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Cancer Prevention |
1 Divisions of Chemoprevention, 2 Laboratory Medicine, 3 Cancer Epidemiology Center, Cancer Council of Victoria, Melbourne, Australia; and 4 Clinical Pathology, National Institute for Cancer Research; and 5 Division of Medical and Preventive Oncology, Galliera Hospital, Genoa, Italy
Requests for reprints: Andrea Decensi, Division of Chemoprevention, European Institute of Oncology, via Ripamonti, 435, 20141 Milan, Italy. Phone: 39-2-57489861; Fax: 39-2-57489809; E-mail: andrea.decensi{at}ieo.it.
Purpose: Fenretinide (4-HPR) is a synthetic retinoid that has shown a preventive activity in prostate cancer animal models.
Experimental Design: We measured the changes in total and free prostate-specific antigen (PSA) and its association with insulin-like growth factor I (IGF-I) and IGFBP-3 levels after 1 year of treatment in 24 subjects given 4-HPR and 24 control subjects enrolled in a randomized bladder cancer prevention trial.
Results: No significant effect of 4-HPR was observed on total and free fraction of PSA levels. The median percentage [95 confidence interval (95% CI)] change for % free PSA and total PSA in the 4-HPR and the control group were, respectively, 7.6 (95% CI, 4.0 to 69.3) versus 5.1 (95% CI, 21.4 to 59.8) and 7.8 (95% CI, 18.2 to 52.5) versus 12.3 (95% CI, 44.6 to 9.6). However, in patients ages <60 years, there was a trend to an increase of total free PSA and % free PSA after treatment with 4-HPR that was different from a trend to a decrease in the control group (P = 0.002 and 0.052, respectively). The interaction between age and treatment was statistically significant on free PSA (P = 0.001). A similar pattern was noted with smoking status (P = 0.011 for the interaction on free PSA). No association was observed between PSA levels and IGF-I or IGFBP-3 levels.
Conclusions: We conclude that 4-HPR has no significant effect on circulating PSA, but it increases significantly free PSA levels in subjects younger than 60 years and in nonsmokers. These effects might support an activity in prostate cancer prevention but further studies are required.
Key Words: Retinoids chemoprevention biomarkers prostate neoplasms
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