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临床试验/DRKS00000783
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.

研究者

发起方
niversity of Ulm

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