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CompletedNCT02504190TEAMUpdated May 20, 2020

Non-interventional Study on TEAM Conditioning in Patients With Lymphoma (TEAM)

An observational study in Lymphoma, sponsored by Association for Training, Education, and Research in Hematology, Immunology, and Transplantation. Completed at 1 site in France. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2020-05-20.

Sponsored by Association for Training, Education, and Research in Hematology, Immunology, and Transplantation · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
95
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Lymphoma is a malignant blood disease sensitive to chemotherapy. In case of relapse after first-line treatment, high-dose chemotherapy conditioning followed by autologous hematopoietic stem cell transplantation (auto-HSCT) improves patient survival and reduces the risk of relapse. Auto-HSCT may also be indicated in the first line in case of aggressive lymphoma at high risk of relapse. BEAM (Carmustine, Etoposide, Aracytine and Melphalan) is the more frequently used high-dose conditioning regimen. Nevertheless, Carmustine is no longer available in Europe.

The investigators have therefore chosen to replace Carmustine by Thiotepa and use the TEAM regimen as the new conditioning. Indeed, Thiotepa is approved by french national agency for the security of drugs (ANSM) for use as part of auto-HSCT conditioning regimen. The results of TEAM regimen in terms of efficacy and toxicity appear similar to those of BEAM. However, no study have been performed prospectively. Only small series and case reports have been reported.

If the study confirms the results of retrospective studies, conditioning by TEAM could become a new standard in auto-HSCT for the treatment of lymphoma.

This study is non-interventional, prospective with 3 centers.

All included patients will receive, according to standard practice and drug label in France, the following diagram:

  1. Conditioning:

    • Thiotepa 8 mg / kg to J-6
    • Etoposide 100 mg / m² / 12 h for 4 days (J-5 to D-2)
    • Aracytine 200 mg / m² / 12 h for 4 days (J-5 to D-2)
    • Melphalan 140 mg / m² on day-1
  2. Transfusion graft: the day D0 with autologous peripheral stem cell transplant
  3. Care supports: Patients will be treated according to the usual procedures of centers participating in the study at the discretion of the investigator.
  4. Follow-up of patients will not be changed by the study.

The main objective of the study is to evaluate the progression-free survival (PFS) of lymphoma patients treated with autologous stem cells after conditioning by TEAM

Secondary objectives are:

  • To evaluate overall survival;
  • To assess the response to treatment;
  • to evaluate the incidence of relapse;
  • to assess the toxic transplant related mortality;
  • to study transplant-related morbidity (infections, nutritional and gastrointestinal toxicity, immune reconstitution).
02

Conditions studied

  • Lymphoma

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Keywords

  • Lymphoma
  • TEAM conditioning
  • autologous stem cells transplantation
03

In context

Lymphoma

5,624 studies on the registry are indexed under Lymphoma; 824 are open to participants now.

This study's enrollment of 95 is below the median of 138 across 633 observational studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

Association for Training, Education, and Research in Hematology, Immunology, and Transplantation is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Lymphoma patients will be recruited in on the French site

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients aged between 18 and 65 years,
  • lymphoma confirmed by biopsy
  • first autologous haematopoietic stem cells transplantation after TEAM conditioning

Exclusion criteria

Exclusion Criteria:

  • VIH, HBV, and/or HCV seropositive
  • Contraindication to autologous stem cell transplantation
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
95 participants (actual)
Patient registry
No

Groups and cohorts

  • lymphoma patients eligible for TEAM conditioning

    Lymphoma Patients who are eligible will be included. Patients will undergo TEAM conditioning regimen followed by autologous haematopoietic stem cells transplantation according to standard practice of the centre and drugs label in France.

06

What researchers measure

Primary outcomes

  1. Progression free survival (PFS)

    Time frame: 1 year after autologous haematopoietic stem cells transplantation

Secondary outcomes

  1. Overall Survival

    Time frame: 100 days and at 1 year after autologous haematopoietic stem cells transplantation

  2. Overall and complete response rate

    Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation

  3. Incidence of relapse

    Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation

  4. Impact of transplant-related mortality

    Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation

  5. Incidence of infections

    Time frame: during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation

  6. Incidence of grade 3-4 side effects

    Time frame: during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation

07

Study locations

1 site
  • Mohamad Mohty
    Paris, 75571, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 20, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02504190
Lead sponsor
Association for Training, Education, and Research in Hematology, Immunology, and Transplantation
Responsible party
Sponsor
First posted
Jul 21, 2015
Start date
Jul 16, 2015
Primary completion
Nov 30, 2019
Completion
Nov 30, 2019
Last update
May 20, 2020

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2020. You cannot join it, but the record below documents what was studied.

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