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Clinical Trials/NCT00897767
NCT00897767
Completed
Not Applicable

Ancillary Laboratory Protocol For the Collection of Diagnostic Material On Patients Considered For ECOG Treatment Trials For Leukemia Or Related Hematologic Disorders

Eastern Cooperative Oncology Group213 sites in 1 country1,873 target enrollmentSeptember 21, 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Leukemia
Sponsor
Eastern Cooperative Oncology Group
Enrollment
1873
Locations
213
Primary Endpoint
Obtaining baseline sample collection for correlative studies outlined in parent clinical trials
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

RATIONALE: Collecting and storing samples of blood and bone marrow from patients with cancer to study in the laboratory may help doctors learn more about diagnosing cancer and determine a patient's eligibility for a treatment clinical trial. It may also help the study of cancer in the future.

PURPOSE: This laboratory study is collecting tissue samples from patients with leukemia or other blood disorders who are planning to enroll in an ECOG leukemia treatment clinical trial.

Detailed Description

OBJECTIVES: * To provide a mechanism for sample collection and submission for diagnostic review to determine eligibility of patients with suspected leukemia or related hematologic disorders for enrollment on ECOG leukemia clinical trials. * To obtain baseline samples for correlative studies outlined in parent clinical trials. OUTLINE: This is a cohort, multicenter study. Patients submit bone marrow and/or blood samples. The samples are studied to determine patients' eligibility for ECOG leukemia treatment clinical trials. Samples may be stored for future correlative studies related to ECOG treatment clinical trials.

Registry
clinicaltrials.gov
Start Date
September 21, 2004
End Date
December 21, 2014
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Obtaining baseline sample collection for correlative studies outlined in parent clinical trials

Time Frame: 6 month

Providing a mechanism for sample collection and submission for diagnostic review to determine eligibility for enrollment on ECOG leukemia clinical trials

Time Frame: 6 month

Study Sites (213)

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