학술논문

Vitamin E and the Risk of Prostate Cancer: The Selenium and Vitamin E Cancer Prevention Trial (SELECT)
Document Type
article
Source
JAMA. 306(14)
Subject
Clinical Research
Aging
Nutrition
Complementary and Integrative Health
Cancer
Clinical Trials and Supportive Activities
Urologic Diseases
Prostate Cancer
Prevention
3.3 Nutrition and chemoprevention
Evaluation of treatments and therapeutic interventions
Prevention of disease and conditions
and promotion of well-being
6.1 Pharmaceuticals
Aged
Antioxidants
Dietary Supplements
Follow-Up Studies
Humans
Incidence
Male
Middle Aged
Prostatic Neoplasms
Risk
Selenium
Vitamin E
Medical and Health Sciences
General & Internal Medicine
Language
Abstract
ContextThe initial report of the Selenium and Vitamin E Cancer Prevention Trial (SELECT) found no reduction in risk of prostate cancer with either selenium or vitamin E supplements but a statistically nonsignificant increase in prostate cancer risk with vitamin E. Longer follow-up and more prostate cancer events provide further insight into the relationship of vitamin E and prostate cancer.ObjectiveTo determine the long-term effect of vitamin E and selenium on risk of prostate cancer in relatively healthy men.Design, setting, and participantsA total of 35,533 men from 427 study sites in the United States, Canada, and Puerto Rico were randomized between August 22, 2001, and June 24, 2004. Eligibility criteria included a prostate-specific antigen (PSA) of 4.0 ng/mL or less, a digital rectal examination not suspicious for prostate cancer, and age 50 years or older for black men and 55 years or older for all others. The primary analysis included 34,887 men who were randomly assigned to 1 of 4 treatment groups: 8752 to receive selenium; 8737, vitamin E; 8702, both agents, and 8696, placebo. Analysis reflect the final data collected by the study sites on their participants through July 5, 2011.InterventionsOral selenium (200 μg/d from L-selenomethionine) with matched vitamin E placebo, vitamin E (400 IU/d of all rac-α-tocopheryl acetate) with matched selenium placebo, both agents, or both matched placebos for a planned follow-up of a minimum of 7 and maximum of 12 years.Main outcome measuresProstate cancer incidence.ResultsThis report includes 54,464 additional person-years of follow-up and 521 additional cases of prostate cancer since the primary report. Compared with the placebo (referent group) in which 529 men developed prostate cancer, 620 men in the vitamin E group developed prostate cancer (hazard ratio [HR], 1.17; 99% CI, 1.004-1.36, P = .008); as did 575 in the selenium group (HR, 1.09; 99% CI, 0.93-1.27; P = .18), and 555 in the selenium plus vitamin E group (HR, 1.05; 99% CI, 0.89-1.22, P = .46). Compared with placebo, the absolute increase in risk of prostate cancer per 1000 person-years was 1.6 for vitamin E, 0.8 for selenium, and 0.4 for the combination.ConclusionDietary supplementation with vitamin E significantly increased the risk of prostate cancer among healthy men.Trial registrationClinicaltrials.gov Identifier: NCT00006392.