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Clinical Trials/NCT01169363
NCT01169363CompletedNot Applicable

Validation of AML Proteomic Signature Associated With Clinical Response to Ara-C Based Induction Therapy in Patients 60 Years of Age or Older Using Samples From ECOG Studies 3999, 3993 and 1490

ECOG-ACRIN Cancer Research Group0 sites200 target enrollmentStarted: July 8, 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Primary Endpoint
Proportion of patients achieving a complete response to induction chemotherapy

Study Overview

Brief Summary

RATIONALE: Studying samples of bone marrow and blood from patients with cancer in the laboratory may help doctors predict how well patients will respond to treatment.

PURPOSE: This research study is studying biomarkers in bone marrow and blood samples from older patients with acute myeloid leukemia treated with cytarabine-based therapy.

Detailed Description

OBJECTIVES:

Primary

  • To validate a pre-specified proteomic classifier to predict the likelihood of complete response (CR) to cytarabine-based induction chemotherapy in older patients with non-M3 acute myeloid leukemia.

Secondary

  • To identify signaling nodes associated with risk of relapse among these patients who achieve a CR to induction chemotherapy.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Retrospective

Eligibility Criteria

Ages
60 Years to 120 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Proportion of patients achieving a complete response to induction chemotherapy

Time Frame: 1 month

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
ECOG-ACRIN Cancer Research Group
Sponsor Class
Network
Responsible Party
Sponsor

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