MetVasA (SCT survivors)
Recruiting
Who can enter
Children and adults who had an allogeneic hematopoietic stem cell transplantation (SCT) for myelodysplastic syndrome, leukemia or lymphoma at age less than 18 years (SCT survivors)
In follow-up at the LATER outpatient clinic for late effects after SCT
Goal
Goal
The goal of this study is to discover which SCT survivors have an increased risk of metabolic syndrome, vascular damage and accelerated aging after SCT. Also, we want to investigate whether current lifestyle and previous complications of SCT increases this risk.
Background
Background
A stem cell transplantation (SCT) is an intensive treatment that causes damage to various tissues and may thus lead to problems such as vascular damage and graft-versus-host-disease (transplant disease). This tissue damage can increase the risk of developing chronic health conditions (late effects). Often, this has a negative effect on the quality of life of the survivor.
Previous studies showed that patients who underwent an SCT are at increased risk of developing metabolic syndrome (characterized by overweight, hypertension, elevated blood glucose and cholesterol) and vascular damage, and suggested that these patients may show accelerated aging.
In this study we want to investigate which patients have an increased risk for these late effects. And also whether in the future we may have possibilities to intervene, e.g. with modifications in lifestyle or medication.
With the results, we hope to improve the quality of life of the SCT survivors.
In order to participate in a study please refer to your/your child’s doctor.
Last reviewed
Last reviewed
March 23, 2026
Study details
- Study details
Official title
Metabolic syndrome and vascular damage in relation to accelerated aging in survivors of hematopoietic stem cell transplantation for hematological malignancy (MetVasA)Cancer type
Survivors that had an allogeneic stem cell transplantation for myelodysplastic syndrome, leukemia or lymphomaMaximum number of patients
220Start date
December 12, 2023Status
Open for inclusionLocal principal investigators
Dr. D. Bresters and dr. S.M.H. PluijmSponsor
Princess Máxima Center for pediatric oncologyApproval
The study of this new treatment has been reviewed by an accredited medical research ethics committee. This committee has decided that it is justified to ask patients to participate in this study. More information can be found at: CCMO.
The above information is intended as a brief summary only and may not reflect the most up-to-date information. For full details and the current status of a protocol, physicians can contact the Princess Máxima Center directly.