Iron Overload in Pediatric Oncology Patients

Sponsor
Northwell Health (Other)
Overall Status
Completed
CT.gov ID
NCT01034072
Collaborator
Novartis (Industry)
75
1
25
3

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate for iron overload in pediatric oncology and transplant patients who have completed their treatment between one to ten years ago.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Long term survivors of childhood cancer, are a distinct group requiring specific follow-up in order to enhance their quality of life. Studies have shown that many of these patients will go on to develop chronic issues within different organ systems. Because of the iron burden of the frequent transfusions required to care for these patients, iron overload may indeed be one of the problems these survivors potentially face. Research primarily in thalassemia and bone marrow transplant patients who were extensively transfused has shown that iron overload can have a significant impact on their overall health. Complications from increased iron burden can include growth retardation, gonadal dysfunction, hypothyroidism, impaired glucose metabolism, cardiac arrhythmias and failure, hepatic fibrosis and cirrhosis, and increased susceptibility to infections. However all of these conditions related to iron overload can be prevented with the use of either phlebotomy or chelation therapy. Based on this knowledge, our objective is to determine if pediatric oncology and transplant patients heavily supported with transfusions develop consequential biochemical and clinical evidence of iron overload.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    75 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Evaluation of Iron Overload in Pediatric Oncology and Hematopoietic Stem Cell Transplant Patients
    Actual Study Start Date :
    Dec 1, 2009
    Actual Primary Completion Date :
    Jan 1, 2012
    Actual Study Completion Date :
    Jan 1, 2012

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of iron overload in pediatric oncology and transplant patients post-treatment. [1-10 years]

      Prevalence of iron overload in pediatric oncology and transplant patients post-treatment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    78 Months to 25 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients six and a half to twenty five years of age with a history of acute myelogenous leukemia, rhabdomyosarcoma, Ewing sarcoma, osteosarcoma, and neuroblastoma who have completed their treatment or received their last packed red blood cell transfusion at least one year prior to enrollment (which ever occurred later) and are one to ten years post-treatment.

    • Patients six and a half to twenty five years of age who have undergone hematopoietic stem cell transplant for any malignancy and are at least one year from their last transfusion or transplant date prior to enrollment (which ever occurred later) and are one to ten years post-transplant.

    • Patients who were treated at Schneider Children's Hospital or at Children's Hospital of Philadelphia.

    Exclusion Criteria:
    • Patients who have clinical evidence of chronic graft vs. host disease of skin, liver or gastrointestinal tract.

    • Patients with a chronic infection (viral hepatitis), liver disease (fibrosis, cirrhosis), or a history of radiation to the liver.

    • Patients who cannot have an MRI due to metallic implants (i.e. pacemakers, prosthetic valves, etc.)

    • Patients who are pregnant.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Feinstein Institute for Medical Research Manhasset New York United States 11030

    Sponsors and Collaborators

    • Northwell Health
    • Novartis

    Investigators

    • Principal Investigator: Jonathan Fish, MD, Feinstein Institute for Medical Research

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jonathan Fish, Physician, Northwell Health
    ClinicalTrials.gov Identifier:
    NCT01034072
    Other Study ID Numbers:
    • 09-116
    First Posted:
    Dec 17, 2009
    Last Update Posted:
    Apr 11, 2018
    Last Verified:
    Apr 1, 2018
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 11, 2018