Studying Tissue and Blood Samples From Patients With Acute Myeloid Leukemia



Status:Active, not recruiting
Conditions:Blood Cancer, Hematology, Leukemia
Therapuetic Areas:Hematology, Oncology
Healthy:No
Age Range:Any
Updated:8/9/2017
Start Date:June 2008

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Assessment of Novel Molecular Markers in Acute Myeloid Leukemia

RATIONALE: Studying samples of tissue and blood 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 research study is looking at tissue and blood samples from patients with acute
myeloid leukemia.

OBJECTIVES:

- Prospectively obtain specimens required for diagnostic review and molecular
characterization ensuring eligibility for CALGB Leukemia Committee Clinical trials (for
clinical trials designed to enroll specific molecular subtypes, results to determine
eligibility will be reported to treating physicians no more than 72 hours after specimen
receipt at the repository).

- Determine the frequency of specific gene markers (i.e., FLT3 ITD, CBF, MLL PTD, NPM1,
KIT, RAS, CEBPA, WT1, JAK2, RUNX1, TET2, CBL, IDH1 and IDH2, ASXL1, mutations, aberrant
BAALC, ERG, FLT3, MN1, EVI1, and APP) over-expression and levels of promoter methylation
of specific genes (e.g., ESR1, WIT1, P15, MYOD1, ID4, DPK) in defined cytogenetic
subgroups of patients with acute myeloid leukemia (AML).

- Correlate these gene markers with clinical and laboratory parameters in these patients.

- Correlate these gene markers with clinical outcome (i.e., complete remission [CR],
disease-free survival [DFS], cumulative incidence of relapse [CIR], and overall survival
[OS]) in these patients.

- Identify specific microarray multi-gene expression signatures in these patients.

- Correlate specific microarray multi-gene expression signatures with clinical and
laboratory parameters in these patients.

- Correlate specific microarray multi-gene expression signatures with clinical outcome
(i.e., CR, DFS, CIR, and OS) in these patients.

- Identify specific microarray multi-microRNA (miR) expression signatures in these
patients

- Correlate specific microarray multi-miR expression signatures with clinical and
laboratory parameters in these patients.

- Correlate specific microarray multi-miR expression signatures with clinical outcome
(i.e., CR, DFS, CIR, and OS) in these patients.

- Explore the relative contribution of prognostic gene markers (i.e., FLT3 ITD, MLL PTD,
NPM1, KIT, RAS, CEBPA, WT1, and JAK2 mutations, and aberrant BAALC, ERG, FLT3, MN1, and
EVI1 over-expression), levels of promoter methylation of specific genes (e.g., ESR1,
WIT1, P15, MYOD1, ID4, DPK), and microarray gene and miR expression signatures in
defined cytogenetic subgroups of AML.

- Determine changes in these molecular markers and microarray gene and miR expression
signatures at CR and relapse and the influence that these changes have on subsequent
clinical course.

- Correlate the relative level of nuclear pSTAT5 and pERK in bone marrow blasts with
outcome (EFS, CR, DFS, OS).

OUTLINE: This is a multicenter study.

Previously procured and archived bone marrow aspirate samples, blood and buccal cell samples,
and bone marrow biopsy slides are analyzed for FLT3 ITD, MLL PTD, NPM1, KIT, KRAS, NRAS,
CEBPA, WT1, JAK2, RUNX1, TET2, ASXL1, IDH1 and IDH2, and CBL mutations, CBF fusion genes,
levels of BAALC, ERG, EVI1, MN1, and APP microarray gene-expression, microRNA gene-expression
signature, levels of methylation of genes silenced in AML, and genomic DNA by PCR
amplification, RT-PCR, and denaturing high-performance liquid chromatography.

DISEASE CHARACTERISTICS:

- Histologically confirmed acute myeloid leukemia (AML)

- Tissue samples from previously untreated patients with AML considered for enrollment
onto ongoing and future CALGB treatment protocols

- AML tissue samples from companion Leukemia Tissue Bank protocol CALGB-9665 and the
companion cytogenetic protocol CALGB-8461

- AML diagnostic bone marrow and/or blood samples from patients enrolled on CLB-9720,
CLB-9621 (all cytogenetic subtypes), and CALGB-19808 (abnormal cytogenetics only)
We found this trial at
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1304 Franklin Avenue
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361 Old Belgrade Road
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417 State St #30
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185 Cambridge Street
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666 Elm Street
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200 Hawthorne Lane
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115 Business loop 70 w
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11143 Parkview Plaza Dr # 100
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600 Moye Boulevard
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200 Hawkins Drive
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701 Doctors Dr
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One Medical Center Drive
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902 Savannah Road
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2501 N Orange Ave # 235
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Richmond, Virginia 23298
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750 E Adams St
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42 E Laurel Rd # 2545
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1 Medical Center Blvd
Winston-Salem, North Carolina 27103
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300 North Ave
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130 Fisher Road
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1505 Eastland Drive
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44 Binney St
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210 W Walnut St
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101 Manning Drive
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1801 West Taylor, Suite 1E
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2650 Ridge Ave.
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3315 N. Seminary Street
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250 Cherry St SE
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520 E. Franklin
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800 N Justice St
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205 Tenney St
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1700 Oak Ave.
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4701 Ogletown-Stanton Road
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603 S 13th St
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530 NE Glen Oak Ave
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925 West St
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300 N Patterson Rd
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