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Proton Beam Radiation Therapy for Intraocular and Periocular Retinoblastoma

Primary Purpose

Retinoblastoma

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Proton Beam Radiation Therapy
Ophthalmic EUA
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Retinoblastoma focused on measuring Children with retinoblastoma, Retinoblastoma, Pediatrics, Proton Beam Radiation Therapy, Radiation Therapy, Tumor of the Eye, Ophthalmic EUA, Examination under anesthesia, Bilateral retinoblastoma, Unilateral retinoblastoma, Extraocular disease, Intraocular procedure

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Active or recurrent retinoblastoma patient eligible for treatment of external beam radiation therapy.
  2. A parent or guardian who can provide informed consent to a minor or child participant.
  3. No concurrent infection.
  4. No contraindication for repeated general anesthesia/sedation.

Exclusion Criteria:

  1. Inability to return for multiple examinations under anesthesia.
  2. Medical contraindication for exams under anesthesia/sedation.
  3. Unreliable follow-up.

Sites / Locations

  • UT MD Anderson Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Proton Beam Radiation Therapy

Arm Description

Radiation given daily for 5 days in a row each week (except for Saturdays, Sundays, and holidays). The whole treatment will take about 4-6 weeks. Ophthalmic examination under anesthesia including dilated eye exam, ocular fundus photography (Ret-Cam), ocular echography and neuro-radiologic assessment (as deemed necessary)

Outcomes

Primary Outcome Measures

Rate of Local Control in the Globe at 12 Months
Where proton beam radiation therapy used as an alternative to external photon beam irradiation in children with retinoblastoma as a means of local tumor control and ocular retention, local tumor control measured for participants with a globe as tumor regression with ocular retention, and for post enucleation measured as lack of orbital tumor recurrence.

Secondary Outcome Measures

Full Information

First Posted
February 5, 2007
Last Updated
February 12, 2015
Sponsor
M.D. Anderson Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT00432445
Brief Title
Proton Beam Radiation Therapy for Intraocular and Periocular Retinoblastoma
Official Title
A Phase II Trial of Proton Beam Radiation Therapy for Intra- and Periocular Retinoblastoma
Study Type
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Terminated
Why Stopped
Low accrual.
Study Start Date
January 2007 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this trial is to evaluate proton beam radiation therapy as an alternative to external photon beam irradiation in children with retinoblastoma as a means of local tumor control and ocular retention.
Detailed Description
External photon beam radiation therapy (which is current standard of care) has been used in the treatment of retinoblastoma. It is a form of radiation therapy in which the radiation is delivered by a machine pointed at the area to be radiated. Proton beam radiation therapy is a form of external photon beam radiation therapy, but it may be more effective because its adjusted dosing delivers less radiation to surrounding areas of the tumor, which helps preserve other tissues and cause fewer side effects. Before you can start treatment on this study, you will have what are called "screening tests." These tests will help the doctor decide if you are eligible to take part in this study. Your eye doctor will perform an assessment of your eye, including an exam while you are under anesthesia. This exam will include a dilated eye exam, photography of your affected eye (by a Ret-Cam), ultrasound of your affected eye, and imaging scans, such as computed tomography (CT) or magnetic resonance imaging (MRI), if the doctor thinks it is necessary. The assessments will be done to check and confirm the status of the disease. After diagnosis of retinoblastoma, the study doctor will first see if external photon beam radiation therapy is a reasonable treatment option for you. If external photon beam radiotherapy is deemed appropriate for you, you will be eligible to receive proton beam radiation therapy in this study. If you are found to be eligible to take part in this study, you will be treated with proton beam radiation therapy. Treatment will begin within 1 week of referral to the M. D. Anderson Proton Center. It will be given daily for 5 days in a row each week (except for Saturdays, Sundays, and holidays). The whole treatment will take about 4-6 weeks. Within 2-4 weeks after completion of therapy, you will have an eye exam performed under anesthesia (like the one during screening). You will have repeated eye exams under anesthesia, depending on the appearance and response of the tumor to therapy. This will occur about every 1-4 months. You will continue to have these eye exams until the tumors are considered to be stable or unless your disease gets worse. If the disease gets worse or you experience any intolerable side effects, you may be taken off treatment. You will be required to have lifelong eye and medical assessments to continue to monitor you for disease. If no disease is found 5 years after completion of proton beam radiation therapy, you will be considered free of disease. You will then have annual (yearly) eye and pediatric assessment through adulthood. This is an investigational study. Up to 20 patients will take part in this study. All will be enrolled at M.D. Anderson.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinoblastoma
Keywords
Children with retinoblastoma, Retinoblastoma, Pediatrics, Proton Beam Radiation Therapy, Radiation Therapy, Tumor of the Eye, Ophthalmic EUA, Examination under anesthesia, Bilateral retinoblastoma, Unilateral retinoblastoma, Extraocular disease, Intraocular procedure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Proton Beam Radiation Therapy
Arm Type
Experimental
Arm Description
Radiation given daily for 5 days in a row each week (except for Saturdays, Sundays, and holidays). The whole treatment will take about 4-6 weeks. Ophthalmic examination under anesthesia including dilated eye exam, ocular fundus photography (Ret-Cam), ocular echography and neuro-radiologic assessment (as deemed necessary)
Intervention Type
Radiation
Intervention Name(s)
Proton Beam Radiation Therapy
Intervention Description
Radiation given daily for 5 days in a row each week (except for Saturdays, Sundays, and holidays). The whole treatment will take about 4-6 weeks.
Intervention Type
Procedure
Intervention Name(s)
Ophthalmic EUA
Other Intervention Name(s)
eye exam, ophthalmic exam
Intervention Description
Ophthalmic examination under anesthesia including dilated eye exam, ocular fundus photography (Ret-Cam), ocular echography and neuro-radiologic assessment (as deemed necessary)
Primary Outcome Measure Information:
Title
Rate of Local Control in the Globe at 12 Months
Description
Where proton beam radiation therapy used as an alternative to external photon beam irradiation in children with retinoblastoma as a means of local tumor control and ocular retention, local tumor control measured for participants with a globe as tumor regression with ocular retention, and for post enucleation measured as lack of orbital tumor recurrence.
Time Frame
12 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active or recurrent retinoblastoma patient eligible for treatment of external beam radiation therapy. A parent or guardian who can provide informed consent to a minor or child participant. No concurrent infection. No contraindication for repeated general anesthesia/sedation. Exclusion Criteria: Inability to return for multiple examinations under anesthesia. Medical contraindication for exams under anesthesia/sedation. Unreliable follow-up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dan Gombos, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
UT MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.mdanderson.org
Description
MD Anderson Cancer Center website

Learn more about this trial

Proton Beam Radiation Therapy for Intraocular and Periocular Retinoblastoma

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