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Effect of Epidermal Growth Factor Receptor Inhibitors on Magnesium Homeostasis in Patients With Cancer

Terminated
Conditions
Solid Tumor
Registration Number
NCT00898027
Lead Sponsor
Vanderbilt-Ingram Cancer Center
Brief Summary

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.

Detailed Description

OBJECTIVES:

* Determine the effects of EGFR inhibitors on magnesium homeostasis in patients with cancer.

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.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Diagnosis of malignancy

    • Planning to receive therapy with an inhibitor of the EGFR pathway (either on or off a clinical trial and may be monotherapy or combined with other therapies)
  • Normal serum magnesium level

Exclusion Criteria
  • Glomerular filtration rate ≥ 60 mL/min
  • No severe underlying renal dysfunction
  • Normal serum potassium and calcium level
  • No history of primary or secondary hyperparathyroidism

PRIOR CONCURRENT THERAPY:

  • No prior EGFR pathway inhibitor

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Effects of EGFR inhibitors on magnesium homeostasis8 weeks
Secondary Outcome Measures
NameTimeMethod
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