Department of Urology, Tokyo Metropolitan Police Hospital, 4-22-1, Nakano, Nakano-Ku, Tokyo, 164-8541, Japan.
J Bone Miner Metab. 2023 Nov;41(6):822-828. doi: 10.1007/s00774-023-01456-5. Epub 2023 Jul 27.
Androgen deprivation therapy (ADT) for prostate cancer causes cancer treatment-induced bone loss (CTIBL), increases the fracture risk 2-3 times, and worsens life prognoses. The Japan Society of Bone and Mineral Research (JSBMR) created a CTIBL treatment manual in 2020; however, no study has validated its use in patients with ADT/CTIBL prostate cancer.
This study classified 124 patients with prostate cancer without bone metastasis who received ADT into high- and low-risk groups using the JSBMR CTIBL algorithm. Comparisons were made with the period to incident vertebral fracture and the existing International Osteoporosis Foundation (IOF) classification.
The median age was 74 years; the median observation period was 81 months. At 1, 3, 5, 7, and 9 years, the prevalence of incident vertebral fractures was, respectively, 3.3%, 10.7%, 17.9%, 21.4%, and 31.2% in the entire population; 13%, 27%, 36%, 42%, and 58% in the high-risk group (19%); and 1%, 7%, 14%, 17%, and 25% in the low-risk group (81%). The hazard ratio between the two groups was 3.57 (p = 0.0004). Based on multivariate analysis, age, previous vertebral fracture and femoral neck bone density were significant risk factors for incidental vertebral fracture. The JSBMR had a hazard ratio of 3.26 (p = 0.04) relative to 1.13 (p = 0.84) for the IOF, indicating the JSBMR classification performed better.
Taking preventive measures against fractures is necessary, including starting bone-modifying agents early in patients with a high fracture risk. The JSBMR CTIBL manual may be useful for this purpose.
前列腺癌的去势治疗(ADT)会导致癌症治疗引起的骨丢失(CTIBL),使骨折风险增加 2-3 倍,并恶化预后。日本骨矿研究学会(JSBMR)于 2020 年制定了 CTIBL 治疗手册;然而,尚无研究验证其在接受 ADT/CTIBL 前列腺癌治疗的患者中的应用。
本研究使用 JSBMR CTIBL 算法将 124 例无骨转移的接受 ADT 的前列腺癌患者分为高风险和低风险组。并与现有的国际骨质疏松基金会(IOF)分类进行比较。
中位年龄为 74 岁;中位观察期为 81 个月。在整个人群中,1、3、5、7 和 9 年时,新发椎体骨折的患病率分别为 3.3%、10.7%、17.9%、21.4%和 31.2%;高风险组(19%)分别为 13%、27%、36%、42%和 58%;低风险组(81%)分别为 1%、7%、14%、17%和 25%。两组之间的风险比为 3.57(p=0.0004)。多因素分析显示,年龄、既往椎体骨折和股骨颈骨密度是新发椎体骨折的显著危险因素。JSBMR 的风险比为 3.26(p=0.04),而 IOF 的风险比为 1.13(p=0.84),表明 JSBMR 分类效果更好。
有必要采取预防骨折的措施,包括对高骨折风险患者早期使用骨修饰剂。JSBMR CTIBL 手册可能对此有用。