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Prophylactic sildenafil citrate improves select aspects of sexual function in men treated with radiotherapy for prostate cancer.
Zelefsky, Michael J; Shasha, Daniel; Branco, Rebekah Dunn; Kollmeier, Marisa; Baser, Raymond E; Pei, Xin; Ennis, Ronald; Stock, Richard; Bar-Chama, Natan; Mulhall, John P.
Afiliação
  • Zelefsky MJ; Departments of Radiation Oncology and Urology, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: zelefskm@mskcc.org.
  • Shasha D; Department of Radiation Oncology, Continuum Cancer Center of New York, New York, New York.
  • Branco RD; Departments of Radiation Oncology and Urology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Kollmeier M; Departments of Radiation Oncology and Urology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Baser RE; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Pei X; Departments of Radiation Oncology and Urology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Ennis R; Department of Radiation Oncology, Continuum Cancer Center of New York, New York, New York.
  • Stock R; Departments of Radiation Oncology and Urology, Mt. Sinai Medical Center, New York, New York.
  • Bar-Chama N; Departments of Radiation Oncology and Urology, Mt. Sinai Medical Center, New York, New York.
  • Mulhall JP; Departments of Radiation Oncology and Urology, Memorial Sloan Kettering Cancer Center, New York, New York.
J Urol ; 192(3): 868-74, 2014 Sep.
Article em En | MEDLINE | ID: mdl-24603102
ABSTRACT

PURPOSE:

We studied adjuvant daily sildenafil citrate during and after radiotherapy for prostate cancer for erectile function preservation. MATERIALS AND

METHODS:

We performed a randomized, prospective trial of 279 patients with localized prostate cancer treated with radiotherapy who received sildenafil citrate (50 mg daily) or placebo (21 randomization). Medication/placebo was initiated 3 days before treatment and continued daily for 6 months. Before therapy and 3, 6, 9, 12, 18 and 24 months after radiotherapy patients completed the IIEF questionnaire, including the erectile function domain, the I-PSS questionnaire and the RAND SF-36®. All IIEF domains were scored.

RESULTS:

At 12 months erectile function scores were better for sildenafil citrate than placebo (p = 0.018), 73% of patients on sildenafil citrate vs 50% on placebo had mild/no erectile dysfunction (p = 0.024) and the sildenafil citrate arm had superior overall satisfaction (p = 0.027) and IIEF total scores (p = 0.043). At 24 months erectile function and IIEF scores were no longer significantly better for sildenafil citrate (p = 0.172 and 0.09, respectively) and yet overall satisfaction scores were higher (p = 0.033). Sexual desire scores in patients who received sildenafil citrate were higher at 24 months although they had completed drug therapy 18 months previously (p = 0.049). At 24 months 81.6% of patients on sildenafil citrate and 56.0% of those on placebo achieved functional erection with or without erectile dysfunction medication (p = 0.045).

CONCLUSIONS:

Daily sildenafil citrate during and after radiotherapy for prostate cancer was associated with improved overall sexual function compared with placebo for various sexual function domains. To our knowledge this is the largest randomized, prospective, controlled trial to show the usefulness of a phosphodiesterase-5 inhibitor as a rehabilitation strategy in patients with prostate cancer who received radiation therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piperazinas / Neoplasias da Próstata / Sulfonas / Inibidores da Fosfodiesterase 5 / Disfunção Erétil Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piperazinas / Neoplasias da Próstata / Sulfonas / Inibidores da Fosfodiesterase 5 / Disfunção Erétil Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article