Biomarkers in Bone Marrow Samples From Patients With Acute Myeloid Leukemia

NCT01251159 — Completed, 30 participants, ECOG-ACRIN Cancer Research Group

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Somatic Mutations in Stem and Progenitor Cells in AML

RegistryNCT01251159
StatusCompleted
Study typeObservational
Enrollment30 (Actual)
SponsorECOG-ACRIN Cancer Research Group (Network); collaborators: National Cancer Institute (NCI)
ConditionsLeukemia
Interventionsmutation analysis, polymerase chain reaction, immunologic technique, laboratory biomarker analysis (Genetic, other)
Datesstart 2009-05-15, primary completion 2009-06-15, completion 2009-06-15, first posted 2010-12-01, last updated 2017-05-17

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-Summary

RATIONALE: Studying samples of bone marrow from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.

PURPOSE: This laboratory study is studying bone marrow samples from patients with acute myeloid leukemia.

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+Detailed description

OBJECTIVES:

* To rigorously examine fractionated hematopoietic stem and progenitor cells from patients with acute myeloid leukemia (AML).
* To define somatic mutations occurring in de novo AML, including the FLT3-ITD, CEBPA, NPM1, TET2, ASXL1, IDH1, and IDH2 mutations.
* To examine what cellular compartments (LT-HSC, ST-HSC, CMP, GMP, and MEP) contain the selected mutations and in what order those mutations occur.

OUTLINE: Archived bone marrow specimens are analyzed for sequencing and detection of mutations by Sanger-based resequencing of PCR amplicons. Results are then compared with the results of age-matched healthy controls.

+Arms and interventions

  • mutation analysis (Genetic)
  • polymerase chain reaction (Genetic)
  • immunologic technique (Other)
  • laboratory biomarker analysis (Other)

+Outcome measures

Primary outcomes

  • Define somatic mutations occurring in de novo AML [1 month]

+Eligibility

Sex: All, ages: 16 Years to 60 Years

DISEASE CHARACTERISTICS:

* Diagnosis of acute myeloid leukemia
* Bone marrow samples must meet 1 of the following criteria:

  * Normal karyotype from patients enrolled on ECOG-1900 archived at the ECOG Leukemia Tissue Bank

    * Live, sortable mononuclear cells prepared at the time of initial diagnosis (slow-frozen in media with 10% DMSO OR fresh cells shipped immediately
  * Age-matched healthy control samples from commercial providers

PATIENT CHARACTERISTICS:

* Not specified

PRIOR CONCURRENT THERAPY:

* Not specified

+Investigators