DRKS00000783已完成3 期
Study of Low-Dose Cytarabine and Etoposide With or Without All-Trans Retinoic Acid in Older Patients Not Eligible for Intensive Chemotherapy With Acute Myeloid Leukemia and NPM1 Mutation - AMLSG 15-10
niversity of Ulm0 个研究点目标入组 144 人开始时间: 2011年4月1日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 144
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 61 Years 至 one(—)
- 性别
- All
入选标准
- •Patients with confirmed diagnosis of acute myeloid leukemia according to the World Health Organization (WHO) classification (including de novo AML, t-AML and s-AML)
- •- Presence of NPM1 mutation as assessed in one of the central AMLSG reference laboratories.
- •- Age > 60 years. There is no upper age limit.
- •- No prior chemotherapy for leukemia except hydroxyurea to control hyperleukocytosis if needed for up to 10 days during the diagnostic screening phase.
- •- Signed written informed consent
- •- Men must give their informed consent that they do not father a baby and must use a latex condom during any sexual contact with women of childbearing potential, even if they have undergone a successful vasectomy. (while on therapy and for 3 month after the last dose of chemotherapy)
- •- WHO performance status = 3
- •- Patients not eligible for intensive chemotherapy according to at least one of the following criteria:
- •- HCT-CI Score >2
- •- Patient's decision
- •- age = 75 years
排除标准
- •- All other AML subtypes, in particular those AML with other recurrent genetic changes (according to WHO 2008):
- •o AML with t(8;21)(q22;q22); RUNX1-RUNX1T1
- •o AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11
- •o AML with t(15;17)(q22;q12); PML-RARA (or other translocations involving RARA)
- •o AML with t(9;11)(p22;q23); MLLT3-MLL (or other translocations involving MLL)
- •o AML with t(6;9)(p23;q34); DEK-NUP214
- •o AML with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1
- •- No consent for registration, storage and processing of the individual disease-characteristics and course as well as information of the family physician and all other treating physicians about study participation
- •- Bleeding disorder independent of leukemia
- •- Uncontrolled infection
- •- Known positive for HIV, HBV or HCV
- •- Organ insufficiency (creatinine >1.5x upper normal serum level; bilirubin, AST or ALP >2.5x upper normal serum level, not attributable to AML; heart failure NYHA III/IV; severe obstructive or restrictive ventilation disorder)
- •- Severe neurological or psychiatric disorder interfering with ability of giving an informed consent
- •- Patients with a currently active second malignancy other than non-melanoma skin cancers. Patients are not considered to have a currently active malignancy if they have completed therapy and are considered by their physician to be at less than 30% risk of relapse within one year.
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