Doxercalciferol Before Surgery in Treating Localized Prostate Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Prostate Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 21 - 120 |
Updated: | 4/21/2016 |
Start Date: | August 2001 |
Phase II Open Label, Multi-Center Clinical Trial Of Modulation Of Intermediate Endpoint Biomarkers By 1x-Hydroxyvitamin D2 In Patients With Clinically Localized Prostate Cancer And High Grade PIN
RATIONALE: Doxercalciferol may be an effective way to treat localized prostate cancer before
surgery.
PURPOSE: Randomized phase II trial to study the effectiveness of giving doxercalciferol
before surgery in treating patients who have localized prostate cancer.
surgery.
PURPOSE: Randomized phase II trial to study the effectiveness of giving doxercalciferol
before surgery in treating patients who have localized prostate cancer.
OBJECTIVES:
- Determine whether doxercalciferol modulates intermediate endpoint biomarkers in the
development of prostate cancer in patients with localized prostate cancer.
- Assess the toxicity of this drug in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are randomized to one
of 2 arms.
- Arm I: Patients receive doxercalciferol once daily for 28 days. Patients then undergo
prostatectomy.
- Arm II: Patients undergo observation for 28 days. Patients then undergo prostatectomy.
PROJECTED ACCRUAL: A total of 60 patients (30 per arm) will be accrued for this study within
18 months.
- Determine whether doxercalciferol modulates intermediate endpoint biomarkers in the
development of prostate cancer in patients with localized prostate cancer.
- Assess the toxicity of this drug in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are randomized to one
of 2 arms.
- Arm I: Patients receive doxercalciferol once daily for 28 days. Patients then undergo
prostatectomy.
- Arm II: Patients undergo observation for 28 days. Patients then undergo prostatectomy.
PROJECTED ACCRUAL: A total of 60 patients (30 per arm) will be accrued for this study within
18 months.
DISEASE CHARACTERISTICS:
- Histologically or cytologically confirmed localized adenocarcinoma of the prostate
- Candidate for prostatectomy
PATIENT CHARACTERISTICS:
Age:
- 21 and over
Performance status:
- Not specified
Life expectancy:
- Not specified
Hematopoietic:
- WBC at least 4,000/mm^3
- Platelet count at least 100,000/mm^3
Hepatic:
- Bilirubin no greater than 1.4 mg/dL
- AST no greater than 3 times normal
Renal:
- Creatinine no greater than 2.0 mg/dL
- Calcium no greater than 10.2 mg/dL
- No idiopathic urinary calcium stone disease
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- Not specified
Endocrine therapy:
- No prior hormonal therapy for prostate cancer
- No concurrent hormonal therapy, including luteinizing hormone-releasing hormone
agonists, antiandrogens, glucocorticoids, ketoconazole, finasteride,
diethylstilbestrol, or progestins
Radiotherapy:
- No prior brachytherapy or external beam radiotherapy for prostate cancer
Surgery:
- See Disease Characteristics
Other:
- At least 7 days since prior vitamin D therapy or calcium supplements
- No other concurrent vitamin D analogues or calcium supplements
- No concurrent magnesium-containing antacids
- No concurrent thiazide-containing diuretics
- No concurrent phenytoin, phenobarbital, glutethimide, digoxin, or digitalis
We found this trial at
6
sites
200 Hawkins Drive
Iowa City, Iowa 52242
Iowa City, Iowa 52242
800-237-1225
Holden Comprehensive Cancer Center at University of Iowa Holden Comprehensive Cancer Center is dedicated to...
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601 Elmwood Avenue
Rochester, New York 14642
Rochester, New York 14642
(585) 275-5830
James P. Wilmot Cancer Center at University of Rochester Medical Center The Wilmot Cancer Center...
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8800 W. Doyne Avenue
Milwaukee, Wisconsin 53226
Milwaukee, Wisconsin 53226
(414) 805-6840
Medical College of Wisconsin Cancer Center Cancer touches everyone in our community, and for many,...
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