Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07514715

Proof of Concept for Real-time Multicentric Monitoring of MRD by PET and ctDNA in Aggressive B-Cell Lymphomas

Proof of Concept for Real-time Multicentric Monitoring of Minimal Residual Disease (MRD) by PET and Circulating Tumor DNA (ctDNA) in Aggressive B-Cell Lymphomas

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
129 (estimated)
Sponsor
The Lymphoma Academic Research Organisation · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

RT4 (REAL TIME TAILORED THERAPY) study was designed as a national, multicenter proof of concept aiming to demonstrate the technical and operational capacity of the French Connect network and the Positron Emission Tomography (PET) review network to ensure, within a coordinated framework, real time MINIMAL RESIDUAL DISEASE (MRD) monitoring through ctDNA analysis and centralized review of PET imaging.

Detailed description

Monitoring measurable residual disease (MRD) through the analysis of circulating tumor DNA (ctDNA) in plasma is rapidly emerging as one of the major recent advances in the management of lymphomas. Over the past years, several studies have shown that ctDNA enables a dynamic and highly sensitive assessment of treatment response, surpassing the limitations of conventional approaches based on imaging only. Importantly, these advances do not replace or diminish the role of PET imaging. On the contrary, metabolic imaging and molecular monitoring are increasingly seen as complementary tools. When used together, PET imaging and ctDNA kinetic analysis may dynamically refine risk stratification and enable truly individualized adaptive treatment strategies. However, this synergy between MRD and PET can only influence clinical practice or trial design if results are available throughout patient management within a timeframe compatible with therapeutic decision making.

Conditions

Interventions

TypeNameDescription
OTHERblood testThree blood tests will be performed (one before treatment, one at mid treatment, and one at the end of treatment) for ctDNA analysis.

Timeline

Start date
2026-05-01
Primary completion
2028-10-01
Completion
2028-10-01
First posted
2026-04-07
Last updated
2026-04-13

Locations

30 sites across 1 country: France

Source: ClinicalTrials.gov record NCT07514715. Inclusion in this directory is not an endorsement.