Actively Recruiting
Interest of Individual Biomarkers From the Identification of Tumor Genotype in Plasma (ctDNA) by High-throughput Molecular Next Generation Techniques in the Diagnosis and Management of Lymphomas
Led by Centre Hospitalier Universitaire Dijon · Updated on 2025-06-11
1200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Lymphomas are the most common blood cancers, with diffuse large B-cell lymphoma (DLBCL), Hodgkin's lymphoma (HL), and follicular lymphoma (FL) being the three most frequent types. Treatments for these lymphomas often aim to cure. Positron emission tomography (PET) is currently used to guide treatment by balancing effectiveness and side effects, adjusting treatment intensity based on patient response. Researchers are exploring additional methods, such as circulating tumor DNA (ctDNA) analysis using advanced sequencing techniques, to better characterize lymphoma before and during treatment and to improve patient management. This study collects plasma samples from patients diagnosed with one of the common lymphomas before treatment, during therapy, and for two years afterward. It focuses on identifying tumor DNA in the blood using high-throughput molecular techniques like CAPP-Seq, PhAsE Seq, and VIRCAPP-seq. The goal is to evaluate whether monitoring ctDNA alongside PET scans can help tailor treatment more precisely, detect relapses earlier, and manage patients with poor responses more effectively. The study also includes less common lymphoma subtypes such as mantle cell lymphoma and T-cell lymphoma. Participants will provide blood samples at various points throughout their treatment and follow-up period, which averages seven years. Researchers will analyze these samples to track biomarkers and tumor mutation profiles over time. The study monitors patients without altering their prescribed treatment plans and aims to gather data that may inform personalized lymphoma management in the future. The trial is non-randomized and observational in nature, focusing on long-term biomarker evaluation and patient outcomes.
CONDITIONS
Brief Title
Interest of Individual Biomarkers From the Identification of Tumor Genotype by High-throughput Molecular Techniques
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Person who has not opposed their inclusion in the trial
- Confirmed diagnosis of one of these lymphomas: diffuse large B-cell lymphoma, follicular lymphoma, classic Hodgkin's lymphoma, T-cell lymphoma, or mantle cell lymphoma according to WHO 2016 classification
- Not currently receiving treatment for lymphoma or have only received corticosteroids within 14 days before first sampling, limited to 500 mg total dose
- Requires systemic treatment within 30 days of screening
You will not qualify if you...
- Person under legal protection such as curatorship or guardianship
- Person under partial judicial control
- Pregnant, parturient, or breastfeeding women
- Adults unable to express non-opposition to participation
- Minors
- Localized lymphoma treated only by surgery or localized radiotherapy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Through study completion, an average of 7 years
Participants provide blood samples to identify tumor genotype biomarkers and mutation profiles using high-throughput molecular techniques over time.
Periodic blood sampling visits over 7 years
Trial Site Locations
Total: 1 location
1
Chu Dijon Bourgogne
Dijon, France, 21000
Actively Recruiting
Research Team
C
Cédric ROSSI
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
5
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