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疼痛性脊柱转移瘤的射频消融:一项系统评价

Radiofrequency Ablation of Painful Spinal Metastasis: A Systematic Review.

作者信息

Scaggiante Jacopo, Marsico Salvatore, Alexandre Andrea, Gaudino Simona, Ferrante Monica, Caronna Riccardo, Squillaci Ettore, Valente Iacopo, Garignano Giuseppe, D'Argento Francesco, De Leacy Reade, Pedicelli Alessandro

机构信息

Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico "A. Gemelli" IRCCS, 00168 Rome, Italy.

Unità Operativa Complessa di Diagnostica per Immagini e Radiologia Interventistica, Ospedale Isola Tiberina-Gemelli Isola, 00186 Rome, Italy.

出版信息

Curr Oncol. 2025 May 23;32(6):301. doi: 10.3390/curroncol32060301.

Abstract

OBJECTIVE

To systematically evaluate the effectiveness and safety of radiofrequency ablation (RFA) for managing pain caused by spinal metastases. This review aimed to consolidate evidence on RFA's analgesic efficacy and associated risks to inform clinical practice in palliative cancer care.

METHODS

A systematic review adhering to PRISMA guidelines was conducted. Databases were searched for studies evaluating RFA for spinal metastases pain. Inclusion criteria specified: randomized or non-randomized studies (prospective/retrospective); ≥3 adult patients; RFA used alone or combined with other treatments; reported pre- and post-RFA pain assessments; English language publication. Data extracted included patient demographics, primary tumor type, lesion location, pain scores (e.g., NRS/VAS), and complications. Pain response was assessed using definitions including the International Consensus Pain Response Endpoints (ICPRE) and definitions for moderate (≥2-point reduction) and high (≥4-point reduction) effectiveness.

RESULTS

This review included 33 studies, totaling 1336 patients (53.7% female) and 1787 treated lesions. The majority (85%) of studies reported highly effective pain management (≥4-point pain score reduction). The remaining 15% showed moderate effectiveness (≥2-point reduction). All studies reported achieving at least a partial pain response per ICPRE criteria. Mean pain scores decreased significantly from baseline (7.56/10) within 24-72 h (3.65) and remained low at 4 weeks (2.99), 12 weeks, and 24 weeks (both 2.70). Common primary cancers were lung (27.6%), breast (26.2%), and genitourinary (11.3%). Lesions were primarily in the thoracic (47.9%) and lumbar spine (47.3%). Crucially, no life-threatening (grade IV-V) complications occurred. The overall rate of grade I-III complications was low at 2.11%.

LIMITATIONS

This systematic review is limited by its study-level nature, preventing detailed subgroup analyses regarding specific metastasis characteristics or the impact of complementary therapies.

CONCLUSIONS

This systematic review suggests that RFA is a safe and effective treatment for pain control in patients with spinal metastases. It provides both rapid (within 24 h) and durable mid-term (up to 24 weeks) analgesia. The favorable safety profile, with a low complication rate, supports RFA as a valuable complimentary option within the multidisciplinary palliative management of painful spinal secondary tumors. Future randomized-controlled studies may help to further define its role when associated with other treatments.

摘要

目的

系统评价射频消融术(RFA)治疗脊柱转移瘤所致疼痛的有效性和安全性。本综述旨在整合有关RFA镇痛效果及相关风险的证据,为姑息性癌症护理中的临床实践提供参考。

方法

按照PRISMA指南进行系统综述。检索数据库以查找评估RFA治疗脊柱转移瘤疼痛的研究。纳入标准规定:随机或非随机研究(前瞻性/回顾性);≥3例成年患者;单独使用RFA或与其他治疗联合使用;报告RFA前后的疼痛评估;英文发表。提取的数据包括患者人口统计学信息、原发肿瘤类型、病变部位、疼痛评分(如数字评分法/NRS、视觉模拟评分法/VAS)和并发症。使用包括国际共识疼痛反应终点(ICPRE)以及中度(疼痛评分降低≥2分)和高度(疼痛评分降低≥4分)有效性定义来评估疼痛反应。

结果

本综述纳入33项研究,共1336例患者(女性占53.7%)和1787个治疗病变。大多数(85%)研究报告疼痛管理效果显著(疼痛评分降低≥4分)。其余15%显示中度有效性(疼痛评分降低≥2分)。所有研究均报告根据ICPRE标准至少实现了部分疼痛缓解。平均疼痛评分在24 - 72小时内从基线(7.56/10)显著下降至(3.65),并在4周(2.99)、12周和24周(均为2.70)时保持较低水平。常见的原发癌为肺癌(27.6%)、乳腺癌(26.2%)和泌尿生殖系统癌(11.3%)。病变主要位于胸椎(47.9%)和腰椎(47.3%)。至关重要的是,未发生危及生命(IV - V级)的并发症。I - III级并发症的总体发生率较低,为2.11%。

局限性

本系统综述受限于其研究层面的性质,无法针对特定转移特征或辅助治疗的影响进行详细的亚组分析。

结论

本系统综述表明,RFA是治疗脊柱转移瘤患者疼痛控制的一种安全有效的方法。它能提供快速(24小时内)和持久的中期(长达24周)镇痛效果具有良好的安全性,并发症发生率低,支持RFA作为多学科姑息治疗疼痛性脊柱继发性肿瘤的一种有价值的辅助选择。未来的随机对照研究可能有助于进一步明确其与其他治疗联合使用时的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110c/12192184/3ff91031a5f5/curroncol-32-00301-g001.jpg

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