Treatment Protocol for Non-Metastatic Unilateral Retinoblastoma (RbGALOP2)
Unilateral Retinoblastoma
About this trial
This is an interventional treatment trial for Unilateral Retinoblastoma
Eligibility Criteria
Inclusion Criteria:
- Histological diagnosis of retinoblastoma confirmed at participating institutions
- Ophthalmological diagnosis of unilateral retinoblastoma in patients undergoing conservative therapy.
- No prior therapy for retinoblastoma
- Lansky Performance Scale greater or equal to 50
- Normal organ function in those patients assigned for chemotherapy
- Signed informed consent
Exclusion Criteria:
- Patients with unilateral retinoblastoma and germline mutations of the Rb1 gene or family history for retinoblastoma
Sites / Locations
- Hospital JP GarrahanRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Experimental
Low Risk Patients
Higher Risk Patients
Stage II Patients
Patients with buphthalmus
Patients with IRSS stage I, pT1, pT2 and pT3 stage will not receive adjuvant therapy
Patients with IRSS stage I, pT3b, pT3c, pT3d will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan
Patients with Stage II (pT4) will receive 6 cycles of adjuvant chemotherapy plus 6 doses of intrathecal topotecan and orbital radiotherapy
Patients with buphthalmus (cT3c, cT3e) will receive 2 cycles of neo-adjuvant chemotherapy plus 6 doses of intrathecal topotecan followed by secondary enucleation and 6 cycles of adjuvant chemotherapy.