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NCT00186888CompletedPhase 3

Study of Treatment for Patients With Cancer of the Eye -Retinoblastoma

Protocol for the Study and Treatment of Patients With Intraocular Retinoblastoma

Source: ClinicalTrials.gov · Last updated 4 Sept 2025

Brief summary (registry, in English)

Retinoblastoma is a childhood cancer which affects the retina of the eye. The retina is the light sensitive layer of tissue that lines the back of the eyeball; sends visual messages through the optic nerve to the brain. When only one eye is affected, this is known as unilateral retinoblastoma and when both eyes are affected, it is called bilateral retinoblastoma. Treatment for retinoblastoma is individualized for each patient and is based on the form and the stage of the disease (inside the eye or has moved outside). The main goal is always to cure the cancer, and save the life of the child. Treatments are also designed with the hope of saving the vision, while completely destroying the tumor. Therapies may involve surgery, chemotherapy, radiation, and other treatments called focal treatments. Focal treatments may be laser therapy, freezing, or heat treatments meant to shrink and kill the tumor. In this study, researchers want to investigate how different participants respond to different therapies that are individualized specifically for them. Participants will be divided into three main groups, depending on whether the disease is unilateral or bilateral, and the stage of the disease. One of the main objectives of the study is to investigate how advanced tumors in children with bilateral disease respond to a new combination of chemotherapy with topotecan and vincristine, with G-CSF support. In order to improve results, some children with very advanced disease may receive carboplatin chemotherapy given around the eye at the same time that they receive topotecan by vein. Also, because children with retinoblastoma are diagnosed so early in life and the vision may be significantly impaired, this study will investigate how children develop and how the brain adjusts and compensates for the visual deficits. Finally, this study also investigates the biology of retinoblastoma, in order to understand better how this cancer develops.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
107 (actual)
First submitted
12 Sept 2005
Start date
7 Apr 2005
Primary completion date
Nov 2013
Lead sponsor
St. Jude Children's Research Hospital
NCT number
NCT00186888

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 107
  • From 7 Apr 2005 to the primary completion date, Nov 2013
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously treated patients

Other illness

  • Presence of metastatic disease or orbital involvement
  • Patients must not have an invasive infection at time of protocol entry.

Who the study is looking for

  • Must have newly diagnosed intraocular retinoblastoma, previously untreated. Patients previously diagnosed with unilateral retinoblastoma treated surgically (or with focal therapies), who develop asynchronous involvement of the contralateral eye, will be eligible for study.
  • Must have a life expectancy of at least 8 weeks.
  • Must have Performance Status (ECOG) of 0-2.
  • Patients must have an adequate liver function, as defined by bilirubin less than or equal to 3 x normal, and SGOT and SGPT less than or equal to 3x normal.
  • Patients must have adequate renal function as defined by serum creatinine less than or equal to 3x normal for age.
  • Legal guardians must sign an informed consent indicating that they are aware of this study, its possible benefits, and toxic side effects. Legal guardians will be given a copy of the consent form.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
St. Jude Children's Research Hospital
Coordinator of this site? Confirm its status
MemphisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.