Genomic Profiling for Pediatric Leukemia and Related Blood Cancers
This study is looking at the genes of children and young adults (up to age 30) who have leukemia, myelodysplastic syndromes (MDS), or myeloproliferative syndromes (MPS). Genes are like instructions that tell cells how to grow and work. By using "genomic profiling" (a test that looks at these instructions), researchers hope to understand why these diseases develop and why some people respond to treatments differently. This study aims to enroll 300 participants. The main goal is to see how many children with leukemia are enrolled for genomic profiling over three years. The study status is currently unclear, so it's not known if they are actively recruiting.
- Study design
- This is an observational study, meaning researchers will collect information without giving new treatments. It plans to enroll 300 participants.
- What's involved
- A sample of your leukemia will be submitted for genomic profiling. The study will also collect follow-up data on your health and how the genomic profiling affected your treatment.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will collect follow-up data on patient outcome and whether genomic profiling influenced treatment, but a specific duration is not mentioned.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Genomically Profiling, Collecting, Archiving and Distributing Hematologic Malignancy Specimens
At a glance
Conditions
Where it's being run
8 sites across 7 statesStudy leadership
- Yana Pikman, MD · PRINCIPAL_INVESTIGATOR · Dana-Farber Cancer Institute
Who to contact
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Do you actually qualify for this trial?
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Inclusion
What this trial measures
- Number of Patients Enrolled for Genomic Profiling-Pediatric Leukemia3 Years
To perform genomic profiling of pediatric leukemia using clinical genomics platforms and return results to treating oncologist. This objective will be accomplished by enrolling patients and obtaining samples for sequencing and banking. The pathologist-interpreted genomic test results will be returned to the treating oncologist.