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Phase 3 N=105 Treatment

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

Retinoblastoma · Retinal Neoplasm

Enrolled (actual)
105
Serious AEs
10.5%
Results posted
Aug 2011
Primary outcome: Primary: Stratum B Response to Window Therapy — 24; 2; 1 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Enucleation (Procedure); Vincristine, Carboplatin (Drug); Focal Therapies (Procedure); External Beam Radiation (Radiation); Vincristine and Topotecan (Drug); Vincristine + Carboplatin + Etoposide (Drug); vincristine, cyclophosphamide, and doxorubicin (Drug); Vincristine, Carboplatin and Etoposide (Drug); Periocular carboplatin (Procedure); G-CSF (Other)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
St. Jude Children's Research Hospital
Primary completion
Nov 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Stratum B Response to Window Therapy
24; 2; 1
SECONDARY
Stratum B Response Rate of Early Stage Eyes to Window Therapy
11; 0; 1
SECONDARY
Relationship Between Topotecan Clearance (CL) and CYP3A4/5 Genotype in Stratum B Participants.
18.8 0.452
SECONDARY
Relationship Between Topotecan Clearance (CL) and ABCG2/B1 Genotype in Stratum B Participants.
18.8 0.245
SECONDARY
Event-free Survival of Stratum B Patients Responding to Window Treatment
0.667
SECONDARY
Ocular Survival of Stratum B Patients Responding to Window Treatment
0.667
SECONDARY
Event-free Survival of Eyes in Stratum B Patients Responding to Window Treatment
0.763
SECONDARY
Ocular Survival of Eyes in Stratum B Patients Responding to Window Treatment
0.763
SECONDARY
Event-free Survival of Stratum B Patients Not Responding to Window Treatment
SECONDARY
Ocular Survival of Stratum B Patients Not Responding to Window Treatment
SECONDARY
Event-free Survival of Eyes in Stratum B Patients Not Responding to Window Treatment
SECONDARY
Ocular Survival of Eyes in Stratum B Patients Not Responding to Window Treatment
SECONDARY
Event-free Survival of Stratum A Patients
0.688
SECONDARY
Ocular Survival of Stratum A Patients
0.688
SECONDARY
Event-free Survival of Eyes of Stratum B Patients
1.0
SECONDARY
Ocular Survival of Eyes of Stratum B Patients
1.0
SECONDARY
Event-free Survival of Eyes in Stratum A and Stratum B Patients Based on IC Classification
0.839; 0.667; 1.0; 0.743
SECONDARY
Ocular Survival of Eyes in Stratum A and Stratum B Patients Based on IC Classification
0.839; 0.667; 1.0; 0.743
SECONDARY
Event-free Survival Per Eye in Stratum A and Stratum B Patients Based on AJCC Classification
0.857; 0.500; 1.0; 0.719
SECONDARY
Ocular Survival Per Eye in Stratum A and Stratum B Patients Based on AJCC Classification
0.857; 0.500; 1.0; 0.719
SECONDARY
Change in Cognitive Functioning
91.61; 90.96; 95.91; 88.40; 82.12; 86.00
SECONDARY
Change in Relevant Daily Living Skills
97.48; 104.73; 106.06; 94.22; 96.45; 93.03
SECONDARY
Change in Parent Report of Social-Emotional Factors
40; 19.42; 26.28; 29.67; 40.61; 39.93
SECONDARY
Change in Parenting Stress Index (PSI)
96.76; 93.08; 93.27; 92.77; 94.60; 92.49
SECONDARY
Assessment of School Readiness
8.96
SECONDARY
Number of Participants With Development of Pineal Cysts
12; 15; 5; 1; 11
SECONDARY
Number of Participants With Change in Size of Pineal Gland
12; 8; 23
SECONDARY
Change in Distortion Product Otoacoustic Emissions (DPOAEs)
17.7; 5.5; 4.5; 16.6; 9.4; 8.2
SECONDARY
Mean Primary Visual Cortex Function: Cluster Size
2372; 1080; 2105
SECONDARY
Mean Primary Visual Cortex Function: Maximum T-value
7.9; 6.2; 8.8

Summary

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.

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • Previously treated patients
  • Presence of metastatic disease or orbital involvement
  • Patients must not have an invasive infection at time of protocol entry.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00186888). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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