CTOP/ITE/MTX Compared With CHOP as the First-line Therapy for Newly Diagnosed Young Patients With T Cell Lymphoma

Sponsor
Ruijin Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01746992
Collaborator
(none)
200
1
2
75
2.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Cyclophosphamide 750mg/m2
  • Drug: Vincristine 1.4mg/m2
  • Drug: Doxorubicin 50mg/m2
  • Drug: prednisone 60mg/m2
  • Drug: ifosfamide 2000mg/m2
  • Drug: pirarubicin 50mg/m2
  • Drug: pirarubicin 25mg/m2
  • Drug: Etoposide phosphate 100mg/m2
  • Drug: methotrexate 1500mg/m2
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
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
Study Start Date :
Sep 1, 2012
Anticipated Primary Completion Date :
Sep 1, 2018
Anticipated Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: pirarubicin

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

Drug: Cyclophosphamide 750mg/m2
day 1 in both arms
Other Names:
  • CTX
  • Drug: Vincristine 1.4mg/m2
    day 1
    Other Names:
  • VCR
  • Drug: prednisone 60mg/m2
    day1-day5
    Other Names:
  • PRED
  • Drug: ifosfamide 2000mg/m2
    day 22-day 24
    Other Names:
  • IFO
  • Drug: pirarubicin 50mg/m2
    day 1
    Other Names:
  • THP
  • Drug: pirarubicin 25mg/m2
    day 22
    Other Names:
  • THP
  • Drug: Etoposide phosphate 100mg/m2
    day 22-day 24
    Other Names:
  • VP-16
  • Drug: methotrexate 1500mg/m2
    day 43
    Other Names:
  • MTX
  • Active Comparator: doxorubicin

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

    Drug: Cyclophosphamide 750mg/m2
    day 1 in both arms
    Other Names:
  • CTX
  • Drug: Vincristine 1.4mg/m2
    day 1
    Other Names:
  • VCR
  • Drug: Doxorubicin 50mg/m2
    day 1
    Other Names:
  • ADM
  • Drug: prednisone 60mg/m2
    day1-day5
    Other Names:
  • PRED
  • Outcome Measures

    Primary Outcome Measures

    1. complete remission rate [6 months]

    2. 3-year PFS [3 years]

    Secondary Outcome Measures

    1. overall response rate [6 months]

    2. 3-year os [3 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 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

    Exclusion Criteria:
    • 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ruijin hospital Shanghai Shanghai China 200025

    Sponsors and Collaborators

    • Ruijin Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Zhao Weili, vice director of Department of Hematology, Ruijin Hospital
    ClinicalTrials.gov Identifier:
    NCT01746992
    Other Study ID Numbers:
    • CTOP
    First Posted:
    Dec 11, 2012
    Last Update Posted:
    Nov 14, 2017
    Last Verified:
    Nov 1, 2017

    Study Results

    No Results Posted as of Nov 14, 2017