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July 1, 1998Journal of Clinical Oncology255 citations

Pilot evaluation of venlafaxine hydrochloride for the therapy of hot flashes in cancer survivors.

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CLCharles L. LoprinziTPThomas M. PisanskyRFRafaël Fonseca

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Abstract

PURPOSE: Hot flashes can be a prominent clinical problem for breast cancer survivors and men who undergo androgen-deprivation therapy. Anecdotal information suggested a low dose of a relatively new antidepressant, venlafaxine, could abrogate this clinical problem. MATERIALS AND METHODS: This study included 28 consecutive assessable patients entered onto a phase II clinical trial. Hot flash data were collected by daily diary questionnaires during a 1-week baseline period and then for 4 weeks, during which time patients received venlafaxine 12.5 mg orally twice daily. RESULTS: Fifty-eight percent of patients who completed the study had a greater than 50% reduction in hot flash scores (frequency times severity) during the fourth treatment week as compared with the baseline week. Median weekly hot flash scores were reduced by 55% from baseline during the fourth week of venlafaxine therapy. Therapy was generally well tolerated and appeared to alleviate fatigue, sweating, and trouble sleeping. CONCLUSION: Venlafoxine appears to represent an efficacious new method to alleviate hot flashes. Further evaluation of this compound for alleviating hot flashes is indicated.

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Cite This Study

Loprinzi et al. (1998) studied this question.

synapsesocial.com/papers/6a204a10e9ca693ff1e715ddhttps://doi.org/10.1200/jco.1998.16.7.2377
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