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  • Randomized trial to assess the impact of venlafaxine and soy protein on hot flashes and quality of life in men with prostate cancer.

Randomized trial to assess the impact of venlafaxine and soy protein on hot flashes and quality of life in men with prostate cancer.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology (2013-10-02)
Mara Z Vitolins, Leah Griffin, W Vic Tomlinson, Jacqueline Vuky, Paul T Adams, Dawn Moose, Bart Frizzell, Glenn J Lesser, Michelle Naughton, James E Radford, Edward G Shaw
ABSTRACT

Hot flashes occur in approximately 80% of androgen-deprived men. Few intervention studies have been conducted to relieve hot flashes in men. Eligible androgen-deprived men were randomly assigned to one of four daily regimens (2 × 2 factorial design) for 12 weeks: milk protein powder and placebo pill, venlafaxine and milk protein powder, soy protein powder and placebo pill, or venlafaxine and soy protein powder. The primary end point was hot flash symptom severity score (HFSSS), defined as number of hot flashes times severity. The secondary end point was quality of life (QoL), assessed by using the Functional Assessment of Cancer Therapy-Prostate. In all, 120 men age 46 to 91 years participated. Most were white (78%) and overweight or obese (83%). Toxicity was minimal. Neither venlafaxine nor soy protein alone or in combination had a significant effect on HFSSS. Soy protein, but not venlafaxine, improved measures of QoL. In androgen-deprived men, neither venlafaxine nor soy proved effective in reducing hot flashes. Interventions that appear effective for decreasing hot flashes in women may not always turn out to be effective in men.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Venlafaxine hydrochloride, ≥98% (HPLC), powder
Supelco
Venlafaxine hydrochloride solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
Venlafaxine hydrochloride, European Pharmacopoeia (EP) Reference Standard
Venlafaxine for system suitability, European Pharmacopoeia (EP) Reference Standard