Neoadjuvant Carboplatin and Vincristine and Standard Local Ophthalmic Therapy in Treating Patients With Intraocular Retinoblastoma

• Status: Completed
• Trial end date: 2010-01-01
• Target enrollment: 0
• Participant gender: All

Summary

This phase III trial is studying how well giving carboplatin and vincristine together with standard local ophthalmic therapy works in treating children with intraocular retinoblastoma. Drugs used in chemotherapy, such as carboplatin and vincristine, work in different ways to stop tumor from dividing so they stop growing or die. It is not yet known whether neoadjuvant chemotherapy combined with standard local ophthalmic therapy is effective in treating intraocular retinoblastoma.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Children's Oncology Group
• Collaborator: National Cancer Institute (NCI)
• Treatments: Carboplatin; Iodine; Vincristine

Criteria

Inclusion Criteria:

• Newly diagnosed Group B intraocular retinoblastoma meeting 1 of the following criteria:

• Group B tumor(s) in 1 eye

• Group B tumor(s) in both eyes

• Group A tumor in 1 eye and Group B tumor(s) in the other eye

• Group E tumor in 1 eye that has been enucleated and Group B tumor(s) in the remaining eye at the time of enucleation of the Group E tumor

• Defined by the International Classification System for Intraocular Retinoblastoma as follows:

• Group A: Small tumors (≤ 3 mm in greatest dimension) confined to the retina, away from foveola and disc meeting the following criteria:

• More than 3 mm from fovea

• More than 1.5 mm from optic disk

• Group B: Tumors more than 3 mm meeting the following criteria:

• Confined to the retina in any location not in Group A

• Tumor associated subretinal fluid < 3 mm from the tumor margin with no subretinal seeding

• Group E: Must have ≥ 1 of the following present:

• Tumor touching the lens

• Tumor anterior to anterior vitreous face involving ciliary body or anterior segment

• Diffuse infiltrating retinoblastoma

• Neovascular glaucoma

• Opaque media from hemorrhage

• Tumor necrosis with aseptic orbital cellulites

• Phthisis bulbi

• Confirmation of diagnosis by CT scan or MRI of the brain and orbits AND an ophthalmologic evaluation under anesthesia within the past 3 weeks

• No choroidal and/or optic nerve invasion past the lamina cribosa

• No evidence of extraocular retinoblastoma clinically or by head and orbital MRI and/or CT scan

• No tumor present on histological exam at the cut end of the optic nerve for any Group E eye enucleated before study entry

• Performance status - ECOG 0-2

• Bilirubin ≤ 1.5 times upper limit of normal (ULN) for age

• AST or ALT < 2.5 times ULN for age

• Creatinine clearance (based on Schwartz formula) or radioisotope glomerular filtration rate ≥ 70mL/min/1.73 m^2

• No prior chemotherapy

• No other concurrent chemotherapy

• No prior radiotherapy

• No other concurrent radiotherapy, including intensity-modulated stereotactic, or proton beam radiotherapy

• Prior enucleation of one eye allowed provided the remaining eye is Group B

• No concurrent enucleation

• No prior local ophthalmic therapy for retinoblastoma

• No other prior therapy for retinoblastoma

• No local therapy during chemotherapy course 1