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地诺单抗剂量与拔牙对乳腺癌骨转移患者颌骨药物相关性骨坏死的影响

Denosumab Dosage and Tooth Extraction Predict Medication-Related Osteonecrosis of the Jaw in Patients with Breast Cancer and Bone Metastases.

作者信息

Yokoo Suguru, Kubo Shinichiro, Yamamoto Daisuke, Ikeda Masahiko, Yamashita Tetsumasa, Yoshikawa Kumiko, Mese Hiroshi, Ohara Sakiko

机构信息

Orthopedic Surgery, Fukuyama City Hospital, Fukuyama 721-8511, Japan.

Breast and Thyroid Surgery, Fukuyama City Hospital, Fukuyama 721-8511, Japan.

出版信息

Cancers (Basel). 2025 Jul 4;17(13):2242. doi: 10.3390/cancers17132242.

DOI:10.3390/cancers17132242
PMID:40647539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12249028/
Abstract

: Prolonged use of denosumab in patients with metastatic breast cancer has raised concerns about the development of medication-related osteonecrosis of the jaw (MRONJ). However, the threshold at which the risk increases remains unclear. : This retrospective cohort study analyzed patients with breast cancer and bone metastases who received denosumab between May 2012 and August 2024. Associations between cumulative denosumab administration and MRONJ were evaluated using univariate and multivariate logistic regression analyses. A receiver operating characteristic (ROC) analysis was used to determine the optimal cutoff for cumulative doses. : MRONJ developed in 101 patients (31.2%). Multivariate analysis identified cumulative denosumab administration (odds ratio [OR]: 1.05, 95% confidence interval [CI]: 1.03-1.06; < 0.001) and a history of tooth extraction (OR: 4.40, 95% CI: 2.23-8.71; < 0.001) as independent risk factors for MRONJ. ROC analysis determined an optimal cutoff of 32 cumulative doses, with an area under the curve of 0.83 (95% CI: 0.78-0.88; < 0.0001). : Cumulative denosumab administration and history of tooth extraction were independent risk factors for MRONJ in patients with breast cancer and bone metastases. The risk of MRONJ increased after 32 cumulative doses, providing a clinically actionable threshold for risk assessment and patient monitoring.

摘要

在转移性乳腺癌患者中长时间使用地诺单抗引发了人们对药物相关性颌骨坏死(MRONJ)发生的担忧。然而,风险增加的阈值仍不明确。

这项回顾性队列研究分析了2012年5月至2024年8月期间接受地诺单抗治疗的乳腺癌和骨转移患者。使用单因素和多因素逻辑回归分析评估地诺单抗累积给药与MRONJ之间的关联。采用受试者工作特征(ROC)分析来确定累积剂量的最佳截断值。

101例患者(31.2%)发生了MRONJ。多因素分析确定地诺单抗累积给药(比值比[OR]:1.05,95%置信区间[CI]:1.03 - 1.06;P < 0.001)和拔牙史(OR:4.40,95% CI:2.23 - 8.71;P < 0.001)是MRONJ的独立危险因素。ROC分析确定最佳截断值为32次累积剂量,曲线下面积为0.83(95% CI:0.78 - 0.88;P < 0.0001)。

地诺单抗累积给药和拔牙史是乳腺癌和骨转移患者发生MRONJ的独立危险因素。累积剂量达到32次后,MRONJ的风险增加,这为风险评估和患者监测提供了一个具有临床可操作性的阈值。

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本文引用的文献

1
A Comparison of the Efficacy and Safety of Denosumab and Zoledronic Acid in Patients with Bone Metastatic Breast Cancer Receiving CDK4/6 Inhibitor Therapy.在接受CDK4/6抑制剂治疗的骨转移性乳腺癌患者中地诺单抗与唑来膦酸的疗效和安全性比较
Medicina (Kaunas). 2025 Feb 19;61(2):360. doi: 10.3390/medicina61020360.
2
Immunotherapy in the Battle Against Bone Metastases: Mechanisms and Emerging Treatments.抗击骨转移中的免疫疗法:作用机制与新兴治疗方法
Pharmaceuticals (Basel). 2024 Nov 26;17(12):1591. doi: 10.3390/ph17121591.
3
Management of Medication-Related Osteonecrosis of the Jaw: An Overview of National and International Guidelines.
颌骨药物相关性骨坏死的管理:国家和国际指南概述
Br J Oral Maxillofac Surg. 2024 Dec;62(10):899-908. doi: 10.1016/j.bjoms.2024.08.008. Epub 2024 Sep 5.
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Trends in 5-year cancer survival disparities by race and ethnicity in the US between 2002-2006 and 2015-2019.2002-2006 年至 2015-2019 年期间美国按种族和民族划分的 5 年癌症生存率差距趋势。
Sci Rep. 2024 Sep 30;14(1):22715. doi: 10.1038/s41598-024-73617-z.
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Incidence of Medication-Related Osteonecrosis of the Jaw in Patients With Breast Cancer During a 20-Year Follow-Up: A Population-Based Multicenter Retrospective Study.一项基于人群的多中心回顾性研究:乳腺癌患者20年随访期间颌骨药物相关性骨坏死的发病率
J Clin Oncol. 2025 Jan 10;43(2):180-188. doi: 10.1200/JCO.24.00171. Epub 2024 Aug 20.
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How we manage medication-related osteonecrosis of the jaw.我们如何管理药物相关性颌骨坏死。
Eur J Med Res. 2024 Aug 2;29(1):402. doi: 10.1186/s40001-024-01912-6.
7
Cumulative incidence and risk factors for medication-related osteonecrosis of the jaw during long-term prostate cancer management.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。
Sci Rep. 2024 Jun 11;14(1):13451. doi: 10.1038/s41598-024-64440-7.
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Lung Cancer. 2024 Jun;192:107826. doi: 10.1016/j.lungcan.2024.107826. Epub 2024 May 22.
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