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Active Not RecruitingNCT00110110

Combination Chemotherapy and Cyclosporine Followed by Focal Therapy for Bilateral Retinoblastoma

Multicenter Phase II Study for International Intraocular Retinoblastoma Classification Groups B, C & D Tumors Treated With Carboplatin-Etoposide-Vincristine-Cyclosporine-Focal Therapy Multimodality Protocol (OCRN Multicenter RB 2003)

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
71 (estimated)
Sponsor
The Hospital for Sick Children · Academic / Other
Sex
All
Age
30 Days
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as carboplatin, etoposide, and vincristine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Sometimes when chemotherapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to chemotherapy. Giving cyclosporine together with chemotherapy may reduce drug resistance and allow the tumor cells to be killed. Cryotherapy kills tumor cells by freezing them. Laser therapy uses light to kill tumor cells. Giving combination chemotherapy together with cyclosporine followed by cryotherapy and/or laser therapy may be an effective treatment for retinoblastoma. PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with cyclosporine followed by cryotherapy and/or laser therapy works in treating patients with newly diagnosed retinoblastoma in both eyes.

Detailed description

OBJECTIVES: Primary * Compare the efficacy of neoadjuvant high-dose carboplatin and etoposide, vincristine, and cyclosporine (CSA) followed by ophthalmic focal therapy comprising cryotherapy and/or laser therapy to historical world data of chemotherapy treatment without CSA, in terms of increasing the proportion of eyes that remain relapse free and do not require external beam radiotherapy and/or enucleation, in patients with newly diagnosed Group B, C, or D bilateral intraocular retinoblastoma. Secondary * Determine the toxicity of this regimen in these patients. OUTLINE: This is a multicenter study. Patients receive high-dose carboplatin IV over 30 minutes on day 1; vincristine IV over 5 minutes and high-dose etoposide IV over 25 minutes on day 2; cyclosporine IV over 1 hour before chemotherapy and then over 2 hours after chemotherapy on days 1 and 2, and filgrastim (G-CSF) subcutaneously once daily beginning on day 3 and continuing until day 16 or until blood counts recover. Treatment repeats every 21 days for a total of 3 courses for patients with Group B disease and a total of 6 courses for patients with Group C or D disease. Patients undergo eye examination under anesthesia (EUA) at initial staging and then before each course of chemotherapy. Patients with small peripheral tumors in eyes without retinal detachment undergo minimal focal therapy (mainly cryotherapy) during EUA at initial staging and then after chemotherapy courses 1 and 2. At EUA after the third and subsequent courses of chemotherapy, patients with tumors that have sufficiently reduced in size undergo additional cryotherapy or laser therapy. After completion of chemotherapy, patients with any suspicious, active, or reactivated tumor undergo additional cryotherapy and/or laser therapy during EUA approximately every 4-8 weeks (or at longer intervals) for up to 5 years (as needed). After completion of study chemotherapy, patients are followed every 3 months for 2 years, every 6 months for 2 years, and then annually for 1 year. PROJECTED ACCRUAL: A total of 71 patients will be accrued for this study within 2.4 years.

Conditions

Interventions

TypeNameDescription
BIOLOGICALfilgrastimGiven after chemo cycle for 7 days or until neutrophil counts return to normal.
DRUGCarboplatinGiven at 28 mg/kg/dose.
DRUGCyclosporineGiven at 33 mg/kg/dose
DRUGEtoposideGiven at 12 mg/kg/dose
DRUGvincristine sulfateGiven at 0.025 mg/kg/dose for the first cycle and 0.05 mg/kg/dose for subsequent cycles if first cycle well-tolerated
PROCEDUREcryosurgeryLocal application of extreme cold to destroy residual tumor.
PROCEDURElaser therapyLocal and precise application of laser beams to destroy residual tumor.

Timeline

Start date
2004-06-01
Primary completion
2016-04-20
Completion
2024-12-31
First posted
2005-05-04
Last updated
2024-04-17

Locations

6 sites across 4 countries: Canada, Chile, India, Singapore

Source: ClinicalTrials.gov record NCT00110110. Inclusion in this directory is not an endorsement.