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脊柱转移瘤立体定向体部放疗前使用抗骨吸收药物与椎体压缩骨折发生率降低相关。

Antiresorptive Medications Prior to Stereotactic Body Radiotherapy for Spinal Metastasis are Associated with Reduced Incidence of Vertebral Body Compression Fracture.

作者信息

Patel Palak P, Esposito Edward P, Zhu Jiafeng, Chen Xuguang, Khan Majid, Kleinberg Lawrence, Lubelski Daniel, Theodore Nicholas, Lo Sheng-Fu Larry, Hun Lee Sang, Kebaish Khaled, Bydon Ali, Redmond Kristin J

机构信息

Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Department of Biostatistics, Johns Hopkins School of Public Health, Baltimore, MD, USA.

出版信息

Global Spine J. 2024 Jul;14(6):1778-1785. doi: 10.1177/21925682231156394. Epub 2023 Feb 7.

Abstract

STUDY DESIGN

Retrospective Cohort.

OBJECTIVE

Antiresorptive drugs are often given to minimize fracture risk for bone metastases, but data regarding optimal time or ability to reduce stereotactic body radiotherapy (SBRT)-induced fracture risk is limited. This study examines the association between antiresorptive use surrounding spinal SBRT and vertebral compression fracture (VCF) incidence to provide information regarding effectiveness and optimal timing of use.

METHODS

Patients treated with SBRT for spinal metastases at a single institution between 2009-2020 were included. Kaplan-Meier analysis was used to compare cumulative incidence of VCF for those taking antiresorptive drugs pre-SBRT, post-SBRT only, and none at all. Cox proportional hazards and Fine-Gray competing risk models were used to identify additional factors associated with VCF.

RESULTS

Of the 234 patients (410 vertebrae) analyzed, 49 (20.9%) were taking bisphosphonates alone, 42 (17.9%) were taking denosumab alone, and 25 (10.7%) were taking both. Kaplan-Meier analysis revealed a statistically significant lower VCF incidence for patients initiating antiresorptive drugs before SBRT compared to those taking none at all (4% vs 12% at 1 year post-SBRT, = .045; and 4% vs 23% at 2 years, = .008). On multivariate analysis, denosumab duration (HR: .87, = .378) or dose (HR: 1.00, = .644) as well as bisphosphonate duration (HR: .98, = .739) or dose (HR: .99, = .741) did not have statistical significance on VCF incidence.

CONCLUSION

Initiating antiresorptive agents before SBRT may reduce the risk of treatment-induced VCF. Antiresorptive drugs are underutilized in patients with spine metastases and may represent a useful intervention to minimize toxicity and improve long-term outcomes.

摘要

研究设计

回顾性队列研究。

目的

抗吸收药物常用于降低骨转移的骨折风险,但关于降低立体定向体部放疗(SBRT)所致骨折风险的最佳时间或能力的数据有限。本研究探讨脊柱SBRT前后抗吸收药物的使用与椎体压缩骨折(VCF)发生率之间的关联,以提供有关其有效性和最佳使用时间的信息。

方法

纳入2009年至2020年在单一机构接受脊柱转移瘤SBRT治疗的患者。采用Kaplan-Meier分析比较SBRT前服用抗吸收药物、仅在SBRT后服用抗吸收药物以及未服用抗吸收药物的患者的VCF累积发生率。使用Cox比例风险模型和Fine-Gray竞争风险模型确定与VCF相关的其他因素。

结果

在分析的234例患者(410个椎体)中,49例(20.9%)仅服用双膦酸盐,42例(17.9%)仅服用地诺单抗,25例(10.7%)两者都服用。Kaplan-Meier分析显示,与未服用抗吸收药物的患者相比,SBRT前开始使用抗吸收药物的患者VCF发生率在统计学上显著更低(SBRT后1年时分别为4%和12%,P = 0.045;2年时分别为4%和23%,P = 0.008)。多因素分析显示,地诺单抗的使用时长(风险比:0.87,P = 0.378)或剂量(风险比:1.00,P = 0.644)以及双膦酸盐的使用时长(风险比:0.98,P = 0.739)或剂量(风险比:0.99,P = 0.741)对VCF发生率均无统计学意义。

结论

在SBRT前开始使用抗吸收药物可能降低治疗引起的VCF风险。脊柱转移瘤患者对抗吸收药物的使用不足,其可能是一种有用的干预措施,可将毒性降至最低并改善长期预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ec/11268289/b4cbd5103bc2/10.1177_21925682231156394-fig1.jpg

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