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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01145469
Other study ID # CDR0000674957
Secondary ID ECOG-E2997T2
Status Completed
Phase N/A
First received June 15, 2010
Last updated May 16, 2017
Start date June 1, 2010
Est. completion date August 1, 2010

Study information

Verified date May 2017
Source Eastern Cooperative Oncology Group
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

RATIONALE: Studying samples of DNA in the laboratory from patients who received fludarabine-based treatment may help doctors learn more about the effects of fludarabine on cells. It may also help doctors understand how well patients respond to treatment.

PURPOSE: This research study is studying DNA samples from patients with chronic lymphocytic leukemia previously treated with fludarabine-based therapy.


Description:

OBJECTIVES:

- To identify genetic characteristics associated with the efficacy and toxicity of fludarabine-based treatment in patients with chronic lymphocytic leukemia who participated on E2997.

- To validate these genetic characteristics with a cancer cell model system to confirm association and dissect the mechanism of effect.

OUTLINE: Archived DNA samples are analyzed for genetic characteristics associated with the efficacy and toxicity to fludarabine-based treatment using Affymetrix 6.0 single nucleotide polymorphism arrays. The results are then compared with data of genes identified in a cancer cell model system, and with clinical data (response, toxicity, overall survival, and progression-free survival) associated with each patient sample.


Recruitment information / eligibility

Status Completed
Enrollment 225
Est. completion date August 1, 2010
Est. primary completion date August 1, 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years to 120 Years
Eligibility DISEASE CHARACTERISTICS:

- Diagnosis of chronic lymphocytic leukemia

- Archived DNA samples

- Received fludarabine with versus without cyclophosphamide on clinical trial E2997

PATIENT CHARACTERISTICS:

- Not specified

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
DNA analysis

gene expression analysis

polymorphism analysis

Other:
laboratory biomarker analysis

medical chart review


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Eastern Cooperative Oncology Group National Cancer Institute (NCI)

Outcome

Type Measure Description Time frame Safety issue
Primary Association of single SNP genotype with overall and progression-free survival 1 month
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