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长期前列腺癌管理过程中与药物相关的颌骨坏死的累积发生率和风险因素。

Cumulative incidence and risk factors for medication-related osteonecrosis of the jaw during long-term prostate cancer management.

机构信息

Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.

出版信息

Sci Rep. 2024 Jun 11;14(1):13451. doi: 10.1038/s41598-024-64440-7.

Abstract

Bone-modifying agents (BMA) are extensively used in treating patients with prostate cancer with bone metastases. However, this increases the risk of medication-related osteonecrosis of the jaw (MRONJ). The safety of long-term BMA administration in clinical practice remains unclear. We aimed to determine the cumulative incidence and risk factors of MRONJ. One hundred and seventy-nine patients with prostate cancer with bone metastases treated with BMA at our institution since 2008 were included in this study. Twenty-seven patients (15%) had MRONJ during the follow-up period (median, 19 months; interquartile range, 9-43 months). The 2-year, 5-year, and 10-year cumulative MRONJ incidence rates were 18%, 27%, and 61%, respectively. Multivariate analysis identified denosumab use as a risk factor for MRONJ, compared with zoledronic acid use (HR 4.64, 95% CI 1.93-11.1). Additionally, BMA use at longer than one-month intervals was associated with a lower risk of MRONJ (HR 0.08, 95% CI 0.01-0.64). Furthermore, six or more bone metastases (HR 3.65, 95% CI 1.13-11.7) and diabetes mellitus (HR 5.07, 95% CI 1.68-15.2) were risk factors for stage 2 or more severe MRONJ. MRONJ should be considered during long-term BMA administration in prostate cancer patients with bone metastases.

摘要

骨修饰剂(BMA)广泛用于治疗前列腺癌伴骨转移的患者。然而,这会增加药物相关性下颌骨坏死(MRONJ)的风险。BMA 在临床实践中的长期应用安全性仍不清楚。我们旨在确定 MRONJ 的累积发病率和危险因素。本研究纳入了自 2008 年以来在我院接受 BMA 治疗的 179 例前列腺癌伴骨转移患者。在随访期间,27 例(15%)患者发生 MRONJ(中位数,19 个月;四分位距,9-43 个月)。2 年、5 年和 10 年的累积 MRONJ 发生率分别为 18%、27%和 61%。多变量分析发现与唑来膦酸相比,地舒单抗的使用是 MRONJ 的危险因素(HR 4.64,95%CI 1.93-11.1)。此外,BMA 间隔超过 1 个月使用与 MRONJ 的风险较低相关(HR 0.08,95%CI 0.01-0.64)。此外,6 个或更多骨转移(HR 3.65,95%CI 1.13-11.7)和糖尿病(HR 5.07,95%CI 1.68-15.2)是 2 期或更严重 MRONJ 的危险因素。在前列腺癌伴骨转移患者长期 BMA 治疗期间应考虑 MRONJ。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23f9/11167048/57b803f36091/41598_2024_64440_Fig1_HTML.jpg

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