Scientists create detailed map of Lymphoma's immune environment
NCT ID NCT04696692
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 60 people with diffuse large B-cell lymphoma who were starting standard chemotherapy (R-CHOP). Researchers used advanced single-cell technology to analyze tumor and blood samples over two years. The goal was to find biomarkers that could help predict how well treatment works and track disease changes.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Feb 2021
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patient with histologically confirmed diffuse large B-cell lymphoma with a planned first line treatment by R-CHOP (treatment by R-CHOP should not have been initiated prior to inclusion in the study) 2. Age 18 to 80 years at the time of study entry 3. Archived initial diagnostic tumor specimen available 4. Life expectancy ≥ 3months 5. ECOG Performance status 0-2 6. FDG-avid disease (for PET monitoring) 7. Signed written informed consent 8. Patient able to participate and willing to give informed consent prior performance of any study-related procedures and to comply with the study protocol 9. Patient affiliated to a Social Health Insurance in France Exclusion Criteria: 1. Patient pregnant, or breast-feeding 2. Any condition contraindicated with tumor / blood sampling procedures required by the protocol 3. Central Nervous System (CNS) involvement 4. Known history of positive test for Hepatitis B virus or Hepatitis C virus or Immunodeficiency Virus (HIV) or known acquired immunodeficiency syndrome (AIDS) 5. Any current severe or uncontrolled disease, including, but not limited to ongoing or active infection and auto immune disorders 6. Any psychological, familial, geographic or social situation, according to the judgment of investigator, potentially preventing the provision of informed consent or compliance to study procedure 7. Patient who has forfeited his/her freedom by administrative or legal award or who is under legal protection (curatorship and guardianship, protection of justice) 8. Current participation in any other therapeutic clinical study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Institut Universitaire du Cancer Toulouse - Oncopole
Toulouse, 31059, France
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Other studies related to the condition(s) this trial covers.
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