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骨转移导向治疗的多学科方法的最新进展:GEMO实践指南编写的综述与挑战性问题

State-of-the-art of multidisciplinary approach of bone metastasis-directed therapy: review and challenging questions for preparation of a GEMO practice guidelines.

作者信息

Mesny Emmanuel, Martz Nicolas, Stacoffe Nicolas, Clarençon Frédéric, Louis Matthias, Mansouri Nacer, Sirveaux François, Thureau Sébastien, Faivre Jean-Christophe

机构信息

Radiation Oncology Department, Hospices Civils de Lyon, CHLS, Lyon, France.

Radiation Oncology Department, Institut de Cancérologie de Lorraine-Alexis-Vautrin, Vandœuvre-Lès-Nancy, France.

出版信息

Cancer Metastasis Rev. 2025 Apr 12;44(2):45. doi: 10.1007/s10555-025-10262-6.

Abstract

Bone is a common secondary site of dissemination during the course of cancer. Bone metastases (BM) can be associated with skeletal-related events (SRE) such as disabling pain, hypercalcemia, and bone instability that leads to pathological fractures or spinal cord compression. SRE contribute to high morbidity as well as, mortality, and have a negative economic impact. Modern management of BM integrates focal treatments (such as radiotherapy, surgery, and interventional radiology), orthoses, and antiresorptive and systemic oncological treatment. The choice of a metastasis-directed therapy depends on the objective of the treatment, the patient characteristics, and the complete assessment of the bone lesion (pain, neurological risk, and instability). In the narrative review present herein, we aim to provide an updated summary of the literature, with description of the advantages and disadvantages of current and emerging strategies in the multimodal treatment of BM and, based on these data, an updated algorithm for the management of BM.

摘要

骨是癌症病程中常见的转移继发部位。骨转移(BM)可伴有骨相关事件(SRE),如致残性疼痛、高钙血症以及导致病理性骨折或脊髓压迫的骨不稳定。SRE会导致高发病率和死亡率,并产生负面的经济影响。BM的现代治疗整合了局部治疗(如放疗、手术和介入放射学)、矫形器以及抗吸收和全身性肿瘤治疗。转移导向治疗的选择取决于治疗目标、患者特征以及对骨病变(疼痛、神经风险和不稳定)的全面评估。在本文的叙述性综述中,我们旨在提供文献的最新总结,描述BM多模式治疗中当前和新兴策略的优缺点,并基于这些数据提供BM管理的更新算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00fd/11993453/bcda588b0b3d/10555_2025_10262_Fig1_HTML.jpg

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