Actively Recruiting

All Genders
ID03267459

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of grade B to D retinoblastoma
  • Planned treatment with intra-arterial chemotherapy
Not Eligible

You will not qualify if you...

  • none

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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)

Monitoring

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

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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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