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临床试验/NCT01873807
NCT01873807Unknown4 期

An Open-label,Multi-center,Prospective Study of Idarubicin and Etoposide Intensified Conditioning Regimen Allogeneic Hematopoietic Stem Cell Transplantation for Adult Acute Lymphoblastic Leukemia

Nanfang Hospital, Southern Medical University13 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2013年5月最近更新:
适应症
干预措施

试验速览

阶段
4 期
入组人数
100
试验地点
13
主要终点
Event-Free Survival

研究概览

简要总结

Intensified conditioning regimen allo-HSCT is based on a hypothesis of that intensifying condition with less-used drugs could overcome resistance,reduce tumor burden, and most importantly, spare enough time for slow-growing GVL effect following immune reconstitution to finally get rid of MRD and control the disease. Our previous trial of HDE-ALL-2011 (NCT01457040) have confirmed the role of intensified conditioning allo-HSCT in adult ALL, resulting in significantly improved OS and EFS in comparison with previous standard TBI/CY2 conditioning regimen(data not yet published). But at the same time, FA-TBI/CY2-VP16 conditioning regimen was associated with high transplantation-related mortality (TRM), which might be attributed to excessive suppression on both bone marrow and immune. TT-ALL-HIE-2013, substituting FA with idarubicin, is aimed at maintaining anti-tumor effect with less cross-resistance and immune suppression and reducing TRM.

详细描述

It's well-known that the long-term outcome of adult acute lymphoblastic leukemia (ALL) lags far behind that of pediatric ALL,associated with different molecular cytogenetics make-up and treatment strategies. In search of an optimal regimen for pediatric ALL, comprehensive series of clinical trials of intensive chemotherapies have been conducted and lead to 80%-90% long-term survival. At the same time, pediatric-inspired chemotherapy protocol aslo yielded a charming result of 50-60% 3-year EFS in adolescent and young adult. In comparison with the leading role of intensive chemotherapy in pediatric ALL, allogeneic hematopoietic stem cell transplantation (allo-HSCT) plays an important role in treatment strategy of adult ALL. According to the state-of-art understanding of ALL, total therapy of ALL should consist of molecular-cytogenetics classification at diagnosis, minimal residual disease (MRD) monitoring and redefining risk classification during treatment, pediatric-inspired chemotherapy with high-dose Methotrexate/L-asparaginase during consolidation therapy,furthermore,risk/MRD-adapted allo-HSCT for high-risk and refractory/relapsed ALL.In pre-pediatric-inspired protocol era, allo-HSCT still represents the major role for improving the outcome of adult ALL, especially for high-risk and refractory/relapsed ALL. It's established that graft-versus-leukemia (GVL) effect was weak in ALL and patient shows poor response for donor-lymphocyte infusion (DLI). Intensified conditioning regimen allo-HSCT is based on a hypothesis of that intensifying condition with less-used drugs could overcome resistance,reduce tumor burden, and most importantly, spare enough time for slow-growing GVL effect following immune reconstitution to finally get rid of MRD and control the disease. Our previous trial of HDE-ALL-2011 (NCT01457040) have confirmed the role of intensified conditioning allo-HSCT in adult ALL, resulting in significantly improved OS and EFS in comparison with previous standard TBI/CY2 conditioning regimen(data not yet published). But at the same time, FA-TBI/CY2-VP16 conditioning regimen was associated with high transplantation-related mortality (TRM), which might be attributed to excessive suppression on both bone marrow and immune. TT-ALL-HIE-2013, substituting FA with idarubicin, is aimed at maintaining anti-tumor effect with less cross-resistance and immune suppression and reducing TRM.

研究设计

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

入排标准

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

入选标准

  • Age: 16 years to 65 years;
  • Diagnosis of acute lymphoblastic leukemia;
  • Patient receives allo-HSCT;
  • The informed consent form has been signed;

排除标准

  • Patient with severe cardiac dysfunction with less than 50% EF;
  • Patient with severe lung dysfunction;
  • Patient with more than 3 times ULN of serum ALT or AST levels, or with more than 2 times ULN of serum TBIL level, or less than 40% of normal prothrombin time activity (PTA); or with more than 2 times the ULN of serum Cr;
  • Patient with severe active infection;
  • Patient with allergy history about suspected drug in conditioning regimen;
  • Patient with other conditions considered unsuitable for the study.

研究组 & 干预措施

IDA-Etoposide Intensified Conditioning

Experimental

干预措施: IDA (Drug)

IDA-Etoposide Intensified Conditioning

Experimental

干预措施: TBI (Radiation)

IDA-Etoposide Intensified Conditioning

Experimental

干预措施: CTX (Drug)

IDA-Etoposide Intensified Conditioning

Experimental

干预措施: VP-16 (Drug)

Non-IDA Conditioning

Active Comparator

干预措施: TBI (Radiation)

Non-IDA Conditioning

Active Comparator

干预措施: CTX (Drug)

Non-IDA Conditioning

Active Comparator

干预措施: VP-16 (Drug)

结局指标

主要结局

Event-Free Survival

时间窗: 3 year

次要结局

  • Transplantation-Related Mortality(3 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (13)

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