An Observational Trial of the Effect of Pharmacogenomics Differences in Phase I and II Metabolism of Tamoxifen on Efficacy and Toxicity
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| City: |
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Hershey |
| State: |
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Pennsylvania |
| Zip Code: |
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17033 |
| Conditions: |
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Breast Cancer - Ductal Carcinoma in Situ |
| Purpose: |
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This study will be an open-label prospective observational trial designed to test
associations between polymorphisms of candidate genes and tamoxifen. Pre- and
post-menopausal women taking tamoxifen as standard therapy or chemopreventive therapy will
be included in this study.
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| Study Summary: |
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This study will be an open-label prospective observational trial designed to test
associations between polymorphisms of candidate genes (focusing initially on the UGT2B7
enzyme) and tamoxifen (TAM) toxicity. Pre- & post-menopausal women (aged ≥18 years) taking
TAM (20 mg/day) as standard therapy or chemopreventive therapy will be included in this
study. Patients will be enrolled after they complete all primary surgery, radiation, and
adjuvant chemotherapy. Patients will be excluded if they are undergoing other adjuvant
endocrine therapies. Other reasons for exclusion will include patients who are pregnant or
lactating, or are currently on corticosteroids, phenobarbital, or megestrol acetate. The
goal will be to recruit a total of 45 eligible patients over a 1 year accrual period. The
investigators expect to treat ~50 new patients per year with TAM at the standard dose of 20
mg/day.
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| Criteria: |
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Inclusion Criteria:
- Patients receiving tamoxifen for adjuvant therapy of breast cancer or ductal
carcinoma in situ, or as chemoprevention
- Age 18 years and above
- May be pre- and post-menopausal
- Females
- Patients may be at any point in their hormonal treatment, but must have completed any
planned surgery, radiation and chemotherapy
- Must use a reliable form of birth control
Exclusion Criteria:
- Pregnant
- Breastfeeding
- Concurrent use of corticosteroids, megestrol, or phenobarbital
- History of allergy to tamoxifen
- Unwilling to have a yearly gynecological exam
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| NCT ID: |
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NCT00886535 |
| Primary Contact: |
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Principal Investigator Leah Cream, MD Penn State Hershey Cancer Institute
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| Backup Contact: |
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N/A |
| Location Contact: |
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Hershey, Pennsylvania 17033 United States
Leah Cream, MD Phone: 717-531-8678 Email: lcream@hmc.psu.edu
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 19, 2013 |
| Modifications to this listing: |
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