Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05444712

Transplantation After Complete Response In Patients With T-cell Lymphoma

Peripheral T-cell lymphoma (PTCL) encompasses a broad range of post-thymic (i.e., mature) sub-entities as defined by the 2017 WHO classification. The most common entities are angioimmunoblastic T-cell lymphoma (AITL) and other Tfh-phenotype PTCL or PTCL not otherwise specified (NOS), each representing approximately 20 to 25% of mature T- and NK/T-cell lymphomas. Compared to their B-cell counterparts, most PTCL confer dismal prognosis. In fact, except for anaplastic lymphoma kinase (ALK)-positive systemic anaplastic large cell lymphoma (sALCL), 10-year overall survival for patients with PTCL barely exceeds 30%. Given the infrequency and the heterogeneity of these malignancies, no real consensus on first-line treatment has been established for most PTCL.

The place of autologous stem cell transplantation (ASCT) as a consolidation procedure for patients with PTCL achieving a complete metabolic response after induction is still highly debated. ESMO recommendations and recent guidelines from a committee of the American Society for Blood and Marrow Transplantation currently propose ASCT as first-line therapy for transplant-eligible patients for all patients reaching at least a partial response (PR) after induction. NCCN guidelines (version 2.2017) recommend ASCT or observation in case of metabolic CR but salvage regimen in case of residual disease after induction.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Peripheral T Cell Lymphoma Hemic and Lymphatic Diseases Immune System Diseases Immunoproliferative Disorders Lymphatic Diseases Lymphoma Lymphoma, Non-Hodgkin Lymphoma, T-Cell Lymphoma, T-Cell, Peripheral Lymphoproliferative Disorders Neoplasms Neoplasms by Histologic Type

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chu D'Amiens - Hopital Sud, Amiens, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient ≥ 18 years and < 70 years of age at the time of signing the informed consent form (ICF)
  • Patient fit enough to receive autologous stem cell transplant as a consolidation strategy as assessed by the local investigator
  • Hemoglobin level > 8g/dL (transfusion allowed); Neutrophil count >0.5 G/L; Platelets count > 50 G/L (transfusion allowed) Patient with histologically proven "nodal-type peripheral T-cell lymphoma (PTCL)" (latest WHO classification), not previously treated; as defined by the WHO classification, the following subtypes may be included,
  • PTCL, not otherwise specified
  • Follicular helper T-cell lymphomas: Angioimmunoblastic T-cell lymphoma and nodal PTCL with TFH phenotype and follicular T-cell lymphoma
  • Anaplastic large cell lymphoma, ALK-negative
  • Ann Arbor staging (I-IV) except stage I with normal LDH and PS<2 (i.e. stage I aaIPI 0)
  • Participant with a measurable disease by the Lugano criteria (i.e., longest diameter of a nodal site > 1.5 cm and/or longest diameter of an extranodal site > 1.0 cm and/or a hypermetabolic lesion)
  • FFPE Diagnostic tissue block should be available for central pathology review and ancillary molecular analyses
  • Participant with Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2
  • Estimated minimum life expectancy of 3 months
  • Patient who understood and voluntarily signed and dated an informed consent prior to any study-specific assessments/procedures being conducted
  • Able to adhere to the study visit schedule and other protocol requirements
  • Patient covered by any social security system (France)
  • Patient who understands and speaks one of the country official languages
  • Males with partners of childbearing potential must agree to use effective birth control methods during the study as informed by the investigator in accordance with SmPC of each drugs administrated
  • Females of childbearing potential must agree to use effective birth control methods for at least 28 days before starting treatment; while participating in the study; during treatment interruptions and necessary period after the study as informed by the investigator in accordance with SmPC of each drugs administrated

Exclusion criteria

  • Known central nervous system or meningeal involvement by lymphoma
  • Impaired renal function (calculated MDRD or Cockcroft-Gault Creatinine Clearance < 30 ml/min) or impaired liver function tests (serum total bilirubin level > 2.0 mg/dl [34 µmol/L] (except in case of Gilbert's Syndrome, or documented liver or pancreatic involvement by lymphoma), serum transaminases (AST or ALT) > 3 upper normal limit unless they are related to the lymphoma.
  • The following types of T-cell lymphomas:
  • Adult T-cell lymphoma/leukemia (HTLV-1 related T-cell lymphoma)
  • Extranodal T-cell/NK-cell lymphoma, nasal type
  • Anaplastic large cell lymphoma, ALK-positive type
  • Cutaneous T cell lymphoma (mycosis fungoides, Sézary syndrome)
  • Primary cutaneous CD30+ T-cell lymphoproliferative disorder
  • Primary cutaneous anaplastic T-cell lymphoma
  • Enteropathy-associated T-cell lymphoma
  • Hepatosplenic T-cell lymphoma
  • Subcutaneous panniculitis-like T-cell lymphoma
  • Primary cutaneous gamma-delta T-cell lymphoma
  • Primary cutaneous CD8+ aggressive epidermotropic lymphoma
  • Primary cutaneous CD4+ small/medium T-cell lymphoma
  • Active malignancy other than the one treated in this research. Prior history of malignancies unless the patient has been free of the disease for ≥ 2 years. However, patients with the following history are allowed:
  • Basal or squamous cell carcinoma of the skin
  • Carcinoma in situ of the cervix
  • Carcinoma in situ of the breast
  • Incidental histologic finding of prostate cancer (T1a or T1b) using the tumor, nodes, metastasis clinical staging system
  • Vaccinated with live, attenuated vaccines within 6 months of enrollment
  • Use of any standard or experimental anti-cancer drug therapy before the start of treatment except COP (cyclophosphamide, vincristine, prednisone) in case of (or high risk of tumor lysis syndrome) or etoposide for a maximum of 3 doses (at a maximum dose of 150mg/m2) for HLH (Hemophagocytic Lymphohistiocytosis).
  • A corticosteroids therapy > 1mg/kg lasting more than 14 days prior to Cycle 1 Day 1
  • Positive serology for Human Immunodeficiency Virus (HIV) and Human T-Lymphotrophic Virus (HTLV1)
  • Active Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV) infections defined as:
  • HBV :
  • HBs Ag positive
  • HBs Ag negative, anti-HBs antibody positive and anti-HBc antibody positive with detectable viral DNA
  • HCV :

Anti-VHC antibody positive with detectable viral RNA 9. Pregnant, planning to become pregnant or lactating WOCBP 10. Any significant medical conditions, laboratory abnormality or psychiatric illness likely to interfere with the participation in this clinical study (according to the investigator's decision) 11. Person deprived of his/her liberty by a judicial or administrative decision 12. Person hospitalized without consent 13. Adult person under legal protection

Treatment and study plan

Chemotherapy + follow up

Procedure
  • Chemotherapy administrated every 3 weeks for 6 cycles according to local investigator's choice based on usual practices.
  • An intermediate evaluation will be performed after four cycles by PET-CT (or CT-Scan for non-avid PTCL)
  • A post-induction evaluation by PET-CT or CT-Scan will be done between 3 and 5 weeks after the last chemotherapy drug administration for all patients
  • A last evaluation by PET-CT or CT-Scan will be done between 08 and 12 weeks after the post-induction for all patients

Chemotherapy + ASCT + follow up

Procedure
  • Chemotherapy administrated every 3 weeks for 6 cycles according to local investigator's choice based on usual practices.
  • An intermediate evaluation will be performed after four cycles by PET-CT (or CT-Scan for non-avid PTCL)
  • The fifth or sixth cycles should be used as stem-cell mobilizing chemotherapy for patients with ASCT strategy
  • A post-induction evaluation by PET-CT or CT-Scan will be done between 3 and 5 weeks after the last chemotherapy drug administration for all patients
  • Patients with in Complete Response after 6 cycles will receive a High Dose Therapy as conditioning regimen before transplantation
  • A last evaluation by PET-CT or CT-Scan will be done between 08 and 12 weeks after the post-induction for all patients

Primary outcomes

  1. to assess if ASCT is associated with a significant prolongation of progression-free survival (PFS) for patient with peripheral T-cell lymphoma (PTCL) reaching a complete response (CR) according to the response critter

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    progression-free survival defined time from the date of randomization to the date of first documentation of relapse or progressive disease, death due to any cause, or receipt of subsequent systemic chemotherapy to treat residual or progressive peripheral T-cell lymphoma as determined by the investigator, whichever came first.

Secondary outcomes

  1. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of Overall survival (OS)

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    Overall survival will be measured from the date of randomization to the date of death from any cause

  2. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of Overall response rate (ORR) and Complete Response Rate (CRR)

    Time frame: At the end of ASCT (8-12 weeks after post-induction evaluation)

    Overall Response Rate is defined as the proportion of subjects achieving best overall response of partial metabolic response (PMR) or complete metabolic response (CMR) at the end of ASCT (8-12 weeks after PIE). Assessment of response will be determined by investigator and based on Lugano Response Criteria 2014 (PET-CT-Based Response for FDG-avid lymphomas or CT-Based Response if not).

  3. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of duration of Response (DoR)

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    Duration of response will be measured from the time of attainment of CMR or PMR to the date of first documented disease progression, relapse (based on investigator disease assessment), death from any cause or receipt of subsequent systemic chemotherapy to treat residual or progressive peripheral T-cell lymphoma as determined by the investigator, whichever came first.

  4. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of time to next Treatment (TTNT)

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    TTNT will be measured from the date of randomization to the date of first documented administration of new anti-lymphoma treatment.

  5. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of quality of Life

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    The EuroQol 5 Dimensions questionnaire (EQ5D-5L) will be administered at baseline and every three months during follow-up visit.

  6. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of cost-Effectiveness Analysis

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    Will be expressed as the extra cost per a quality adjusted life year. To assess the mean cost per patient of each group, the number of resources consumed and the amounts refunded will be extracted from the French National Health Insurance Information System. The number of QALYs in each group of the trial will be assessed with survival time and the validated EuroQol 5 Dimensions questionnaire (EQ5D-5L).

  7. Comparison of chemotherapy regimens + ASCT consolidation with chemotherapy regimens alone in terms of budget Impact Analysis

    Time frame: When the last randomized patient has reached two years of follow-up or when 154 events (progression/relapse/new anti-lymphoma treatment/death) occured whichever comes first

    budget impact analysis to assess the potential annual economic impact of the new management recommendation (with or without ASCL) for the French Public Health Insurance System across a 3-year time period.

  8. Adjusted comparison of chemotherapy regimens (CHOP vs CHOEP) in non-sALCL in terms of Overall Response Rate (ORR)

    Time frame: at the end of induction (between 3 and 5 weeks after the last drug administration)

    Overall Response Rate is defined as the proportion of subjects achieving best overall response of partial metabolic response (PMR) at the end of induction. Assessment of response will be determined by investigator and based on Lugano Response Criteria 2014 (PET-CT-Based Response for FDG-avid lymphomas or CT-Based Response if not).

  9. Adjusted comparison of chemotherapy regimens (CHOP vs CHOEP) in non-sALCL in terms of Complete Response rate (CRR)

    Time frame: at the end of induction (between 3 and 5 weeks after the last drug administration)

    complete metabolic response is defined as the proportion of subjects achieving complete metabolic response (CMR) at the end of induction. Assessment of response will be determined by investigator and based on Lugano Response Criteria 2014 (PET-CT-Based Response for FDG-avid lymphomas or CT-Based Response if not).

  10. To evaluate the predictive value of total metabolic tumor volume (TMTV) on PET-CT

    Time frame: at patient enrollment

    Predictive value of TMTV on PET-CT

  11. To Evaluate PET-CT Omics

    Time frame: at patient enrollment

    PET-Omics

  12. The assessment of the early PET-CT predictive value after four cycles of chemotherapy on treatment response according to the IWC (International Workshop Criteria) Lugano 2014

    Time frame: After four cycles of chemotherapy (each cycle is 3weeks)

    Predictive value of an early PET_CT after 4 cycles of chemotherapy on treatment response according to the IWC Lugano 2014

Study contacts

Contact information is provided by the study sponsor or research team.

Emmanuel BACHY, Pr

CONTACT

[email protected]

+33(0) 4 78 86 22 05

Rémy GRESSIN, Dr

CONTACT

[email protected]

+33 (0)4 76 76 57 12

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Acronym: TRANSCRIPT

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Jul 6, 2022
Registry last updated
Sep 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.