Oh Daniel S, Koontz Bridget, Freedland Stephen J, Gerber Leah, Patel Pretesh, Lewis Stephen, Yoo David S, Oleson James, Salama Joseph K
Durham VA Medical Center, Duke University, Durham, NC, USA.
World J Urol. 2015 Jan;33(1):93-7. doi: 10.1007/s00345-014-1281-x. Epub 2014 Mar 27.
PURPOSE/OBJECTIVE(S): Recent in vitro and in vivo evidence has suggested that statin medications may have anticancer activity. We sought to determine whether statin use was associated with improved clinical outcome in men treated with brachytherapy for prostate cancer.
MATERIALS/METHODS: A database of men with prostate cancer treated with permanent Iodine-125 brachytherapy between January 1999 and February 2009 was retrospectively analyzed. Standard guidelines (i.e., American Brachytherapy Society selection criteria) were used for selecting patients for brachytherapy. Biochemical failure was defined using the Phoenix definition.
From a total of 247 men with prostate adenocarcinoma treated with brachytherapy, 174 patients (70 %) were identified as using statin medications, either during initial visit or during follow-up. Median PSA follow-up was 51 months after date of implant (range 9.4-140.35). Overall biochemical failure rate was 7.3 % (18 patients). On univariate analysis, statin use was associated with significantly improved freedom from biochemical failure [hazard ratio (HR) 0.28; 95 % CI 0.10-0.72; p < 0.01 by log-rank test]. In multivariate Cox analysis performed with the variables statin use, pretreatment PSA, clinical T stage, Gleason score, and D90 or V100, statin use remained significantly associated with improved freedom from biochemical failure (HR 0.288; 95 % CI 0.086-0.886; p = 0.0299).
Statin use was associated with a significant improvement in freedom from biochemical failure in this cohort of men treated with brachytherapy for prostate cancer. Further investigation into the favorable effect of statin use on brachytherapy and radiation therapy in general is warranted, including prospective trials.
近期的体外和体内证据表明,他汀类药物可能具有抗癌活性。我们试图确定在接受前列腺癌近距离放射治疗的男性中,使用他汀类药物是否与改善临床结局相关。
回顾性分析了1999年1月至2009年2月期间接受永久性碘-125近距离放射治疗的前列腺癌男性患者数据库。采用标准指南(即美国近距离放射治疗学会选择标准)选择接受近距离放射治疗的患者。生化失败采用Phoenix定义。
在总共247例接受近距离放射治疗的前列腺腺癌男性患者中,174例(70%)在初次就诊或随访期间被确定使用他汀类药物。植入后前列腺特异性抗原(PSA)的中位随访时间为51个月(范围9.4 - 140.35个月)。总体生化失败率为7.3%(18例患者)。单因素分析显示,使用他汀类药物与生化失败-free显著改善相关[风险比(HR)0.28;95%置信区间0.10 - 0.72;对数秩检验p < 0.01]。在对他汀类药物使用、治疗前PSA、临床T分期、Gleason评分和D90或V100等变量进行的多因素Cox分析中,他汀类药物使用仍与生化失败-free的改善显著相关(HR 0.288;95%置信区间0.086 - 0.886;p = 0.0299)。
在这组接受前列腺癌近距离放射治疗的男性中,使用他汀类药物与生化失败-free的显著改善相关。有必要对他汀类药物使用对近距离放射治疗及一般放射治疗的有利影响进行进一步研究,包括前瞻性试验。