Skip to content

"RETINO 2011" : Conservative treatment of patients with retinoblastoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-517275-21-00
Acronym
IC 2011-05
Enrollment
133
Registered
2024-09-05
Start date
2012-02-20
Completion date
Unknown
Last updated
2024-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinoblastoma

Brief summary

For the 3 studies: ocular preservation (absence of secondary enucleation) and absence of external beam radiotherapy at 18 months.

Detailed description

Evaluation or the risk of relapse by fundus examination under general anaesthesia until the age of 4 then without general anaesthesia., Prospective evaluation of the ocular and general side effects (short, medium and long term) of the intravenous chemotherapy, intra-arterial chemotherapy, combined to the local treatment as well as the intra-vitreal injections of melphalan., Evaluation of the response to intra-vitreal chemotherapy by melphalan., Study of the radiation doses received during intra-arterial procedures., Evaluate the number of patients presenting with another tumour.

Interventions

DRUGVINCRISTINE TEVA 1 mg/ml
DRUGsolution injectable
DRUGALKERAN 50 mg poudre et solvant pour solution pour perfusion Melphalan
DRUGsolution à diluer pour perfusion
DRUGsolution pour perfusion
DRUGMELPHALAN

Sponsors

Institut Curie
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 17 Years

Design outcomes

Primary

MeasureTime frame
For the 3 studies: ocular preservation (absence of secondary enucleation) and absence of external beam radiotherapy at 18 months.

Secondary

MeasureTime frame
Evaluation or the risk of relapse by fundus examination under general anaesthesia until the age of 4 then without general anaesthesia., Prospective evaluation of the ocular and general side effects (short, medium and long term) of the intravenous chemotherapy, intra-arterial chemotherapy, combined to the local treatment as well as the intra-vitreal injections of melphalan., Evaluation of the response to intra-vitreal chemotherapy by melphalan., Study of the radiation doses received during intra-arterial procedures., Evaluate the number of patients presenting with another tumour.

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026