Clinical trial · Interventional
18F-FDG PET Scan and MRI Diffusion.Evaluation of the Early Therapeutic Response of Diffuse Large B-cell Lymphoma
18F-FDG PET Scan and MRI Diffusion : Correlation Study of the Evaluation of the Early Therapeutic Response of Diffuse Large B-cell Lymphoma
NCT03121456CI-TRIAL-00071299LYMPHODTECTunknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Open-label, multicenter, uncontrolled and non-randomized study comparing 18F-FDG PET-Scan and diffusion MRI in the assessment of the early therapeutic response of Diffuse Large B-Cell Lymphoma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Diffuse Large B Cell Lymphoma | Diffuse Large B-Cell Lymphoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 18F-FDG PET SCAN | Other | — | UNRESOLVED |
| MRI DIFFUSION | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 18F-FDG PET SCAN
- description
- REALIZATION OF INITIAL 18F-FDG PET SCAN (PRE THERAPEUTIC), THEN BETWEEN CYCLE 2 DAY 10 AND CYCLE 3 DAY 1 MRI DIFFUSION REALIZATION OF INITIAL MRI DIFFUSION WITHIN 7 DAYS AFTER INITIAL 18F-FDG PET SCAN, THEN WITHIN 7 DAYS AFTER 18F-FDG PET SCAN 1.
- interventionNames
- Other: 18F-FDG PET SCAN
- Other: MRI DIFFUSION
Primary outcomes (1)
- measure
- measurement of the correlation between the Delta SUVmax in PET-TDM (or between the Deauville criteria if the Delta SUVmax is not applicable) and the Delta ADCmax in diffusion MRI.
- timeFrame
- up to 2 years
- description
- scattering MRI in the assessment of the early therapeutic response of diffuse large cell Lymphoma.
Secondary outcomes (3)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 19 Years
Show eligibility criteria text
Inclusion Criteria: * Patient with Diffuse Large B-Cell Lymphoma confirmed histologically * Patient with a tumor mass defined as measurable according to the RECIST 1.1 criteria, * Patient requiring a standard first-line chemotherapy treatment (Rituximab -Cyclophosphamide - Hydroxyadriamycin - Oncovin - Prednisone = R-CHOP every 21 days), * Patient older than 18 years, * Performance status less than or equal to 2, * Biological assessment meeting the following criteria: creatinine \<150 μmol / l or creatinine clearance\> 40 ml / min, total bilirubin \<30 μmol / l, transaminases \<2.5 x ULN * Patient of childbearing age must agree to use Means of effective contraception during the treatment period, * Patient having read the information note and having signed informed consent, * Patient with Health care insurance available. Exclusion Criteria: * History of malignant hemopathy or solid tumor * History of previous chemotherapy * Contraindication to one of the examinations studied (Claustrophobia, Pacemaker ...) * Patient included in another clinical trial for which a period of exclusion is mentioned. * Patient considered to be a vulnerable person; Vulnerable persons are defined in article L1121-5 to - 8: Pregnant women, women who are pregnant, women who are breastfeeding, Persons deprived of their liberty by a judicial or administrative decision, persons who are hospitalized without consent under Articles L. 3212-1 and L. 3213-1 which do not fall under the provisions of Article L. 1121-8 and persons admitted to a health or social institution for purposes other than research Persons who are the subject of a legal protection measure or are unable to give their consent.
References
Publications (0)
Data not yet available
No reference posted for this study.