Public Health Sciences Division, Fred Hutchinson Cancer Research Center, M3-C102 1100 Fairview Ave North, PO Box 19024 Seattle, WA 98109-1024, USA.
J Natl Cancer Inst. 2012 Sep 19;104(18):1373-85. doi: 10.1093/jnci/djs359. Epub 2012 Sep 12.
The Prostate Cancer Prevention Trial (PCPT)-a randomized placebo-controlled study of the efficacy of finasteride in preventing prostate cancer-offered the opportunity to prospectively study effects of finasteride and other covariates on the health-related quality of life of participants in a multiyear trial.
We assessed three health-related quality-of-life domains (measured with the Health Survey Short Form-36: Physical Functioning, Mental Health, and Vitality scales) via questionnaires completed by PCPT participants at enrollment (3 months before randomization), at 6 months after randomization, and annually for 7 years. Covariate data obtained at enrollment from patient-completed questionnaires were included in our model. Mixed-effects model analyses and a cross-sectional presentation at three time points began at 6 months after randomization. All statistical tests were two-sided.
For the physical function outcome (n = 16 077), neither the finasteride main effect nor the finasteride interaction with time were statistically significant. The effects of finasteride on physical function were minor and accounted for less than a 1-point difference over time in Physical Functioning scores (mixed-effect estimate = 0.07, 95% confidence interval [CI] = -0.28 to 0.42, P = .71). Comorbidities such as congestive heart failure (estimate = -5.64, 95% CI = -7.96 to -3.32, P < .001), leg pain (estimate = -2.57, 95% CI = -3.04 to -2.10, P < .001), and diabetes (estimate = -1.31, 95% CI = -2.04 to -0.57, P < .001) had statistically significant negative effects on physical function, as did current smoking (estimate = -2.34, 95% CI = -2.97 to -1.71, P < .001) and time on study (estimate = -1.20, 95% CI = -1.36 to -1.03, P < .001). Finasteride did not have a statistically significant effect on the other two dependent variables, mental health and vitality, either in the mixed-effects analyses or in the cross-sectional analysis at any of the three time points.
Finasteride did not negatively affect SF-36 Physical Functioning, Mental Health, or Vitality scores.
前列腺癌预防试验(PCPT)是一项关于非那雄胺预防前列腺癌的疗效的随机安慰剂对照研究,为前瞻性研究非那雄胺及其他协变量对多年度试验参与者健康相关生活质量的影响提供了机会。
我们通过问卷调查评估了三个健康相关的生活质量领域(使用健康调查短表-36:身体机能、心理健康和活力量表),PCPT 参与者在入组时(随机分组前 3 个月)、随机分组后 6 个月以及随后 7 年内每年完成一次。入组时从患者完成的问卷中获得的协变量数据被纳入我们的模型。混合效应模型分析和在三个时间点的横断面呈现从随机分组后 6 个月开始。所有统计检验均为双侧。
对于身体功能结果(n=16077),非那雄胺的主要作用或非那雄胺与时间的相互作用均无统计学意义。非那雄胺对身体功能的影响较小,在身体机能评分上的差异不到 1 分(混合效应估计值=0.07,95%置信区间[CI]为-0.28 至 0.42,P=0.71)。充血性心力衰竭(估计值=-5.64,95%CI=-7.96 至-3.32,P<.001)、腿部疼痛(估计值=-2.57,95%CI=-3.04 至-2.10,P<.001)和糖尿病(估计值=-1.31,95%CI=-2.04 至-0.57,P<.001)等合并症以及当前吸烟(估计值=-2.34,95%CI=-2.97 至-1.71,P<.001)和研究时间(估计值=-1.20,95%CI=-1.36 至-1.03,P<.001)对身体功能均有统计学上的负面影响。非那雄胺在混合效应分析或在三个时间点的任何一个时间点的横断面分析中,对其他两个依赖变量,即心理健康和活力,均无统计学意义上的影响。
非那雄胺未对 SF-36 身体机能、心理健康或活力评分产生负面影响。