Oral selenium supplementation has no effect on prostate-specific antigen velocity in men undergoing active surveillance for localized prostate cancer.
Oral selenium supplementation has no effect on prostate-specific antigen velocity in men undergoing active surveillance for localized prostate cancer.
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DOI:
10.1158/1940-6207.capr-09-0143
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发表时间:
2010-08
期刊:
影响因子:
--
通讯作者:
Ahmann FR
中科院分区:
文献类型:
--
作者:
Stratton MS;Algotar AM;Ranger-Moore J;Stratton SP;Slate EH;Hsu CH;Thompson PA;Clark LC;Ahmann FR
The Nutritional Prevention of Cancer Trial demonstrated a 52% lower incidence of prostate cancer in men supplemented with selenium. As a result, our study was designed to assess whether selenium supplementation attenuates the progression of prostate cancer. A Phase 2 randomized, double-blind, placebo-controlled clinical trial was conducted in men with localized non-metastatic prostate cancer who had elected to forgo active treatment and be followed by active surveillance. A total of 140 men were randomized to placebo (n=46), 200 μg/day (n=47) or 800 μg/day (n=47) selenium p.o. (as selenized yeast) and followed every 3 months for up to 5 years. PSA velocity was used as a marker of prostate cancer progression and was estimated using mixed effects regression. Adjusting for age, body mass index, baseline selenium, smoking, baseline PSA, race, PSA method, and Gleason score; PSA velocities for 200 μg/day and 800 μg/day treatment groups were not statistically significantly different from placebo (p = 0.32 and p = 0.61 respectively). In the highest quartile of baseline selenium, men supplemented with 800 μg selenium demonstrated PSA velocity statistically significantly higher as compared to placebo (p = 0.018). Selenium supplementation did not show a protective effect on PSA velocity in subjects with localized prostate cancer. On the contrary, supplementation with high dose selenium was observed to be a risk factor for increased PSA velocity in men with high baseline plasma selenium concentrations. clinicaltrials.gov (NCT00752739)