RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of calcitriol may prevent prostate cancer. It is not yet known whether calcitriol is more effective than observation in preventing prostate cancer.

PURPOSE: This randomized phase II trial is studying how well calcitriol works in preventing prostate cancer in patients with prostatic intraepithelial neoplasia.

Condition	Intervention	Phase
Prostate Cancer Precancerous Condition	Drug: calcitriol  Procedure: biologically based therapies  Procedure: cancer prevention intervention  Procedure: chemoprevention of cancer  Procedure: complementary and alternative therapy  Procedure: dietary intervention  Procedure: nutritional supplementation	Phase II

Further Study Details: 

OBJECTIVES:

• Determine the effects of calcitriol in patients with high-grade prostatic intraepithelial neoplasia.
• Determine the toxicity of this drug in these patients.
• Determine the effect of this drug on prostate specific antigen in these patients.

OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 arms.

• Patients receive oral calcitriol once daily for 8 weeks. Treatment repeats every 8 weeks for 2 courses in the absence of unacceptable toxicity. After completion of course 2 (week 16), patients undergo biopsy. Patients continue to receive calcitriol for up to 3 additional weeks while the biopsy is being evaluated. Patients with persistent high-grade prostatic intraepithelial neoplasia (HGPIN) by biopsy receive 2 additional courses of calcitriol. Patients with no HGPIN or prostate cancer by biopsy are removed from the study.
• Arm II: Patients undergo observation for 16 weeks. At week 16, patients undergo biopsy. Patients with persistent HGPIN by biopsy receive 2 courses of calcitriol as in arm I. Patients with no HGPIN or prostate cancer by biopsy are removed from the study. After completion of study treatment, patients are followed annually for 2 years.

PROJECTED ACCRUAL: A total of 50 patients (25 per arm) will be accrued for this study.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed high-grade prostatic intraepithelial neoplasia
• Diagnosed within the past 6 months
• No evidence of prostate cancer within the past 6 months
• No evidence of palpable nodules on digital rectal exam
• Prostate specific antigen ≤ 10 ng/mL within the past 3 months

PATIENT CHARACTERISTICS: Age

• 18 and over

Performance status

• ECOG 0-1

Life expectancy

• Not specified

Hematopoietic

• Absolute neutrophil count ≥ 1,500/mm^3
• Platelet count ≥ 100,000/mm^3

Hepatic

• SGOT and SGPT ≤ 1.5 times upper limit of normal

Renal

• No uncontrolled renal failure
• No cancer-related hypercalcemia or kidney stones within the past 5 years

Cardiovascular

• No uncontrolled coronary artery disease
• No uncontrolled congestive heart failure

Other

• Prior malignancy allowed provided patient was curatively treated and has been disease-free for an appropriate time period for the specific cancer
• No known HIV positivity
• No active infection
• No major depression or suicidal ideation
• No other condition that would preclude study compliance
• No other uncontrolled medical condition

PRIOR CONCURRENT THERAPY: Biologic therapy

• Not specified

Chemotherapy

• No prior chemotherapy for any malignancy

Endocrine therapy

• At least 2 weeks since prior and no concurrent finasteride (Prosear® or Propecia®) or other androgen suppressor
• No concurrent corticosteroids

Radiotherapy

• Not specified

Surgery

• Not specified

Other

• At least 2 weeks since prior phenytoin or phenobarbital
• At least 2 weeks since prior ketoconazole
• No concurrent administration of any of the following:
• Magnesium-containing antacids
• Thiazide diuretics
• Calcium supplements
• Digoxin
• Herbal supplements
• Pharmacological doses of cholecalciferol (vitamin D) or its derivatives

Please refer to this study by ClinicalTrials.gov identifier  NCT00118066

New Jersey
      Cancer Center at the Mountainside Hospital, Montclair,  New Jersey,  07042,  United States; Recruiting
      Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School, New Brunswick,  New Jersey,  08903,  United States; Recruiting
      Carol G. Simon Cancer Center at Morristown Memorial Hospital, Morristown,  New Jersey,  07962,  United States; Recruiting
      Central Jersey Oncology Center - East Brunswick, East Brunswick,  New Jersey,  08816,  United States; Recruiting
      Overlook Hospital, Summit,  New Jersey,  07902-0220,  United States; Recruiting

Study chairs or principal investigators

Robert S. DiPaola, MD,  Principal Investigator,  Cancer Institute of New Jersey   

Study ID Numbers:  CDR0000433508; CINJ-080404; CINJ-4901; CINJ-NJ3803; CINJ-5111; NCT00118066
Record last reviewed:  June 2005
Last Updated:  July 25, 2005
Record first received:  July 8, 2005
ClinicalTrials.gov Identifier:  NCT00118066
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-07-26