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Iron Overload in Patients Undergoing Donor Stem Cell Transplant

Iron Overload in Allogeneic Hematopoietic Cell Transplantation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00888316
Enrollment
112
Registered
2009-04-27
Start date
2008-12-31
Completion date
2012-06-30
Last updated
2017-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allogeneic Hematopoietic Cell Transplantation, Cancer, Hematopoietic Stem Cell Transplantation

Keywords

iron overload

Brief summary

RATIONALE: Learning about the effect of excess iron in the liver of patients undergoing donor stem cell transplant may help doctors plan treatment. PURPOSE: This study is investigating the effects of iron overload in patients undergoing donor stem cell transplant.

Detailed description

OBJECTIVES: Primary * Determine the impact of pre-transplant iron overload (defined as liver iron concentration \[LIC\] above normal \[\> 1.8 mg/g\] on an MRI of the liver measuring tissue proton transverse relaxation rates \[R2 MRI\]) on the probability of 1-year overall survival of patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). Secondary * Determine the impact of pre-transplant iron overload on the composite endpoint of non-relapse mortality and complications (e.g., serious infections, hepatic veno-occlusive disease, or organ failure) within 1 year after allogeneic HSCT. * Determine the impact of pre-transplant iron overload on the 1-year cumulative incidence of acute or chronic graft-vs-host disease in patients with acute leukemia or myelodysplastic syndromes undergoing allogeneic HSCT. * Determine the impact of pre-transplant iron overload on the 1-year probability of overall survival and non-relapse mortality in patients undergoing allogeneic HSCT. * Determine the prevalence of pre-transplant iron overload in adult patients undergoing allogeneic HSCT. * Determine the correlation between pre-transplant ferritin levels and LIC on R2 MRI. * Compare the longitudinal measures of serum ferritin levels after allogeneic HSCT in patients with iron overload vs those without iron overload. * Estimate the cumulative incidence of iron overload at 1 year after allogeneic HSCT. OUTLINE: Patients undergo blood sample collection to measure serum ferritin levels at baseline (pre-transplant) and then at 3, 6, 9, and 12 months after transplant. Patients with serum ferritin \> 500 ng/mL also undergo an R2 MRI at baseline (pre-transplant) and at 12 months after transplant to determine liver iron concentration. Patients with serum ferritin \> 500 ng/mL at 12 months after transplant also undergo an R2 MRI.

Interventions

PROCEDUREmagnetic resonance imaging

MRI of the liver will be performed within 30 days prior to HSCT (day 0) and can be done during receipt of conditioning regimen chemotherapy and/or radiation therapy. MRI will also be performed in selected patients at 1 year post-HSCT. This MRI will be done within ± 30 days of their 1-year post-transplant followup date. The R2 MRI is a specific MRI technique and cannot be used for the purpose of general diagnostic imaging. In our study, this modality is being used specifically for the estimation of LIC.

Blood samples will be taken pre-transplant, 3, 6, 9 and 12 months post-transplant

Sponsors

Masonic Cancer Center, University of Minnesota
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Planning to undergo allogeneic hematopoietic stem cell transplantation using either myeloablative or reduced-intensity conditioning * Any diagnosis allowed * Not pregnant * Weight ≤ 350 lbs * Must be able to give written informed consent indicating the investigational nature of the study and its potential risks.

Exclusion criteria

* Claustrophobia * Other contraindication for MRI (e.g., cardiac pacemaker, implanted cardiac defibrillator, aneurysm clips, carotid artery vascular clamp, neurostimulator, insulin or infusion pump, or implanted drug infusion device)

Design outcomes

Primary

MeasureTime frameDescription
Overall Survival1 YearNumber of patients alive at 1 year.

Secondary

MeasureTime frameDescription
Acute and chronic graft-vs-host disease1 Year Post TransplantNumber of patients who had acute and chronic graft versus host disease through 1 year after transplant.
Overall survival and non-relapse mortality1 Year Post TransplantNumber of patients who were alive and did not have any non-relapse mortality events at 1 year post transplant. Determine the impact of pre-transplant iron-overload on 1-year probability of overall survival and of non-relapse mortality in allogeneic HSCT recipients with acute leukemia and myelodysplastic syndrome.
Number of Patients with Iron OverloadBaselinePrevalence of iron overload in patients being considered for allogeneic HSCT
Incidence of non-relapse mortalityUp to 1 YearNumber of patients who died due to serious infections, hepatic venous occlusive disorder (VOD) or organ failure within one year of transplant.
Longitudinal averages of serum ferritin levelsPost TransplantCompare the longitudinal measures of serum ferritin between the no iron-overload and iron-overload groups.
Incidence of iron overload1 Year Post TransplantCompare the longitudinal measures of serum ferritin between the no iron-overload and iron-overload groups.
Ferritin levels and Liver Iron ConcentrationBaseline, and 3, 6, 9, and 12 Months Post TransplantCorrelation between pre-transplant and post-transplant ferritin levels and liver iron concentration on an MRI of the liver measuring tissue proton transverse relaxation rates (R2 MRI)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026