Phase
Condition
Retinoblastoma
Treatment
N/AClinical Study ID
Ages 6-6 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients with unilateral RTB.
Patients with advanced intraocular involvement, corresponding to Stage D of theInternational Classification , selected by the Tumour Committee of the RetinoblastomaUnit. By contrast to most other cancers, histological confirmation is contraindicated in RTBprior to onset of treatment and, in our study, any biopsy of the tumour practiced wasconsidered as an exclusion criterion.
The only alternative to treatment is enucleation.
Over six months old at diagnosis and younger than six years old.
Informed consent of the parents or legal representative.
Exclusion
Exclusion Criteria:
Under 6 months old at diagnosis.
Impaired kidney function, with creatinine clearance lower than 80 mL/min/1.73m2 orserum creatinine higher than 0.7 mg/dL.
Impaired liver function, normal function being defined as presenting total bilirubinlevels lower than 1.5 times the limit of normal for that age and ALT lower than 5times the limit of normal for that age.
Patients with some type of coagulation disorder that could contraindicate theprocedure or with a previous diagnosis of any thrombotic condition.
Congenital cerebral anomalies diagnosed previously or detected by angioresonance priorto treatment for extraocular involvement by RTB shown by image techniques,cerebrospinal fluid (CSF) cytology or cytomorphology of bone marrow aspirates (BMA),or positive expression of GD2 synthase in CSF or BMA.
Patients with heart disease, arterial hypertension, or diseases of the nervous systemnot referred to in point 5, or with active infections that the Anaesthesiology Serviceresponsible for the procedure have studied and consider to contraindicate theprocedure.
Not having been selected for intra-arterial chemotherapy through the ophthalmic arteryfor any other reason than those given by the Tumour Committee of the RTB Unit of theHSJD.
Concurrent administration of any other anti-cancer treatment.
Any surgical or non-surgical procedure that could have changed the structure of theeye and, therefore, facilitate risk of dissemination, including histologicalconfirmation prior to treatment.
Participation in another clinical trial.
Study Design
Study Description
Connect with a study center
Hospital Sant Joan de Déu
Esplugues de Llobregat, Barcelona 08950
SpainSite Not Available

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