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Clinical Trials/NCT00662090
NCT00662090
Active, Not Recruiting
N/A

Prospective Non-randomized Multi-center Study for Epidemiology and Characterization of Myelodysplastic Syndromes (MDS) and Juvenile Myelomonocytic Leucemia (JMML) in Childhood

University Hospital Freiburg1 site in 1 country260 target enrollmentJanuary 2006

Overview

Phase
N/A
Intervention
Not specified
Conditions
Myelodysplastic Syndromes
Sponsor
University Hospital Freiburg
Enrollment
260
Locations
1
Primary Endpoint
To evaluate the frequency of the different subtypes of MDS in childhood and adolescence by a standardized diagnostic approach
Status
Active, Not Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The aim of the study is to improve the accuracy of diagnosis for children and adolescents with MDS by a standardized review of morphology and standardized cytogenetic and molecular analysis.

The primary objectives of the study are:

  • To evaluate the frequency of the different subtypes of MDS in childhood and adolescence by a standardized diagnostic approach
  • To evaluate the frequency of cytogenetic and molecular abnormalities:

Specifically using array-CGH to evaluate the frequency of subtle chromosomal imbalances, i.e. gains and losses of defined chromosomal regions, and amplifications.

Specifically using mFISH to identify unknown chromosomal aberrations, particularly subtle translocations involving new candidate genes, and to better define chromosomal breakpoints.

The secondary objectives of the study are:

  • To assess survival for children and adolescents with MDS and JMML
  • To evaluate relapse rate, morbidity and mortality in children with MDS and JMML treated by HSCT
Registry
clinicaltrials.gov
Start Date
January 2006
End Date
December 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital Freiburg
Responsible Party
Principal Investigator
Principal Investigator

Charlotte Niemeyer, MD

Prof. Dr. Charlotte Niemeyer, MD

University Hospital Freiburg

Eligibility Criteria

Inclusion Criteria

  • Written informed consent by the caretakers and whenever possible the patient's assent.
  • Confirmed diagnosis of MDS or JMML (morphology, cytogenetics)
  • Myeloid leukemia of Down syndrome (patients aged \> 6 years).
  • Age less than 18 years

Exclusion Criteria

  • Denied informed consent and/or assent by caretakers/patient.
  • Myeloid leukemia of Down syndrome (patients \< 6 years).
  • Participation in another study within the last 4 weeks (except for therapy optimizing studies in cancer or bone marrow failure disorders and studies in diagnostics).

Outcomes

Primary Outcomes

To evaluate the frequency of the different subtypes of MDS in childhood and adolescence by a standardized diagnostic approach

Time Frame: 5 years

To evaluate the frequency of cytogenetic and molecular abnormalities

Time Frame: 5 years

Secondary Outcomes

  • To assess survival for children and adolescents with MDS and JMML(5 years)
  • To evaluate relapse rate, morbidity and mortality in children with MDS and JMML treated by HSCT(5 years)

Study Sites (1)

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