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临床试验/NCT00129155
NCT00129155Unknown2 期

Unrelated Reduced Intensity Conditioning With Treosulfan® for Allogeneic Stem Cell Transplantation in Patients With Hematological Malignancies

Hospices Civils de Lyon2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2005年2月最近更新:
适应症
相关药物

试验速览

阶段
2 期
入组人数
30
试验地点
2
主要终点
Overall survival at 1 year

研究概览

简要总结

In this study, treosulfan is evaluated for conditioning in allogenic stem cell transplantation. The procedure and the follow-up are the same as in standard allogenic transplant.

The donor is unrelated (identical HLA). The graft is haematological peripheral blood stem cell.

The conditioning with reduced intensity is: fludarabine (from day -6 to day -2), treosulfan (from day -6 to day -4) and thymoglobuline (from day -2 to day -1).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • AGE: >= 18 years and <= 65 years
  • Patients with a too high transplant-related mortality (TRM) after standard transplantation (multiple myeloma, chronic lymphoid leukemia, non Hodgkin's lymphoma, myelodysplasia)
  • Patients with visceral contra-indication for standard transplantation:
  • cardiac: myocardiopathy; forced expiratory volume (FEV) < 50%;
  • respiratory: abnormal carbon monoxide diffusing capacity (DLCO);
  • renal: creatinine clearance < 50ml/min;
  • hepatic: transaminases and bilirubin > 2 upper normal limit;
  • infectious: controlled fungal infection.
  • Karnofsky score >= 70%
  • Unrelated donor HLA identical (ABC, DRB1; DQB1)
  • Signed informed consent
  • Diagnosis :
  • Chronic myelogenous leukemia (CML):
  • In first chronic phase, resistant to interferon with or without aracytine or refractory or resistant to Glivec
  • In complete response (CR) or in 2nd partial response (PR) after being in blastic phase
  • Multiple myeloma (MM):
  • Relapse after autograft if the therapeutic response was evaluated to 50%
  • Non-Hodgkin's lymphoma (NHL):
  • Mantle cell lymphoma after first relapse but in case of chemosensitivity ≥ 50% except for high grade lymphoma
  • In 2nd CR or PR chemosensitive in response ≥ 50% after autograft
  • Chronic lymphocytic leukemia (CLL):
  • In 2nd CR or PR or in response ≥ 50% after autograft or in 2nd relapse after 2 lines of treatment but in case of chemosensitivity ≥ 50%
  • Acute myeloid leukemia (AML):
  • In 2nd CR or in 1st CR for high risk criteria [high risk criteria defined by: LAM 7; leukocytes > 30,000/mm3; chromosomal abnormalities: t(6,9); abnormalities of 11q23, 17p, 11q, 20q, 21q, -5, del(5q), -7/del7q, del 9q et inv 3q]
  • Acute lymphoblastic leukemia (ALL):
  • In 2nd CR or in 1st CR if high risk criteria patients who are defined by chromosomal abnormalities t(9,22); t(1,19); t(4,11); abnormalities of 11q23
  • Myelodysplastic syndromes (MDS):
  • Patients without prior chemotherapy, with intermediate or high International Prognostic Scoring System (IPSS) score and blast cells < 1% in bone marrow (BM)
  • CR or PR after chemotherapy for patients with 20 to 30% of blast cells in BM
  • Secondary AML patients with a response to chemotherapy (< 30% blasts in BM and < 5% of blast cells in blood)
  • Adequate contraception in female patients of child bearing potential

排除标准

  • 未提供

结局指标

主要结局

Overall survival at 1 year

次要结局

  • Acute and chronic graft-versus-host disease incidence and severity
  • Evaluation of conditioning and transplant toxicity
  • Chimerism evaluation
  • Response rate and survival without progression
  • Engraftment evaluation

研究者

申办方类型
Other

研究点 (2)

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