive intense chemotherapy at consideration of the physician.
  • Performance status of 0, 1 o 2 by the Eastern Cooperative Oncology Group (ECOG).
  • Availability to sign an informed consent

排除标准

  • Previous treatment for MDS or AML with chemotherapy or another antineoplastics including hypomethylating agents.
  • Acute promyelocytic leukemia

研究组 & 干预措施

A

Azacitidine 50 mg/m2 for 10 days each 28 days

干预措施: 5-azacitidine (Drug)

B

Azacitidine 75 mg/m2 for 7 days each 28 days

干预措施: 5-azacitidine (Drug)

结局指标

主要结局

Response Rate

时间窗: 6 months

Global response rate by International Criteria

次要结局

未报告次要终点

研究者

发起方
Grupo Cooperativo de Hemopatías Malignas
申办方类型
Other
责任方
Sponsor

研究点 (1)

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