Research on the Environment and Children's Health: Retinoblastoma

Sponsor
Memorial Sloan Kettering Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT00582049
Collaborator
University of Pennsylvania (Other), New York Presbyterian Hospital (Other), Milton S. Hershey Medical Center (Other)
78
1
58
1.3

Study Details

Study Description

Brief Summary

The purpose of the research study is to learn more about the causes of retinoblastoma and to identify possible risk factors in the parents of patients with retinoblastoma. This kind of study is called an epidemiology study and is often done by interviewing people with and without the disease. In the case of a childhood disease, the researchers ask about experiences of the parents and children before the disease developed.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of the study is to investigate the role of paternal exposures in the etiology of sporadic heritable retinoblastoma (RBL). The study has a matched case-control design with a sample size of 255 pairs. Cases will be children with sporadic heritable (RBL) identified from eight hospitals that together treat most of the RBL patients in the U.S. and Canada. We will use regional controls matched on year of birth and state/province of residence identified by randomdigit-dialing (RDD). Fathers and mothers of cases and controls will be interviewed by telephone about their occupational, medical, dietary, and personal exposures before the index child's conception. Blood samples will be obtained on cases and their parents for DNA isolation. The case's DNA will be used to characterize the disease-causing RB1 mutation. The parent's DNA will be used to detect the few instances in which a parent also has the RB1 mutation, i.e., the child's RBL is familial rather than sporadic.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    78 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Research on the Environment and Children's Health: Retinoblastoma
    Study Start Date :
    Aug 1, 2003
    Actual Primary Completion Date :
    Jun 1, 2008
    Actual Study Completion Date :
    Jun 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    1

    Cases: retinoblastoma patients

    2

    Controls: first cousins or other blood relatives of the retinoblastoma patients (relative controls) or friends of the retinoblastoma patients or children of friends of the parents (friend controls).

    Outcome Measures

    Primary Outcome Measures

    1. demographic and exposure information by telephone interview [5 years 4 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Cases will be children with sporadic heritable RBL, i.e., bilateral RBL without a family history of the disorder.

    • Cases will be diagnosed with retinoblastoma in an approximately 7-year period, beginning January 1, 1998 and continuing until the sample size is reached.

    • The case family must reside in the continental U.S., Alaska, or Canada.

    • The case family must have a telephone in the household.

    • The patient's physician must give permission to contact the parents of the case.

    • The biologic father or mother of the case must be available and consent to be interviewed.

    • The father or mother must speak English or Spanish.

    • Genetic counseling regarding RB1 gene mutation analysis must be done prior to registration onto study.

    Exclusion Criteria:
    • Cases that do not meet the above criteria will be ineligible to participate and excluded from the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Memorial Sloan-Kettering Cancer Center New York New York United States 10065

    Sponsors and Collaborators

    • Memorial Sloan Kettering Cancer Center
    • University of Pennsylvania
    • New York Presbyterian Hospital
    • Milton S. Hershey Medical Center

    Investigators

    • Principal Investigator: Ira Dunkel, MD, Memorial Sloan Kettering Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00582049
    Other Study ID Numbers:
    • 03-030
    First Posted:
    Dec 28, 2007
    Last Update Posted:
    Jul 4, 2008
    Last Verified:
    Jun 1, 2008
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 4, 2008