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| ID | Type | Description | Link |
|---|---|---|---|
| VU-VICC-GI-0615 | |||
| VU-VICC-IRB-060364 |
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slow accrual
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
| National Institutes of Health (NIH) | NIH |
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RATIONALE: Studying samples of blood and urine in the laboratory from patients with cancer receiving epidermal growth factor receptor inhibitors may help doctors understand the effect of epidermal growth factor receptor inhibitors on magnesium levels in the body.
PURPOSE: This laboratory study is looking at the effect of epidermal growth factor receptor inhibitors on magnesium homeostasis in patients with cancer.
OBJECTIVES:
OUTLINE: This is a pilot study.
Patients undergo blood and urine sample collection at baseline and at 2, 4, and 8 weeks during treatment.
After finishing treatment, patients are followed periodically for up to 10 weeks.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| laboratory biomarker analysis | Other | laboratory biomarker analysis |
| Measure | Description | Time Frame |
|---|---|---|
| Effects of EGFR inhibitors on magnesium homeostasis | 8 weeks |
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Inclusion Criteria:
Diagnosis of malignancy
Normal serum magnesium level
Exclusion Criteria:
PRIOR CONCURRENT THERAPY:
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Individuals with the diagnosis of a malignancy for which they are considering therapy with an inhibitor of the EGFR pathway, have received an inhibitor of the EGFR pathway prior to study start, have no severe underlying renal dysfunction as defined as estimated GFR<60 by MDRD equation and must be ≥ 18 years of age.
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| Name | Affiliation | Role |
|---|---|---|
| Laura Goff, MD | Vanderbilt-Ingram Cancer Center | Principal Investigator |
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