Longitudinal analysis of sexual function reported by men in the prostate cancer prevention trial

被引:58
作者
Moinpour, Carol M.
Darke, Amy K.
Donaldson, Gary W.
Thompson, Ian M., Jr.
Langley, Connie
Ankerst, Donna Pauler
Patrick, Donald L.
Ware, John E.
Ganz, Patricia A.
Shumaker, Sally A.
Lippman, Scott M.
Coltman, Charles A., Jr.
机构
[1] Fred Hutchinson Canc Res Ctr, Operat Off, SW Oncol Grp, Stat Ctr, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[3] Univ Utah, Dept Anesthesiol, Salt Lake City, UT 84112 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Urol, San Antonio, TX 78229 USA
[5] Wilford Hall USAF Med Ctr, Dept Urol, Lackland AFB, TX USA
[6] Univ Munich, Inst Med Informat Biometry & Epidemiol, D-80539 Munich, Germany
[7] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA
[8] QualityMetr Inco, Lincoln, RI USA
[9] Hlth Assessment Lab, Waltham, MA USA
[10] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90024 USA
[11] Univ Calif Los Angeles, Sch Publ Hlth, Los Angeles, CA 90024 USA
[12] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
[13] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27109 USA
[14] Univ Texas, MD Anderson Canc Ctr, Dept Clin Canc Prevent, Houston, TX 77030 USA
[15] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[16] SW Oncol Grp, Canc Control & Prevent, Operat Off, San Antonio, TX USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2007年 / 99卷 / 13期
关键词
D O I
10.1093/jnci/djm023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The Prostate Cancer Prevention Trial (PCPT) was a randomized, double-blind, placebo-controlled study of the efficacy of finasteride in preventing prostate cancer in 18882 men aged 55 years or older. The PCPT offered an opportunity to prospectively study the effects of finasteride and other covariates on sexual dysfunction. Methods We assessed sexual dysfunction in 17313 PCPT participants during a 7-year period. A battery of questionnaires assessed sexual dysfunction (Sexual Activity Scale score); age; race; SF-36 Mental Health Inventory-5, Physical Function, and Vitality scores; body mass index; smoking status; and the presence of diabetes and hypertension. Assessments began at month 6 after random assignment and included the Sexual Activity Scale score at randomization as a covariate. Two-sided general t tests, with a cutoff of P value less than .05, were used to determine the statistical significance for mixed model effects with correlated random time slopes and intercepts. The changing impact of covariates on sexual dysfunction was also assessed at 6 months, 3.5 years, and 6.5 years after randomization. Results Finasteride increased sexual dysfunction only slightly and its impact diminished over time; the increase in the Sexual Activity Scale score relative to placebo of 3.21 points (95% confidence interval [Cl] = 2.83 to 3.59 points; P <.001) at the first assessment decreased to 2.11 points (95% Cl = 1.44 to 2.81 points; P <.001) at the end of study. These Sexual Activity score values were small on a scale of 0-100, the range observed in the study, and in comparison with individual variation. After adjustment for all covariates, mean sexual dysfunction increased in both arms from baseline (6 months after randomization) by 1.26 Sexual Activity points (95% Cl 1.16 to 1.36 points; P <.001) per year, corresponding to a cumulative increase of 8.22 points (95% Cl 7.52 to 8.92 points; P <.001) over the study period. Conclusions The effect of finasteride on sexual functioning is minimal for most men and should not impact the decision to prescribe or take finasteride.
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收藏
页码:1025 / 1035
页数:11
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