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临床试验/NCT01746992
NCT01746992Unknown4 期

An Open-label,Multicenter Randomised Study of CTOP/ITE/MTX Compared With CHOP as the First-line Therapy for the New Diagnosed Young Patients With T Cell Non-hodgkin Lymphoma

Ruijin Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2012年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
200
试验地点
1
主要终点
complete remission rate

研究概览

简要总结

T cell lymphoma is a heterogenic malignancy with poor outcome. Five-year PFS and OS of the patients recieved classic CHOP regimen(cyclophosphamide,vincristin,doxorubicin and predisone)is less than 30%.High dose intensive chemotherapy doesn't demonstrate better response. At present, there is no standardized treatment protocol for this kind of lymphoma.

Between 1994 and 1998,the Scotland and Newcastle Lymphoma Group prospectively collected data on newly diagnosed patients with enteropathy associated T-cell lymphoma (EATL)in the Northern Region of England and Scotland,which is a rare and aggressive type of peripheral T-cell lymphoma.The novel regimen IVE/MTX (ifosfamide, vincristine, etoposide/methotrexate)-ASCT was piloted for patients eligible for intensive treatment,followed by auto-stem cell transplantation.Five-years PFS and OS were 52% and 60% respectively, significantly improved compared with the historical group treated with anthracycline-based chemotherapy. The encouraged results were extended to the peripherial T cell lymphoma-non specified(PTCL-nos).

Past studies suggested pirarubicin was more active to the T cell lymphoma than doxorubicin in vitro based on its high concentration in tumor cells. Clinical data also presented equivalent even superior efficacy of pirarubicin with lower toxicity than doxorubicin. The aim of our study is to compare the response and survival rate of CTOP/ITE/MTX (cyclophosphamide, vincristin,pirarubicin and predisone/ ifosfamide, pirarubicin, etoposide/methotrexate) with those of CHOP regimen,looking forward to its superiority in efficacy and safety for the de novo young patients with T cell lymphoma.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • pathologic verified mature T cell lymphoma,including ALK-negative anaplastic large cell lymphoma,peripherial T cell lymphoma-non specific type,angioimmunoblastic T cell lymphoma,enteropathy associated T cell lymphoma and hepatosplenic T cell lymphoma
  • SGOT/SGPT no more than 2 times of UNL
  • serum creatinine no more than 1.5 times of UNL
  • signed informed consent

排除标准

  • woman in pregnancy or lactation
  • allergic to any intervention drug
  • insuitable to the study due to severe complication
  • enrolled to other study during the past 6 months

研究组 & 干预措施

doxorubicin

Active Comparator

8 cycles of CHOP regimen(cyclophosphamide,vincristin,doxorubicin and prednisone)

干预措施: prednisone 60mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: Cyclophosphamide 750mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: Vincristine 1.4mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: prednisone 60mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: ifosfamide 2000mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: pirarubicin 50mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: pirarubicin 25mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: Etoposide phosphate 100mg/m2 (Drug)

pirarubicin

Experimental

3 cycles of CTOP(cyclophosphamide,vincristin,pirarubicin and prednisone),3 cycles of ITE(ifosfamide, pirarubicin, etoposide)and 2 cycles of methotrexate

干预措施: methotrexate 1500mg/m2 (Drug)

doxorubicin

Active Comparator

8 cycles of CHOP regimen(cyclophosphamide,vincristin,doxorubicin and prednisone)

干预措施: Cyclophosphamide 750mg/m2 (Drug)

doxorubicin

Active Comparator

8 cycles of CHOP regimen(cyclophosphamide,vincristin,doxorubicin and prednisone)

干预措施: Vincristine 1.4mg/m2 (Drug)

doxorubicin

Active Comparator

8 cycles of CHOP regimen(cyclophosphamide,vincristin,doxorubicin and prednisone)

干预措施: Doxorubicin 50mg/m2 (Drug)

结局指标

主要结局

complete remission rate

时间窗: 6 months

3-year PFS

时间窗: 3 years

次要结局

  • overall response rate(6 months)
  • 3-year os(3 years)

研究者

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

Zhao Weili

vice director of Department of Hematology

Ruijin Hospital

研究点 (1)

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