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Cancer Epidemiology Biomarkers & Prevention Vol. 12, 77, January 2003
© 2003 American Association for Cancer Research


Letters to the Editor

Correspondence re: Duffield-Lillico et al. Baseline Characteristics and the Effect of Selenium Supplementation on Cancer Incidence in a Randomized Clinical Trial: A Summary Report of the Nutritional Prevention of Cancer Trial. 11: 630–639, 2002

Marco Vinceti1, Carlotta Malagoli, Margherita Bergomi and Gianfranco Vivoli

Dipartimento di Scienze Igienistiche, Microbiologiche e Biostatistiche, Universitá di Modena e Reggio Emilia, Via Campi 287, 4100 Modena, Italy

Duffield-Lillico et al. (1) recently updated cancer incidence estimates among patients with nonmelanoma skin cancer randomized to receive either 200 µg/die (organic?) selenium as selenized yeast or placebo. They reported that an increase of only 25 months of follow-up attenuated the previously reported reduction in incidence of prostate, colorectal, and lung cancer (2) . This finding is consistent with the hypothesis that a favorable effect of selenium administration, if there is any, is short term. Furthermore, the reduction appears to be confined to males and subjects with the lowest selenium status at baseline. In contrast, there were excesses for some other cancer sites, including breast cancer, melanoma, head and neck cancer, lymphoma and leukaemia, confirming earlier epidemiologic reports (3, 4, 5, 6) . In view of this uncertain benefit, it may be prudent to reserve additional testing (7) to patients with frank cancer. Additional follow-up from this experimental cohort beyond the end of the active intervention (which ended on February 1, 1996) would be of great interest.

Duffield-Lillico et al. (1) also reported an excess cancer risk in selenium-treated patients who had the highest plasma selenium levels at baseline. It would be interesting to know which site-specific cancers showed this relation with baseline selenium levels.

Finally, this trial may offer unique opportunities to examine the possible occurrence of toxic effects of selenium in humans (8 , 9) . Recent clinical and epidemiologic studies indicated that both the possible effects short term (decrease of triiodothyronine synthesis and of natural killer cell activity) and long term (such as motor neurons toxicity) may occur at much low levels of selenium exposure, although the chemical forms of selenium may be a determining factor for these effects (10) . Should biological specimens after the beginning of selenium treatment be available from cohort members and should a follow-up extended to other degenerative diseases such as amyotrophic lateral sclerosis be possible, extensive investigation of the above-mentioned issue would be of great interest.

Footnotes

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 E-mail: marco.vinceti{at}unimore.it Back

Received 9/20/02; revised 9/20/02; accepted 10/31/02.

References

  1. Duffield-Lillico A. J., Reid M. E., Turnbull B. W., Combs G. F., Jr., Slate E. H., Fischbach L. A., Marshall J. R., Clark L. C. Baseline characteristics and the effect of selenium supplementation on cancer incidence in a randomized clinical trial: a summary report of the Nutritional Prevention of Cancer Trial. Cancer Epidemiol. Biomark. Prev., 11: 630-639, 2002.[Abstract/Free Full Text]
  2. Clark L. C., Combs G. F., Jr., Turnbull B. W., Slate E. H., Chalker D. K., Chow J., Davis L. S., Glover R. A., Graham G. F., Gross E. G., Krongrad A., Lesher J. L., Jr., Park H. K., Sanders B. B., Jr., Smith C. L., Taylor J. R. Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin. A randomized controlled trial. Nutritional Prevention of Cancer Study Group. J. Am. Med. Assoc., 276: 1957-1963, 1996.[Abstract]
  3. van Noord P. A., Maas M. J., van der Tweel I., Collette C. Selenium and the risk of postmenopausal breast cancer in the DOM cohort. Breast Cancer Res. Treat., 25: 11-19, 1993.[Medline]
  4. Garland M., Morris J. S., Stampfer M. J., Colditz G. A., Spate V. L., Baskett C. K., Rosner B., Speizer F. E., Willett W. C., Hunter D. J. Prospective study of toenail selenium levels and cancer among women. J. Natl. Cancer Inst. (Bethesda), 87: 497-505, 1995.[Abstract/Free Full Text]
  5. Vinceti M., Nacci G., Rocchi E., Cassinadri T., Vivoli R., Marchesi C., Bergomi M. Mortality in a population with long-term exposure to inorganic selenium via drinking water. J. Clin. Epidemiol., 53: 1062-1068, 2000.[Medline]
  6. Zheng W., Blot W. J., Diamond E. L., Norkus E. P., Spate V., Morris J. S., Comstock G. W. Serum micronutrients and the subsequent risk of oral and pharyngeal cancer. Cancer Res., 53: 795-798, 1993.[Abstract/Free Full Text]
  7. Nelson M. A., Reid M., Duffield-Lillico A. J., Marshall J. R. Prostate cancer and selenium. Urol. Clin. North Am., 29: 67-70, 2002.[Medline]
  8. Patterson B. H., Levander O. A. Naturally occurring selenium compounds in cancer chemoprevention trials: a workshop summary. Cancer Epidemiol. Biomark. Prev., 6: 63-69, 1997.[Abstract/Free Full Text]
  9. Kristal A. R., Moe G. False presumptions and continued surprises: how much do we really know about nutritional supplements and cancer risk?. Cancer Epidemiol. Biomark. Prev., 7: 849-850, 1998.[Medline]
  10. Vinceti M., Wei E. T., Malagoli C., Bergomi M., Vivoli G. Adverse health effects of selenium in humans. Rev. Environ. Health, 16: 233-251, 2001.[Medline]



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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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