Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
24 participants
OBSERVATIONAL
2013-10-18
2017-05-31
Brief Summary
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Liver iron accumulation has been documented in childhood cancer survivors, however, it is not known if iron associated organ toxicity is contributing to the long-term morbidity that has been well documented among these survivors. This study will investigate the prevalence of iron overload and the association of tissue iron burden with markers of organ dysfunction in leukemia survivors. This study will determine the prevalence of iron overload among long-term leukemia survivors that underwent blood transfusion. This study will use blood and magnetic resonance imaging (MRI) testing to determine iron overload of specified organs. Understanding the prevalence of iron overload could impact surveillance practices in leukemia survivors.
PRIMARY OBJECTIVE:
* To determine the prevalence of iron overload in the liver \[liver iron concentration (LIC) \>3mg/g using R2\* MRI measurements\] and in the heart (T2\* \<20 ms) among long-term leukemia survivors transfused with ≥50ml/kg of packed red blood cells.
SECONDARY OBJECTIVES:
* To examine the relationship between hepatic, cardiac, and endocrine dysfunction and transfusionally acquired iron overload as defined by R2\* and T2\* MRI among survivors of pediatric leukemias.
* To investigate the association between serum ferritin, transferrin saturation, non-transferrin-bound iron, and hepcidin measurements with R2\* and T2\* MRI-defined iron overload.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* At time of enrollment survivors should be \> 5 and \< 10 years from diagnosis of primary cancer.
* A packed red blood cell transfusion history of ≥50 ml/kg.
Exclusion Criteria
* History of hematopoietic stem cell transplant (HSCT)
* A known disorder of iron regulation such as hereditary hemochromatosis
* Any contraindication to undergoing an MRI, such as the presence of ferromagnetic material in the body
* If patient is an adult (18 years or over), does require IV sedation or anxiolytic to undergo MRI
* Positive pregnancy test, or known ongoing pregnancy
5 Years
ALL
No
Sponsors
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Baylor College of Medicine
OTHER
St. Jude Children's Research Hospital
OTHER
Responsible Party
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Principal Investigators
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Jane Hankins, MD, MS
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Locations
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St. Jude Children's Research Hospital
Memphis, Tennessee, United States
Countries
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Related Links
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St. Jude Children's Research Hospital
Clinical Trials Open at St. Jude
Other Identifiers
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TRIALS
Identifier Type: -
Identifier Source: org_study_id
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