Department of Urology, Tokyo Metropolitan Police Hospital, 4-22-1 Nakano, Nakano-ku, Tokyo, 164-8541, Japan.
Division of Endocrine and Breast Surgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.
J Bone Miner Metab. 2024 Mar;42(2):223-232. doi: 10.1007/s00774-024-01497-4. Epub 2024 Mar 17.
Androgen deprivation therapy (ADT) is widely used for the treatment of prostate cancer. ADT is associated with reduced bone density leading to an increased risk of osteoporotic fracture. The objective of this retrospective cohort study was to quantify fracture risk in men treated with ADT for prostate cancer in real-world practice in Japan.
Data were extracted from the Japanese Medical Data Vision (MDV) database. Men initiating ADT for treatment of prostate cancer between April 2010 and March 2021 were identified and matched to a cohort of prostate cancer patients not taking ADT using a propensity score. Fracture rates were estimated by a cumulative incidence function and compared between cohorts using a Cox cause-specific hazard model. Information was extracted on demographics, comorbidities and bone densitometry.
30,561 men with PC starting ADT were matched to 30,561 men with prostate cancer not treated with ADT. Following ADT initiation, <5% of men underwent bone densitometry. Prescription of ADT was associated with an increased fracture risk compared to not taking ADT (adjusted hazard ratio: 1.63 [95% CI 1.52-1.75]).
ADT is associated with a 1.6-fold increase in the risk of osteoporotic fracture in men with prostate cancer. Densitometry in this population is infrequent and monitoring urgently needs to be improved in order to implement effective fracture prevention.
雄激素剥夺疗法(ADT)广泛用于治疗前列腺癌。ADT 会导致骨密度降低,从而增加骨质疏松性骨折的风险。本回顾性队列研究的目的是在日本的真实环境中量化接受 ADT 治疗的前列腺癌男性的骨折风险。
从日本医疗数据视觉(MDV)数据库中提取数据。确定 2010 年 4 月至 2021 年 3 月期间因前列腺癌开始接受 ADT 治疗的男性,并使用倾向评分与未接受 ADT 的前列腺癌患者队列进行匹配。使用累积发生率函数估计骨折发生率,并使用 Cox 因果风险模型比较队列之间的发生率。提取人口统计学、合并症和骨密度测量的信息。
30561 名开始接受 ADT 的 PC 男性与 30561 名未接受 ADT 的前列腺癌男性相匹配。在开始 ADT 治疗后,<5%的男性接受了骨密度测量。与未接受 ADT 治疗相比,接受 ADT 治疗与骨折风险增加相关(调整后的危险比:1.63 [95%CI 1.52-1.75])。
ADT 与前列腺癌男性骨质疏松性骨折风险增加 1.6 倍相关。该人群中骨密度测量的频率较低,迫切需要改进监测,以实施有效的骨折预防。