HomeAbout SPIFor PatientsFor PhysiciansSPI DoctorsDirections206.215.2480

Clinical Training CoursesTechnical AssistanceBrachytherapy ConferencePCa Commentary



PCa Commentary

Selenium (March 2006)

It’s going to be long wait until 2012 when the results become available from the large SELECT trial evaluating possible benefit for selenium (Se) and Vitamin E in prostate cancer prevention. However for impatient persons, currently it could be considered a “good bet” that the intake of 200 mcg. of selenium confers benefit in lowering the risk and aggressiveness of prostate cancer. In vitro evidence suggests that selenium is anticarcinogenic by promoting apoptosis, inhibiting angiogenesis and cellular proliferation, and serving as an antioxidant.

However, the strength of evidence is diminished by some important qualifications. The Nutritional Prevention of Cancer Trial (NPCT) compared supplemental 200 mcg Se to placebo, and at 7.4 years of follow-up prostate cancer incidence was reduced by 64%, but only in those men with low baseline Se levels, i.e. <125 ng/mL.

Similar findings were reported from the analysis of the Physicians’ Health Study (PHS), best summarized in the Am. J. of Urol. Rev., Jan 2005. This study was based on 13 year follow-up data of 22,071 healthy male physicians and it evaluated the incidence of prostate cancer in relation to dietary history. A 48% reduction of the risk of advanced, i.e., Stage C and D, cancer was seen, but only was seen in the men in the lowest quintile of baseline Se levels who also had baseline PSA values of > 4 ng/mL. A comparatively high level of selenium was associated with a statistically non-significant 22% reduction in the overall incidence of prostate cancer.

The superior risk reduction seen in the NPCT trial could have resulted from the higher (190 ng/mL) mean level of Se in the NPCT patients achieved by the 200 mcg supplements compared to the mean level of 104 ng/ml seen in the PHS wherein physicians freely chose their diets.
A literature meta-analysis by Canadian researchers (Cancer Causes Control, 2005 Nov) was more generally supportive of benefit for lycopene and found a 26% risk reduction from moderate dietary Se intake (no Se supplementation). They reported that “A dose-response trend was observed when we stratified the studies by disease severity”.

Short of actually measuring the serum or toenail level of Se, an individual would be betting on the side of strongest evidence by taking 200 mcg. Of supplemental Se.

« Back to Article List


(c) 2006 Seattle Prostate Institute -  All rights reserved.