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

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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.

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.

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
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200 Hawkins Drive
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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Iowa City, IA
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601 Elmwood Avenue
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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Rochester, NY
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Madison, Wisconsin 53715
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8800 W. Doyne Avenue
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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Milwaukee, WI
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