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临床试验/NCT02427919
NCT02427919Unknown2 期

The DEtection of G-CSF REceptor With Flow Cytometry and Identification of the Effect of G-CSF After Salvage Chemotherapy in Relapsed or Refractory AML

Seoul St. Mary's Hospital1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2015年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
56
试验地点
1
主要终点
Recovery time from neutropenia

研究概览

简要总结

Granulocyte Colony Stimulating Factor (G-CSF, filgrastim) is now widely used after chemotherapy which complicates hematological toxicity involving neutropenia. As prolonged neutropenia leads to neutropenic fever due to bacteremia or fungal infection, the use of G-CSF prevents severe infectious complication in various cancer patients.

In acute myeloid leukemia (AML), leukemic blasts have been expected to have G-CSF receptor which may be stimulated by G-CSF, and refractory patients were not treated with G-CSF in salvage chemotherapy in Catholic blood and marrow transplantation (BMT) Center for a long time. This strategy induced prolonged neutropenia and a lot of infectious complications some of which led to deaths.

Although there are some data which remind us G-CSF may proliferate leukemic blasts, the investigators also identified several reports which suggested that subgroup with G-CSF use showed acceptable CR rate and improved survival outcomes compared to a subgroup without G-CSF use.

Therefore investigators are now trying to identify the effects of G-CSF for refractory AML patients in salvage chemotherapy setting regarding the duration of neutropenia and admission, incidence of infectious complications and the duration of antibiotics application. Furthermore, overall response rate (CR+CRi) after salvage chemotherapy and survival outcomes will be calculated according to G-CSF use.

Also, investigators will detect G-CSF receptor using cluster of differentiation 114 (CD114), and analyze the clinical outcomes according to the subgroups with or without using G-CSF during neutropenic period.

详细描述

Patients will be treated with mitoxantrone and etoposide and cytarabine. Patients will be randomly divided according to the usage of G-CSF.

Subgroup with G-CSF will be treated with G-CSF after 7~10 days post-chemotherapy, when blasts will disappear from peripheral blood.

Subgroup without G-CSF will be observed until 25~28 days post-chemotherapy. If blood counts are nor recovered, the investigators can perform bone marrow biopsy to identify the status of the bone marrow.

After then, G-CSF can be applied if blasts are not observed in both peripheral blood and bone marrow.

When absolute neutrophil counts are recovered and there are no evidence of infectious complications, patients will discharge safely from hospital.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
17 Years 至 64 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Eastern Cooperative Oncology Group (ECOG) performance status 0~2
  • AML with remission failure after standard chemotherapy
  • Stable liver and renal function (=< Upper normal limit (UNL) x 2.5)
  • Stable heart and lung function (Ejection Fraction (EF) > 45%, Forced expiratory volume at one second (FEV1) > 40%)

排除标准

  • Acute promyelocytic leukemia
  • Central nervous system (CNS) involvement
  • Uncontrolled bleeding
  • Uncontrolled infectious complication
  • Pregnancy, Breast feeding
  • Significant cardiovascular disease within 6 months
  • Significant organ failure (> UNL x 2.5)

研究组 & 干预措施

Early G-CSF use

Experimental

Refractory AML undergoing salvage chemotherapy (MEC regimen in AML). After finishing application of chemotherapy, G-CSF will be started post chemotherapy D+7~D+10 when blasts disappear from peripheral blood smear.

When blasts reappear on peripheral blood smear, G-CSF will be discontinued.

Intervention type : Drug Intervention name : G-CSF (Filgrastim)

-> Comparison of the effect of G-CSF (Filgrastim) use

干预措施: G-CSF (Drug)

No or delayed G-CSF use

Active Comparator

Refractory AML undergoing salvage chemotherapy (MEC regimen in AML). After finishing application of chemotherapy, G-CSF will not be applied at least post chemotherapy D+25~D+28. If patient suffers from severe infectious complication and when no blasts are detected on peripheral blood smear, G-CSF can be started then.

Intervention type : Drug Intervention name : G-CSF (Filgrastim)

-> Comparison of the effect of G-CSF (Filgrastim) use

干预措施: G-CSF (Drug)

结局指标

主要结局

Recovery time from neutropenia

时间窗: 30 days

次要结局

  • Incidence of neutropenic fever and infectious complication(30 days)
  • Overall survival(3 year)
  • Complete remission rate(45 days)
  • Disease free survival(3 year)

研究者

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

Jae-Ho, Yoon

Clinical assistant professor

Seoul St. Mary's Hospital

研究点 (1)

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