Vitamin D3 (Vit D3) Supplementation and T Cell Immunomodulation in Patients With Newly Diagnosed Operative Invasive Ductal Breast Carcinoma
| Status: | Terminated |
|---|---|
| Conditions: | Breast Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | January 2013 |
| End Date: | November 2014 |
Vitamin D3 (Vit D3) Supplementation and T Cell Immunomodulation in Patients With Newly Diagnosed Operative Invasive Ductal Breast Carcinoma Stage I-II
This study is for adult females who have been newly diagnosed with breast cancer that
includes surgery as part of standard cancer treatment. This is a research study combining
Vitamin D (an over the counter medication) with the standard of care (or the established and
approved treatment), surgery. Evidence shows that women who are Vitamin D3 deficient have a
higher risk of breast cancer and breast cancer recurrence. The purpose of this study is to
find out the effects of Vitamin D3 during the treatment period for Stage I-II breast cancer.
Screening tests will be done to determine if subjects are eligible to participate in this
study. If subjects are eligible and they agree to participate, they will be assigned to one
of two groups which will receive different amounts of vitamin D. Subjects will be asked to
keep a medication diary. Subjects may remain on treatment for approximately 56 days.
includes surgery as part of standard cancer treatment. This is a research study combining
Vitamin D (an over the counter medication) with the standard of care (or the established and
approved treatment), surgery. Evidence shows that women who are Vitamin D3 deficient have a
higher risk of breast cancer and breast cancer recurrence. The purpose of this study is to
find out the effects of Vitamin D3 during the treatment period for Stage I-II breast cancer.
Screening tests will be done to determine if subjects are eligible to participate in this
study. If subjects are eligible and they agree to participate, they will be assigned to one
of two groups which will receive different amounts of vitamin D. Subjects will be asked to
keep a medication diary. Subjects may remain on treatment for approximately 56 days.
Inclusion Criteria:
- Patients must be greater than or equal to 18 years of age.
- Patients must have a newly diagnosed invasive ductal breast carcinoma, Stage I-II.
- Patients who have completed their surgical and radiation therapy.
- Patients must have SWOG performance status of 0, 1 or 2.
- Patients must have adequate organ function as defined by:
- Hgb > 8.0 gm/dl, WBC > 3,500, platelet count > 100,000
- Bilirubin < 2.0 mg/dl, SGOT < 4x upper limit of normal
- Creatinine < 2.0 mg/dl or calculated creatinine clearance > 50 ml/min
- Patients must have a serum calcium - phosphate product that is less than 70.
- Patients must have recovered from any prior surgery.
- Patients must be willing to use appropriate contraception if of child-bearing
potential.
- Patients may be on standard of care maintenance dose Vit D3
Exclusion Criteria:
- Patients with histology of lobular carcinoma.
- Patients with metastatic disease.
- Pregnant or lactating women.
- Male gender.
- Patients with a history of sarcoidosis.
- Patients with any history of idiopathic urinary calcium stone disease, chronic
hypercalcemia, or gastrointestinal malabsorptive conditions.
- Patients who have received any of the following treatments within the last 14 days
prior to study registration will be excluded.
- Lithium
- Digitalis
- Thiazide diuretics
- Calcium supplementation during 1,25-dihydroxyvitamin D3 treatment
- Bisphosphonates
- Teriparatide
- Aluminum Hydroxide
- Bile Acid sequestrants
- Repletion dose VitD3 in setting of known Vit D3 deficiency or insufficiency
- Patients who have received concurrent corticosteroid treatments within the last 14
days prior to study registration will be excluded.
- Known HIV positive.
- Patients with an active infection requiring antibiotic therapy.
- Other malignancies unless the patient is considered to be disease-free for 5 or more
years prior to randomization and is deemed by her physician to be at low risk for
recurrence. Patients with the following cancers are eligible if diagnosed and treated
within the past 5 years: carcinoma in situ of the cervix, carcinoma in situ of the
colon, melanoma in situ, and basal cell and squamous cell carcinoma of the skin.
- Patients undergoing neoadjuvant chemotherapy or neoadjuvant endocrine therapy.
We found this trial at
1
site
171 Ashley Avenue
Charleston, South Carolina 29425
Charleston, South Carolina 29425
843-792-1414
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
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