Actively Recruiting
Prediction of the Response Using Dynamic Contrast-enhanced MRI Before Intra-arterial Chemotherapy in Children With Retinoblastoma
Led by Fondation Ophtalmologique Adolphe de Rothschild · Updated on 2026-01-05
60
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Retinoblastoma is the most common tumor inside the eye in young children, making up 6% of pediatric cancers before age 5. The survival rate after 5 years is very high at 95 to 97%. Treatments that save the eye are increasingly used, including intra-arterial chemotherapy, which is given directly into the artery. While this treatment works for most children, some may have early disease progression. Researchers want to use a special type of MRI called dynamic contrast-enhanced MRI (DCE-MRI) to find factors that predict how children will respond to this chemotherapy. Children in the study will have DCE-MRI scans added to their regular MRI before starting intra-arterial chemotherapy. This imaging technique tracks blood flow and tissue changes in the eye to help predict treatment response. The study focuses on children with grade B to D retinoblastoma who are prescribed this chemotherapy treatment. There are no exclusion criteria listed. Participants will be followed for 18 months to see how they respond to chemotherapy. Researchers will evaluate the MRI results alongside treatment outcomes to identify early signs of response or progression. This observational study does not involve additional treatments but collects imaging and clinical data to improve understanding of retinoblastoma treatment response over time.
CONDITIONS
Brief Title
Can Pretreatment MRI be Used to Predict Intra-arterial Chemotherapy Response in Retinoblastoma?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of grade B to D retinoblastoma
- Planned treatment with intra-arterial chemotherapy
You will not qualify if you...
- none
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 - At start of chemotherapy
Participants undergo a dynamic contrast-enhanced MRI examination performed at the beginning of intra-arterial chemotherapy.
1 visit (in-person)
Duration - Up to 18 months
Participants are observed to assess response to chemotherapy over time.
Visits scheduled as part of routine care
Trial Site Locations
Total: 1 location
1
Fondation A De Rothschild
Paris, France, 75019
Actively Recruiting
Research Team
L
Laurence Salomon, MD PhD
A
Augustin Lecler, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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