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| ID | Type | Description | Link |
|---|---|---|---|
| SU-09232008-1302 | Other Identifier | Stanford University | |
| BRSADJ0014 | Other Identifier | OnCore |
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Low accrual
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| Name | Class |
|---|---|
| United States Department of Defense | FED |
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Aromatase inhibitors are potent suppressors of breast cancer growth, but side effects include bone loss, fractures, arthralgias and myalgias. We hypothesize vitamin D administration might be beneficial in treating these symptoms and to protect bone.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Vitamin D | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Vitamin D | Drug | up to 2400 mg; oral tablet |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Spine Bone Mineral Density T Score Change Over One Year | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Hip Bone Mineral Density (BMD) T-score | one year | |
| Bone Turnover Markers | months 4 and 12 | |
| Arthralgias and Myalgias |
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Inclusion Criteria:
3.1.1 All postmenopausal women with histology-confirmed invasive primary breast cancer, who have completed primary surgical or radiotherapy (XRT) with or without adjuvant chemotherapy and are candidates to receive adjuvant therapy with aromatase inhibitors will be screened for eligibility. Postmenopausal is defined as satisfying one or more of the following criteria: having had bilateral oophorectomy; aged more than 60 years; or aged 55-59 years with an intact uterus and amenorrheic for at least 12 months; or if amenorrheic for less than 12 months (after receiving hysterectomy, hormone therapy or chemotherapy).
3.1.2 At the time of study enrollment, participants will have completed primary surgical or XRT with or without adjuvant chemotherapy. Chemotherapy will be completed at least 28 days prior to enrollment.
3.1.4 Participants will be women between 18-85 years of age. Women and minorities will be actively recruited. Though breast cancer extremely rarely occurs in children and men, this study will only recruit adult females.
3.1.5 Participants will have a life expectancy of at least 5 years.
3.1.6 Participants will have Eastern Clinical Oncology Group (ECOG) performance status 0-2.
3.1.7 Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
3.2.1 Medications affecting bone metabolism (bisphosphonates, anticonvulsants, chronic heparin therapy, chronic glucocorticoid use > 5 mg/day prednisone or equivalent, teriparatide).
3.2.2 Use of any investigational drug within past 90 days.
3.2.3 Metastatic breast cancer. High risk for osteoporosis/fractures (BMD < -2.0, history of non-traumatic fracture). Hyperparathyroidism Hypercalcemia Hypercalciuria (fasting spot urine calcium/creatinine ratio >0.20) History of renal stones Renal failure with creatinine over 2.0
3.2.4 Considering that vitamin D3 is produced by the human body, allergy to vitamin D3 is not expected to develop. Subjects with known history of allergic reaction to compounds used to manufacture capsules (rice powder) will be excluded form this study.
3.2.5 Recent history of excessive alcohol or drug use.
3.2.6 As this study will recruit post-menopausal patients, thus pregnant or nursing patients are not part of this investigation.
3.2.8 This study is designed to study women after completing primary therapy for breast cancer. Survivors of previous cancers and HIV-positive subjects will not be excluded.
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| Name | Affiliation | Role |
|---|---|---|
| Eva Balint | Stanford University | Principal Investigator |
| Robert W Carlson | Stanford University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Stanford University School of Medicine | Stanford | California | 94305 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Vitamin D |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Vitamin D |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Spine Bone Mineral Density T Score Change Over One Year | Data are not accessible. | Posted | 1 year |
|
|
1 year
Adverse event data are not accessible.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Vitamin D | Vitamin D: up to 2400 mg; oral tablet |
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Early termination secondary to low accrual.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Mark D Pegram, MD | Stanford Cancer Institute, Stanford University | 650-723-5801 | mpegram@stanford.edu |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| D001847 | Bone Diseases |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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| ID | Term |
|---|---|
| D014807 | Vitamin D |
| ID | Term |
|---|---|
| D012632 | Secosteroids |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
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| every 4 months |
| Serum Calcium and Fasting Spot Urine Calcium/Creatinine Ratio | every 4 months |
| Participants |
|
| Gender | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Secondary | Change in Hip Bone Mineral Density (BMD) T-score | Data are not accessible. | Posted | one year |
|
|
| Secondary | Bone Turnover Markers | Data are not accessible. | Posted | months 4 and 12 |
|
|
| Secondary | Arthralgias and Myalgias | Data are not accessible. | Posted | every 4 months |
|
|
| Secondary | Serum Calcium and Fasting Spot Urine Calcium/Creatinine Ratio | Data are not accessible. | Posted | every 4 months |
|
|
| 0 |
| 8 |
| 0 |
| 8 |
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| D017437 |
| Skin and Connective Tissue Diseases |
| D009140 | Musculoskeletal Diseases |