View Clinical Trial (Medical Research Study)
Understanding the Role of Adherence in the Ethnic Differences in Survival After Childhood ALL
| City: |
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Indianapolis |
| State: |
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Indiana |
| Zip Code: |
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46202 |
| Conditions: |
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Leukemia |
| Purpose: |
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RATIONALE: Assessing why young patients who have acute lymphoblastic leukemia may not take
their medications as prescribed may help identify ways to assist them in taking their
medications more consistently and may improve long-term treatment outcomes.
PURPOSE: This clinical trial is assessing compliance with long-term mercaptopurine treatment
in young patients with acute lymphoblastic leukemia in remission.
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| Study Summary: |
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OBJECTIVES:
Primary
- Determine and compare adherence to maintenance mercaptopurine using the following
assessments: serial red cell mercaptopurine metabolites (i.e., 6TGN and methylTIMP),
frequency of mercaptopurine dosing using an electronic pill monitoring system (MEMS^®),
and self-report of adherence to mercaptopurine by questionnaire in a cohort of younger
patients with acute lymphoblastic leukemia in first remission who belong to four
different ethnic and racial groups (Caucasians, African-Americans, Hispanics, and
Asians).
- Determine the impact of adherence to mercaptopurine on event-free-survival (EFS) in the
entire cohort, after adjusting for known predictors of disease outcome.
- Define a critical level of adherence that has a significant impact on EFS for the
entire cohort.
- Describe prevalence of adherence to mercaptopurine by ethnicity.
- Describe behavioral and sociodemographic predictors of adherence.
- Describe the pill-taking practices in this cohort.
- Evaluate the impact of adherence on ethnic/racial difference in EFS.
Secondary
- Assess the concordance among 6TGN and methylTIMP levels, electronic pill monitoring,
and self-reported adherence in the ethnic/racial groups.
OUTLINE: This is a multicenter study.
Patients* receive an electronic pill monitoring system comprising an empty MEMS^® medication
bottle with TrackCap™ child resistant (CR). The mercaptopurine prescription is filled using
this system. Beginning on day 1 of the third or later course of maintenance therapy,
patients take all doses of mercaptopurine from the MEMS^® medication bottle with TrackCap™
CR for at least 6 months. The MEMS^® TrackCap™ CR is mailed to the study center at the end
of study. Patients also receive oral methotrexate as indicated by their individual
chemotherapy regimen.
NOTE: *Study closed to accrual for Caucasian and Hispanic patients as of 8/14/2009.
Blood samples are collected on days 1, 29, 57, 85, 113, 141, and 169. Patient or caregiver
completes demographic questionnaire on day 29. Patient and/or caregiver completes a
self-reported adherence questionnaire on days 29, 57, 113, and 141.
After completion of study treatment, patients are followed periodically.
PROJECTED ACCRUAL: A total of 720 patients will be accrued for this study.
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| Criteria: |
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DISEASE CHARACTERISTICS:
- Diagnosis of acute lymphoblastic leukemia (ALL) at ≤ 21 years of age
- Disease in first remission
- Receiving self- or parent/caregiver-administered oral antimetabolite chemotherapy
during the maintenance phase of therapy
- Has completed at least two courses* of maintenance chemotherapy, and is
scheduled to receive at least two more planned courses of maintenance
chemotherapy NOTE: *A course is defined as 12 weeks/84 days of maintenance
chemotherapy.
- Treatment plan must include oral mercaptopurine (6-MP) at 75 mg/m^2/day and
oral methotrexate at 20 mg/m^2/week during the maintenance phase
- Dose modification of 6-MP or methotrexate based on laboratory or
clinical parameters is acceptable
PATIENT CHARACTERISTICS:
- Belongs to one of the four following ethnic/racial categories: African-American,
Asian, Caucasian*, or Hispanic* NOTE: Closed to accrual for Caucasian and Hispanic
patients as of 8/14/2009.
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- Concurrent enrollment on another therapeutic study for ALL allowed
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| NCT ID: |
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NCT00268528 |
| Primary Contact: |
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Study Chair
Smita Bhatia, MD, MPH
Beckman Research Institute
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| Backup Contact: |
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N/A |
| Location Contact: |
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Indianapolis, Indiana 46202
United States
Clinical Trials Office - Indiana University Cancer Center
Phone: 317-274-2552
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 25, 2013 |
| Modifications to this listing: |
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