Diamond Terrence H, Higano Celestia S, Smith Matthew R, Guise Theresa A, Singer Frederick R
Department of Medicine, University of New South Wales, St. George Hospital Campus, Sydney, Australia.
Cancer. 2004 Mar 1;100(5):892-9. doi: 10.1002/cncr.20056.
Androgen-deprivation therapy (ADT) is prescribed with increasing frequency for men with prostate carcinoma. There is growing concern about the effects of such therapy on the skeleton. In the current review, the authors addressed the current research, diagnostic methods, and treatment recommendations for bone loss and osteoporosis in men with prostate carcinoma who received ADT.
Data were obtained from electronic literature searches (for the years 1986 through 2002) and from abstracts and meeting proceedings. All randomized and nonrandomized clinical trials, retrospective studies, and cross-sectional studies of osteoporosis in men with prostate carcinoma who received ADT with or without other therapies were reviewed.
The findings confirmed that ADT resulted in significant bone loss in men with prostate carcinoma. Bone mineral density (BMD) of the hip, as measured by dual-energy X-ray absorptiometry (DXA), is considered the preferred site of assessment in older men. Spinal BMD is equally important, although careful interpretation of spinal DXA values is required, because of coexisting facet joint disease and extravertebral calcification. Osteoporosis is diagnosed when BMD is > 2.5 standard deviations below a reference mean. Men with prostate carcinoma who were treated with ADT had average BMD measurements below those of eugonadal men. Rates of bone loss ranged from 2% to 8% in the lumbar spine and from 1.8% to 6.5% in the femoral neck during the initial 12 months of continuous ADT. Retrospective data indicated an increased risk of fracture in men with prostate carcinoma who were treated with ADT.
For men with prostate carcinoma who are at high risk for osteoporosis and fractures, clinical management should be dictated by the results of radiographic and DXA skeletal assessment.
雄激素剥夺疗法(ADT)在前列腺癌男性患者中的应用频率日益增加。人们越来越关注这种疗法对骨骼的影响。在当前的综述中,作者阐述了针对接受ADT的前列腺癌男性患者骨丢失和骨质疏松的当前研究、诊断方法及治疗建议。
数据来自电子文献检索(1986年至2002年)以及摘要和会议记录。对所有接受或未接受其他疗法的ADT前列腺癌男性患者骨质疏松的随机和非随机临床试验、回顾性研究及横断面研究进行了综述。
研究结果证实,ADT导致前列腺癌男性患者出现显著骨丢失。采用双能X线吸收法(DXA)测量的髋部骨密度(BMD)被认为是老年男性评估的首选部位。脊柱BMD同样重要,不过由于存在小关节疾病和椎体外钙化,需要仔细解读脊柱DXA值。当BMD低于参考均值2.5个标准差时可诊断为骨质疏松。接受ADT治疗的前列腺癌男性患者的平均BMD测量值低于性腺功能正常的男性。在持续ADT的最初12个月中,腰椎的骨丢失率为2%至8%,股骨颈的骨丢失率为1.8%至6.5%。回顾性数据表明,接受ADT治疗的前列腺癌男性患者骨折风险增加。
对于骨质疏松和骨折高危的前列腺癌男性患者,临床管理应依据影像学和DXA骨骼评估结果来决定。