跳至主要内容
临床试验/NCT01004965
NCT01004965已完成不适用

Multidrug Resistance Studies in Acute Myeloid Leukemia

Alliance for Clinical Trials in Oncology46 个研究点 分布在 1 个国家目标入组 2,034 人开始时间: 1997年3月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
2,034
试验地点
46
主要终点
completion rate

研究概览

简要总结

This research study is looking at bone marrow and blood samples in patients with untreated acute myeloid leukemia or acute lymphoblastic leukemia enrolled on clinical trial CALGB-9621, CALGB-9720, CALGB 19808, and CALGB 10201. Studying samples of bone marrow and blood from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment.

详细描述

OBJECTIVES:

I. Determine Pgp antigen expression and Pgp-mediated functional multidrug resistance (MDR) in pretreatment acute myeloid leukemia (AML) cells from adult patients enrolled on CALGB clinical trials of PSC-833 Pgp modulation.

II. Correlate Pgp-mediated MDR with patient pretreatment characteristics including age, immunophenotype, and karyotype.

III. Correlate Pgp expression, function, and in vitro modulation by PSC-833 with treatment outcome in previously untreated AML patients treated on CALGB Pgp modulation trials.

IV. Determine Pgp expression and function in AML cells from patients with refractory or relapsed leukemia following induction chemotherapy administered with or without PSC-833.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Previously untreated patients eligible for and registered to a CALGB multidrug resistance modulation treatment protocol for acute myeloid leukemia (CALGB 9621, CALGB-9720, CALGB-19808, and CALGB 10201) OR protocols for previously untreated acute lymphocytic leukemia
  • Performance status: not specified

排除标准

  • 未提供

结局指标

主要结局

completion rate

时间窗: Up to 5 years

次要结局

  • duration of completion rate(Up to 5 years)
  • survival(Up to 5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (46)

Loading locations...

相似试验