Division of Hematology-Oncology, Massachusetts General Hospital Cancer Center, Boston, Massachusetts 02114, USA.
J Urol. 2011 Aug;186(2):482-6. doi: 10.1016/j.juro.2011.03.111. Epub 2011 Jun 15.
Androgen deprivation therapy for prostate cancer causes accelerated loss of bone mineral density and is associated with increased fracture risk. We evaluated risk factors associated with vertebral fractures among men enrolled in a fracture prevention trial.
Analysis included men receiving androgen deprivation therapy for prostate cancer and enrolled in a phase III fracture prevention trial. All men were 70 years old or older or had a low bone mineral density (T-score less than -1.5 for the lumbar spine or total hip). We analyzed demographic and laboratory characteristics of men with and those without vertebral fractures at study entry.
Of the 1,244 subjects 162 (13.0%) had a vertebral fracture at baseline. The 2 factors significantly associated with vertebral fractures were white race (p=0.028 compared with nonwhite race) and osteoporosis (p=0.002 for osteoporosis at any site, p=0.053 for osteoporosis at the spine, p=0.002 for osteoporosis at the hip). Lower bone mineral density was also significantly associated with vertebral fractures when analyzed as a continuous variable. Factors not associated with vertebral fractures included age, country of residence, androgen deprivation therapy duration at baseline, androgen deprivation therapy mode, body mass index, testosterone, estradiol, C-telopeptide, bone specific alkaline phosphatase and osteocalcin. Results were similar in analyses limited to men 70 years old or older.
White race and low bone mineral density were significantly associated with vertebral fractures in this study of men treated with androgen deprivation for prostate cancer. These observations should inform the assessment and management of fracture risk among such men.
前列腺癌的雄激素剥夺疗法会导致骨密度迅速下降,并增加骨折风险。我们评估了一项骨折预防试验中接受雄激素剥夺疗法的男性发生椎体骨折的相关风险因素。
分析纳入了接受雄激素剥夺疗法治疗前列腺癌并参加了一项 III 期骨折预防试验的男性。所有男性均为 70 岁或以上,或存在低骨密度(腰椎或全髋 T 评分<-1.5)。我们分析了研究入组时发生椎体骨折与未发生椎体骨折的男性的人口统计学和实验室特征。
在 1244 名受试者中,有 162 名(13.0%)在基线时发生了椎体骨折。与椎体骨折显著相关的 2 个因素是白种人(p=0.028 与非白种人相比)和骨质疏松症(任何部位骨质疏松症 p=0.002,脊柱骨质疏松症 p=0.053,髋关节骨质疏松症 p=0.002)。当作为连续变量进行分析时,较低的骨密度也与椎体骨折显著相关。与椎体骨折无关的因素包括年龄、居住国家、基线时的雄激素剥夺疗法持续时间、雄激素剥夺疗法模式、体重指数、睾酮、雌二醇、C 端肽、骨碱性磷酸酶和骨钙素。仅纳入 70 岁或以上男性的分析结果相似。
在这项接受雄激素剥夺疗法治疗前列腺癌的男性研究中,白种人和低骨密度与椎体骨折显著相关。这些观察结果应该为这些男性的骨折风险评估和管理提供信息。