| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Division of Chemoprevention [A. G-G., H. J., B. B., S. D., A. D.], Division of Epidemiology and Biostatistics [L. B., C. R.], Laboratory Medicine Unit [M-T. S.], European Institute of Oncology, 20141 Milan, Italy; the League Against Cancer, Milan, Italy [L. C., C. L.]; and Haukeland Hospital, N-5021 Bergen, Norway [E. A. L.]
We have shown previously that a reduction from the conventional dose of tamoxifen is associated with a comparable modulation of circulating biomarkers, including insulin-like growth factor-I and cholesterol. In the present study, we have correlated serum tamoxifen elimination with biomarker recovery in healthy subjects completing a 5-year intervention period. Tamoxifen, N-desmethyltamoxifen, and biomarker levels were measured at 0 (baseline), 2, 4, and 6 weeks after completion of treatment in 23 healthy postmenopausal women allocated to tamoxifen 20 mg/day and in 6 women allocated to placebo. Mean (±SD) serum tamoxifen and N-desmethyltamoxifen concentrations were, respectively, 141 ± 50 and 226 ± 77 ng/ml at baseline, 36 ± 19 and 99 ± 46 at 2 weeks, 20 ± 15 and 61 ± 37 at 4 weeks, and 12 ± 9 and 36 ± 26 at 6 weeks. Serum tamoxifen and N-desmethyltamoxifen half-lives were 9 and 13 days, respectively. Body mass index was associated positively with drugs serum half-life. Compared with baseline values, the percentage increase in total cholesterol, low-density lipoprotein cholesterol, and insulin-like growth factor-I 4 weeks after treatment completion was 5, 9, and 14%, respectively. No change during the 6-week period was observed in the placebo arm. Our findings indicate that the biomarker recovery is slower than serum tamoxifen elimination, suggesting that low tamoxifen concentrations may still exert a biological effect. In addition, the prolonged half-life of tamoxifen and metabolite provides the rationale for a weekly administration of the drug in a preventive context. However, the clinical implications of our findings remain to be defined.
This article has been cited by other articles:
![]() |
A. Decensi, S. Gandini, D. Serrano, M. Cazzaniga, M. Pizzamiglio, F. Maffini, G. Pelosi, C. Daldoss, U. Omodei, H. Johansson, et al. Randomized Dose-Ranging Trial of Tamoxifen at Low Doses in Hormone Replacement Therapy Users J. Clin. Oncol., September 20, 2007; 25(27): 4201 - 4209. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. H. Wu, M. C. Pike, L. D. Williams, D. Spicer, C.-C. Tseng, M. I. Churchwell, and D. R. Doerge Tamoxifen, Soy, and Lifestyle Factors in Asian American Women With Breast Cancer J. Clin. Oncol., July 20, 2007; 25(21): 3024 - 3030. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. Veronesi, P. Maisonneuve, and A. Decensi Tamoxifen: An Enduring Star J Natl Cancer Inst, February 21, 2007; 99(4): 258 - 260. [Full Text] [PDF] |
||||
![]() |
A. Decensi, C. Robertson, G. Viale, F. Pigatto, H. Johansson, E. R. Kisanga, P. Veronesi, R. Torrisi, M. Cazzaniga, S. Mora, et al. A Randomized Trial of Low-Dose Tamoxifen on Breast Cancer Proliferation and Blood Estrogenic Biomarkers J Natl Cancer Inst, June 4, 2003; 95(11): 779 - 790. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |