Selenium in Preventing Prostate Cancer

University of Arizona

Status and phase: Completed; Phase 3

Conditions: Prostate Cancer

Treatments: Other: placebo; Dietary Supplement: high-selenium baker's yeast; Dietary Supplement: selenium

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00978718

R01CA077789 (U.S. NIH Grant/Contract)

P30CA023074 (U.S. NIH Grant/Contract)

UARIZ-99-0045-01, (Other Identifier)

01-0506-01

Details and patient eligibility

About

RATIONALE: Selenium supplements may stop or delay the development of prostate cancer in patients at high risk of prostate cancer. It is not yet known which dose of selenium may be more effective in preventing prostate cancer.

PURPOSE: This randomized phase III trial is studying how well selenium works in preventing prostate cancer.

Full description

OBJECTIVES:

• To determine whether selenium (Se) supplementation decreases the incidence of prostate cancer.
• To determine whether Se supplementation inhibits the biochemical progression of prostate cancer.

OUTLINE: This is a multicenter study. Patients are randomized to 1 of 3 treatment arms.

• Arm I: Patients receive oral placebo daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.
• Arm II: Patients receive 200 μg of oral selenium (Se) as high-Se Baker's yeast daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.
• Arm III: Patients receive 400 μg of oral Se as high-Se baker's yeast daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.

Blood samples are collected at baseline, at randomization, and then semi-annually for laboratory and other testing. Tissue samples may also be collected for biomarker analysis. Patients complete an initial questionnaire and urological-symptoms questionnaire at baseline, a follow-up questionnaire after randomization (to capture new illness, medications, and toxicity symptoms during the 30-day run-in period; a urological-symptoms questionnaire; a food-frequency questionnaire; and a mood questionnaire). Patients then undergo questionnaires semi-annually, including vital status, tablet compliance, nutrition, mood, new illnesses or medications, and any incidence of cancer or family history of cancer).

Enrollment: 700 estimated patients

Sex: Male

Ages: Under 79 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Clinical indicators consistent with the community standards of medical care that would justify a biopsy of the prostate for the diagnosis of cancer, including ≥ 1 of the following:

  • PSA level above the absolute value of 4 ng/mL or above a published age-ethnic adjusted PSA level appropriate for the community
  • Rising PSA that should represent a clinically significant PSA velocity (e.g., an estimated annual change in the PSA velocity ≥ 0.75 ng/mL)
  • Abnormal digital rectal examination of the prostate that identifies a clinically significant change in the prostate (e.g., a prostate nodule or a change in the firmness of the prostate)
  • Documentation of the clinical assessment that justified the prostate biopsy that allows classification of the patient to high-risk groups

• Prostate biopsy negative for cancer within the past 12 months

• Prostate biopsy negative for high-grade prostatic intraepithelial neoplasia (PIN)

  • PIN allowed provided it is grade 1

PATIENT CHARACTERISTICS:

• Creatinine < 2 times upper limit of normal (ULN)

• Bilirubin < 2 times ULN

• SGOT and SGPT < 2 times ULN

• Alkaline phosphatase < 2 times ULN

• No history of a prior malignancy except for the following:

  • Adequately treated basal cell or squamous cell carcinoma
  • Adequately treated (i.e., complete surgical removal with negative margins) stage I cancer from which the patient is currently in complete remission
  • Any other cancer from which the patient has been disease-free for 5 years

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No prior systemic chemotherapy or radiotherapy
• At least 90 days since prior and no other concurrent selenium > 55 μg/day as a dietary supplement (including multivitamin supplements)
• More than 30 days since prior and no concurrent participation in any other clinical trial involving a medical, surgical, nutritional, or life-style intervention (e.g., dietary modifications, exercise)

Trial design

700 participants in 3 patient groups, including a placebo group

Arm I

Placebo Comparator group

Description:

Patients receive oral placebo daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.

Treatment:

Other: placebo

Arm II: 200 μg selenium (Se) as high-Se Baker's yeast daily

Experimental group

Description:

Patients receive 200 μg of oral selenium (Se) as high-Se Baker's yeast daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.

Treatment:

Dietary Supplement: selenium

Arm III: 400 μg Se as high-Se baker's yeast daily

Experimental group

Description:

Patients receive 400 μg of oral Se as high-Se baker's yeast daily. Treatment continues for up to 57 months in the absence of unacceptable toxicity or diagnosis of prostate cancer.

Treatment:

Dietary Supplement: high-selenium baker's yeast