Literature DB >> 9426725

Tamoxifen for flutamide/finasteride-induced gynecomastia.

V R Staiman1, F C Lowe.   

Abstract

OBJECTIVES: Current therapies for advanced prostate carcinoma lead to a marked decrease in serum testosterone levels, which renders patients impotent. In preliminary studies, combination therapy with flutamide and finasteride has been used as an alternative therapy for the treatment of prostate carcinoma because potency can be preserved. Both of these agents can cause gynecomastia and breast/nipple tenderness.
METHODS: Six men being treated for advanced prostate carcinoma with flutamide/finasteride combination therapy developed painful gynecomastia, which was treated with tamoxifen 10 to 30 mg/day for 1 month. Clinical follow-up included breast measurements and determination of prostate-specific antigen (PSA), testosterone, and estradiol levels.
RESULTS: While on this combination therapy for prostate carcinoma, 4 of 6 patients experienced a decrease in PSA level to less than 0.5 ng/mL. All patients remained potent. Serum testosterone increased in each patient who had a baseline level drawn. Estradiol levels were noted to be elevated in 4 of 6 patients at the time of evaluation for gynecomastia. After treatment with tamoxifen, circulating estradiol levels increased in 3 patients from 1.3 to 2.2 times the baseline level. Five patients experienced complete resolution of breast and nipple pain on tamoxifen 10 mg/day within the first month. The other patient had to be treated with 30 mg/day for 1 additional month, which subsequently resulted in pain resolution.
CONCLUSIONS: These preliminary results suggest that low-dose tamoxifen is useful in treating painful gynecomastia for those patients on flutamide/finasteride combination therapy for advanced prostate carcinoma.

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Year:  1997        PMID: 9426725     DOI: 10.1016/S0090-4295(97)00457-3

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  7 in total

1.  Management options for gynaecomastia and breast pain associated with nonsteroidal antiandrogen therapy : case report series.

Authors:  I Leibovitch; D Gillatt; P Hopwood; P Iversen; R E Mansel; D McLeod; R Vela-Navarrete; P Richaud; W See; C Tyrrell; M Wirth
Journal:  Clin Drug Investig       Date:  2003       Impact factor: 2.859

Review 2.  Complications of androgen deprivation therapy in men with prostate cancer.

Authors:  Allen C Chen; Daniel P Petrylak
Journal:  Curr Oncol Rep       Date:  2004-05       Impact factor: 5.075

3.  Multiple structural and functional abnormalities in the p450 aromatase expressing transgenic male mice are ameliorated by a p450 aromatase inhibitor.

Authors:  Xiangdong Li; Leena Strauss; Sari Mäkelä; Tomi Streng; Ilpo Huhtaniemi; Risto Santti; Matti Poutanen
Journal:  Am J Pathol       Date:  2004-03       Impact factor: 4.307

Review 4.  Complications of androgen-deprivation therapy in men with prostate cancer.

Authors:  Allen C Chen; Daniel P Petrylak
Journal:  Curr Urol Rep       Date:  2005-05       Impact factor: 2.862

5.  Influence of Postoperative Finasteride Therapy on Recurrence of Gynecomastia After Mastectomy in Men Taking Finasteride for Alopecia.

Authors:  Seung Geun Lee; Pyoung Jae Park; Sung Ryul Lee; Bum Hwan Koo; Geon Young Byun; Myoung Jin Kim; Hyok Jo Kang; Sarang Kim; Beom Seok Oh; Young Hyun Lee
Journal:  Am J Mens Health       Date:  2019 Sep-Oct

Review 6.  Tamoxifen for the management of breast events induced by non-steroidal antiandrogens in patients with prostate cancer: a systematic review.

Authors:  Frank Kunath; Bastian Keck; Gerd Antes; Bernd Wullich; Joerg J Meerpohl
Journal:  BMC Med       Date:  2012-08-28       Impact factor: 8.775

7.  An open label, dose response study to determine the effect of a dietary supplement on dihydrotestosterone, testosterone and estradiol levels in healthy males.

Authors:  Fru Angwafor; Mark L Anderson
Journal:  J Int Soc Sports Nutr       Date:  2008-08-12       Impact factor: 5.150

  7 in total

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