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双膦酸盐与地舒单抗预防伴骨转移的晚期癌症病理性骨折:一项随机对照试验的荟萃分析。

Bisphosphonates Versus Denosumab for Prevention of Pathological Fracture in Advanced Cancers With Bone Metastasis: A Meta-analysis of Randomized Controlled Trials.

机构信息

From the Division of Orthopaedic Surgery, McGill University, Montreal, Quebec, Canada.

出版信息

J Am Acad Orthop Surg Glob Res Rev. 2020 Aug;4(8):e20.00045. doi: 10.5435/JAAOSGlobal-D-20-00045.

DOI:10.5435/JAAOSGlobal-D-20-00045
PMID:32769706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7418898/
Abstract

BACKGROUND

Metastasis to the bone is one of the most common complications associated with advanced cancer. Patients with bone metastases are at risk of devastating skeletal related events, including pathological fractures.

PURPOSE

The aim of this study was to analyze the efficacy of zoledronic acid (ZA) versus denosumab in the prevention of pathological fractures in patients with bone metastases from advanced cancers by evaluating all available randomized controlled trials (RCTs) on this subject.

METHODS

A systematic search of electronic databases (PubMed and MEDLINE) was performed to identify all published RCTs comparing ZA with denosumab in prevention of pathological fractures in bone metastases. Risk of bias of the studies was assessed. The primary outcomes evaluated were pathological fractures.

RESULTS

Four RCTs (7,320 patients) were included. Denosumab was superior to ZA in reducing the likelihood of pathological fractures, when all tumor types were combined (odds ratio [OR] 0.86, 95% confidence interval [CI], 0.74 to 0.99, P = 0.04). Denosumab was favored, although not statistically significant, over ZA in endodermal origin (breast and prostate) (OR 0.85, 95% CI, 0.68 to 1.05, P = 0.13) and mesodermal origin tumors (solid tumors and multiple myeloma) (OR 0.87, 95% CI, 0.71 to 1.06, P = 0.16).

DISCUSSION

Denosumab moderately reduces the likelihood of pathological fractures in comparison to ZA in patients with bone metastases with statistical significance. When pathological fractures were grouped by tumor origin (endodermal or mesodermal), no statistical difference was observed between denosumab and ZA. Further long-term studies are needed to confirm the effectiveness of these treatment regimens.

摘要

背景

转移到骨骼是晚期癌症最常见的并发症之一。患有骨转移的患者有发生严重骨骼相关事件的风险,包括病理性骨折。

目的

本研究旨在通过评估所有关于该主题的已发表随机对照试验(RCT),分析唑来膦酸(ZA)与地舒单抗在预防晚期癌症骨转移患者病理性骨折方面的疗效。

方法

系统搜索电子数据库(PubMed 和 MEDLINE),以确定所有比较 ZA 与地舒单抗预防骨转移病理性骨折的已发表 RCT。评估研究的偏倚风险。主要评估结果为病理性骨折。

结果

共纳入 4 项 RCT(7320 例患者)。当所有肿瘤类型合并时,地舒单抗在降低病理性骨折的可能性方面优于 ZA(优势比 [OR] 0.86,95%置信区间 [CI] 0.74 至 0.99,P = 0.04)。尽管统计学上无显著差异,但地舒单抗在起源于内胚层(乳腺和前列腺)(OR 0.85,95%CI 0.68 至 1.05,P = 0.13)和中胚层起源肿瘤(实体瘤和多发性骨髓瘤)(OR 0.87,95%CI 0.71 至 1.06,P = 0.16)方面优于 ZA。

讨论

与 ZA 相比,地舒单抗可适度降低骨转移患者病理性骨折的可能性,具有统计学意义。当根据肿瘤起源(内胚层或中胚层)对病理性骨折进行分组时,地舒单抗与 ZA 之间未观察到统计学差异。需要进一步的长期研究来证实这些治疗方案的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/855ab5f9501a/jagrr-4-e20.00045-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/fcb53714ab19/jagrr-4-e20.00045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/b3895d54e00f/jagrr-4-e20.00045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/b3d13d69265f/jagrr-4-e20.00045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/3ac23a6a7d6d/jagrr-4-e20.00045-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/855ab5f9501a/jagrr-4-e20.00045-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/fcb53714ab19/jagrr-4-e20.00045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/b3895d54e00f/jagrr-4-e20.00045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/b3d13d69265f/jagrr-4-e20.00045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/3ac23a6a7d6d/jagrr-4-e20.00045-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/794f/7418898/855ab5f9501a/jagrr-4-e20.00045-g005.jpg

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