Regional Cancer Centre, Karolinska University Hospital, Stockholm, Sweden.
Eur J Cancer. 2012 Jul;48(11):1672-81. doi: 10.1016/j.ejca.2012.01.035. Epub 2012 Mar 3.
Prostate cancer patients have an increased risk of fractures as a consequence of skeletal metastases and osteoporosis induced by endocrine treatment. Data on incidence of fractures and risks in subgroups of men with prostate cancer are sparse. Our aim with this study is to report the risk of fractures among men with prostate cancer in a nationwide population-based study.
We identified 76,600 Swedish men diagnosed with prostate cancer 1997-2006 in the Prostate Cancer Data Base (PCBaSe) Sweden and compared the occurrence of fractures requiring hospitalisation with the Swedish male population.
Only men treated with gonadotropin releasing-hormone (GnRH) agonists or orchiectomy had increased incidence and increased relative risk of fractures requiring hospitalisation. Men treated with GnRH agonists had 9.8 and 6.3/1000 person-years higher incidence of any fracture and hip fracture requiring hospitalisation than the general population. The corresponding increases in incidence for men treated with orchiectomy were 16 and 12/1000 person-years, respectively. Men treated with orchiectomy, GnRH agonists, and antiandrogen monotherapy, had SIR for hip fracture of 2.0 (95% Confidence Interval 1.8-2.2), 1.6 (95% CI 1.5-1.8) and 0.9 (95% CI 0.7-1.1), respectively. Men treated with a curative intent (radical prostatectomy or radiotherapy) or managed with surveillance had no increased risk of fractures. Older men had the highest incidence of fractures while younger men had the highest relative risk.
Prostate cancer patients treated with GnRH agonists or orchiectomy have significantly increased risk of fractures requiring hospitalisation while patients treated with antiandrogen monotherapy had no increase in such fractures. In absolute terms the excess risk in men treated with GnRH agonists corresponded to almost 10 extra fractures leading to hospitalisation per 1000 patient-years. Effects on bone density should be considered for men on long-term endocrine treatment. Unwarranted use of orchiectomy and GnRH agonists should be avoided.
前列腺癌患者由于骨骼转移和内分泌治疗引起的骨质疏松症,骨折风险增加。关于前列腺癌患者骨折的发病率和风险亚组的数据很少。我们的研究目的是在一项全国范围内基于人群的研究中报告前列腺癌男性的骨折风险。
我们在瑞典前列腺癌数据库(PCBaSe Sweden)中确定了 1997-2006 年间诊断为前列腺癌的 76600 名瑞典男性,并将骨折的发生情况与瑞典男性人群进行了比较。
只有接受促性腺激素释放激素(GnRH)激动剂或睾丸切除术治疗的男性骨折发生率增加,且骨折住院的相对风险增加。接受 GnRH 激动剂治疗的男性,任何骨折和髋部骨折的发生率分别比普通人群高 9.8 和 6.3/1000 人年。睾丸切除术治疗的男性相应的发病率增加分别为 16 和 12/1000 人年。接受睾丸切除术、GnRH 激动剂和抗雄激素单药治疗的男性,髋部骨折的 SIR 分别为 2.0(95%置信区间 1.8-2.2)、1.6(95%置信区间 1.5-1.8)和 0.9(95%置信区间 0.7-1.1)。接受根治性前列腺切除术或放疗治疗或接受监测治疗的男性骨折风险没有增加。年龄较大的男性骨折发生率最高,而年龄较小的男性相对风险最高。
接受 GnRH 激动剂或睾丸切除术治疗的前列腺癌患者骨折住院的风险显著增加,而接受抗雄激素单药治疗的患者骨折风险没有增加。从绝对风险来看,接受 GnRH 激动剂治疗的男性每年每 1000 名患者中增加近 10 例骨折导致住院治疗。应考虑长期内分泌治疗对骨密度的影响。应避免不必要的睾丸切除术和 GnRH 激动剂的使用。