EUCTR2007-003514-34-FR进行中(未招募)1 期
A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete Remission - HCT versus CT elderly AM
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- EBMT
- 入组人数
- 218
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Age > or équal 60years and < ou equal 75 years
- •- AML as defined by WHO
- •- Refractory anemia with excess of blasts (RAEB)
- •- primary and secondary AML
- •- First complete remission following one or two cycles of induction chemotherapy, according to current participating cooperative group protocols
- •- Presence of an HLA-identical familiy donor or an unrelated donor (6/6 or 10/10 according to the center policy)
- •- a male donor is preferred for male recipients
- •- Karnofsky score > 70 (see appendix D)
- •- Written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- AML FAB M3
- •- Patients aged > 70 years with a comorbidity score =2 according to the modified charlson comobidity index (Sorror score –see Appendix)
- •- Organ dysfunction
- •- Patients with creatinine clearance < 50 ml/min
- •- Cardiac ejection fraction < 50%
- •- Severe defects in pulmonary function testing (defects are currently categorized as mild, moderate and severe) as defined by the pulmonary consultant, or receiving supplementary continuous oxygen
- •- Liver function tests: total bilirubin > 2x the upper limit of normal, SGOT and SGPT - 4x the upper limit of normal
- •- Karnofsky score £ 60 (see appendix D )
- •- Patients with poorly controlled hypertension
- •- HIV positivity
- •- Treament in other clinical studies with investigational drugs
- •- Exclusion criteria apply at time of randomization
研究者
相似试验
进行中(未招募)
1 期
A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete RemissioAcute Myeloid LeukaemiaMedDRA version: 14.1Level: PTClassification code 10000881Term: Acute myeloid leukaemia (in remission)System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)EUCTR2007-003514-34-NLEuropean Group for Blood and Marrow trasnplantation231
已完成
3 期
A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete Remission.10024324Acute myeloid leukemialeukemiaNL-OMON39855European Group for Blood and Marrow Transplantation60
进行中(未招募)
1 期
A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete Remission. - HCT vs. CT elderly AMAcute Myeloid LeukaemiaMedDRA version: 20.0Level: PTClassification code 10000881Term: Acute myeloid leukaemia (in remission)System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)EUCTR2007-003514-34-DEEuropean Society for Blood and Marrow Transplantation EBMT231
进行中(未招募)
1 期
A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete Remission.EUCTR2007-003514-34-ATEuropean Group for Blood and Marrow Transplantation231
进行中(未招募)
1 期
A Randomized Phase III Study Comparing Conventional Dose Treatment Using a Combination of Lenalidomide, Bortezomib and Dexamethasone (RVD) to High-Dose Treatment with Peripheral Stem Cell Transplant in the Initial Management of Myeloma in Patients up to 65 Years of Age (IFM/DFCI 2009) - IFM/DFCI 2009EUCTR2009-016871-32-FRCHU de TOULOUSE1,000
