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首页> 外文期刊>BJU international >Impact of androgen suppression and zoledronic acid on bone mineral density and fractures in the Trans-Tasman Radiation Oncology Group (TROG) 03.04 Randomised Androgen Deprivation and Radiotherapy (RADAR) randomized controlled trial for locally advanced prostate cancer
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Impact of androgen suppression and zoledronic acid on bone mineral density and fractures in the Trans-Tasman Radiation Oncology Group (TROG) 03.04 Randomised Androgen Deprivation and Radiotherapy (RADAR) randomized controlled trial for locally advanced prostate cancer

机译:跨塔斯曼放射肿瘤学组(TROG)雄激素抑制和唑来膦酸对骨矿物质密度和骨折的影响03.04局部晚期前列腺癌的随机性雄激素剥夺和放射治疗(RADAR)随机对照试验

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摘要

Objective To study the influence of adjuvant androgen suppression and bisphosphonates on incident vertebral and non-spinal fracture rates and bone mineral density (BMD) in men with locally advanced prostate cancer. Patients and Methods Between 2003 and 2007, 1071 men with locally advanced prostate cancer were randomly allocated, using a 2 × 2 trial design, to 6 months i.m. leuprorelin (androgen suppression [AS]) before radiotherapy alone ± 12 months additional leuprorelin ± 18 months zoledronic acid (ZdA), commencing at randomization. The main endpoint was incident thoraco-lumbar vertebral fractures, which were assessed radiographically at randomization and at 3 years, then reassessed by centralized review. Subsidiary endpoints included incident non-spinal fractures, which were documented throughout follow-up, and BMD, which was measured in 222 subjects at baseline, 2 years and 4 years. Results Incident vertebral fractures at 3 years were observed in 132 subjects. Their occurrence was not increased by 18 months' AS, nor reduced by ZdA. Incident non-spinal fractures occurred in 72 subjects and were significantly related to AS duration but not to ZdA. Osteopenia and osteoporosis prevalence rates at baseline were 23.4 and 1.4%, respectively, at the hip. Treatment for 6 and 18 months with AS caused significant reductions in hip BMD at 2 and 4 years (P < 0.01) and ZdA prevented these losses at both time points. Conclusion In an AS-na?ve population, 18 months of ZdA treatment prevented the sustained BMD losses caused by 18 months of AS treatment; however, the study power was insufficient to show that AS duration or ZdA influenced vertebral fracture rates.
机译:目的研究佐剂抑制雄激素和双膦酸盐对局部晚期前列腺癌男性患者的椎骨和非脊髓骨折发生率以及骨矿物质密度(BMD)的影响。患者和方法2003年至2007年之间,采用2×2试验设计,将1071名患有局部晚期前列腺癌的男性随机分配至6个月。单独接受放疗前的亮丙瑞林(雄激素抑制[AS])±12个月后再加亮白瑞林±18个月唑来膦酸(ZdA),随机开始。主要终点是发生的胸腰椎脊椎骨折,在随机和3年时进行了影像学评估,然后通过集中检查进行了重新评估。辅助终点包括在整个随访过程中记录的非脊柱骨折事件,以及在基线,2年和4年时对222名受试者进行测量的BMD。结果132例患者在3年时发生了脊椎骨折。 AS出现18个月后,它们的发生没有增加,ZdA也没有减少它们的发生。非脊柱骨折发生在72名受试者中,与AS持续时间显着相关,但与ZdA无关。髋部骨质减少症和骨质疏松症患病率在基线分别为23.4%和1.4%。用AS治疗6个月和18个月可导致2年和4年髋关节BMD显着降低(P <0.01),ZdA可以在两个时间点均防止这些损失。结论:对于单纯性天真的人群,ZdA治疗18个月可预防18个月AS治疗引起的持续BMD损失。但是,研究能力不足以表明AS持续时间或ZdA影响椎骨骨折率。

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