Status:

COMPLETED

Gene Expression in Tissue From Patients With Acute Lymphoblastic Leukemia

Lead Sponsor:

ECOG-ACRIN Cancer Research Group

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Leukemia

Eligibility:

All Genders

15-65 years

Brief Summary

RATIONALE: Studying the genes expressed in samples of tumor tissue from patients with cancer may help doctors identify biomarkers related to cancer. PURPOSE: This laboratory study is looking at gene ...

Detailed Description

OBJECTIVES: * Identify genes involved in specific biologic processes or molecular functions that contribute to the mechanisms by which the BCR/ABL tyrosine kinase induces a leukemic phenotype using R...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Confirmed diagnosis of acute lymphoblastic leukemia
  • Tissue banked on protocol ECOG-2993 meeting the following criteria:
  • Leukemic blast cell population immunophenotyped in detail (e.g., including CD25) in ECOG's Immunophenotyping Reference Laboratory
  • Flow cytometric analysis of gated blast cells reveals association with the B-cell lineage
  • Mononuclear cell fraction used for RNA isolation contains 75-99% blasts (median 85%)
  • Negative for TEL/AML1, MLL/AF4, and E2A/PBX1 by qualitative reverse transcription-polymerase chain reaction (RT-PCR)
  • No FLT3 gene mutations
  • BCR/ABL-positive samples meeting the following criteria:
  • Presence of t(9;22)(q34;q11) by standard cytogenetics
  • Detection of either p190 BCR/ABL or p210 BCR/ABL transcripts by qualitative RT-PCR
  • Patients with genetic risk factors must meet the following criterion:
  • Only a normal diploid karyotype is present in ≥ 15 metaphases by standard cytogenetics
  • PATIENT CHARACTERISTICS:
  • Not specified
  • PRIOR CONCURRENT THERAPY:
  • Not specified

Exclusion

    Key Trial Info

    Start Date :

    October 26 2007

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    July 19 2012

    Estimated Enrollment :

    137 Patients enrolled

    Trial Details

    Trial ID

    NCT00898261

    Start Date

    October 26 2007

    End Date

    July 19 2012

    Last Update

    May 19 2017

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