Doyle Patrick, Caplan Sarah, Klinger Neil, Shin Kee-Young, Groff Michael, Dillon-Martin Maeve, Johnson Thomas, Kang Heejoo, Perkins Teresia, Novack Claire, Spektor Alexander, Huynh Mai Anh, Kim Ellen, Tanguturi Shyam, Richards Cara, Xu Wenxin Vincent, Kozono David, Alkalay Ron, Hackney David, Balboni Tracy
Department of Radiation Oncology, Brigham & Women's Hospital, Boston, Massachusetts.
Department of Neurosurgery, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Adv Radiat Oncol. 2025 May 9;10(7):101803. doi: 10.1016/j.adro.2025.101803. eCollection 2025 Jul.
The Spinal Instability Neoplastic Score (SINS) is the most common method of assessing spine stability in the setting of spinal metastases. We sought to assess (1) the SINS score as a predictor of vertebral compression fracture (VCF), (2) the risk contributions of the 6 SINS individual factors, and (3) other contributors to fracture risk.
In total, 194 patients with 391 spinal lesions that had not previously been treated with vertebroplasty/kyphoplasty, radiation therapy (RT), or surgery were enrolled before RT and followed for new or worsened fracture.
A total of 187 patients who were treated to 361 vertebral levels underwent post-RT follow-up. Average follow-up time for patients on study was 9.4 months (range, 0.2-38.8 months). A total of 33 new or worsened fractures (9.1% of lesions followed) were observed, with an average time to fracture of 4.4 months (range, 0.1-27.8 months). Of all 6 SINS factors, 3 were found to be individually significantly associated with increased risk of fracture, these were: lesion location in L2-L4 [hazard ratio (HR) = 2.78, = .04], mixed or lytic appearance on computed tomography (mixed HR = 3.87, = .01, lytic HR = 2.68, = .02), and <50% vertebral collapse (HR = 3.52, < .01). SINS as a summated score was significantly associated with increased risk of fracture on multivariable analysis ( < .01). Use of bone-strengthening medications such as bisphosphonates was also significantly associated with decreased risk of fracture in multivariable analysis in stable (SINS ≤6) (HR = 0.10, = .03) and potentially unstable (SINS, 7-12) lesions (HR: 0.18, = .03).
These findings support that SINS is a useful tool for estimating VCF risk, with lesion location, metastasis bone morphology, and presence of <50% collapse being the strongest predictors. Additionally, findings suggest that bone-strengthening medications such as bisphosphonates may mitigate the risk of developing VCF after RT.
脊柱不稳定肿瘤评分(SINS)是评估脊柱转移瘤患者脊柱稳定性最常用的方法。我们旨在评估:(1)SINS评分作为椎体压缩骨折(VCF)预测指标的价值;(2)SINS六个个体因素对骨折风险的贡献;(3)骨折风险的其他影响因素。
共纳入194例患者的391处脊柱病变,这些病变此前未接受过椎体成形术/后凸成形术、放射治疗(RT)或手术治疗,在RT前入组并随访新发或加重的骨折情况。
共187例接受361个椎体水平治疗的患者接受了RT后随访。研究中患者的平均随访时间为9.4个月(范围0.2 - 38.8个月)。共观察到33例新发或加重骨折(占随访病变的9.1%),骨折平均发生时间为4.4个月(范围0.1 - 27.8个月)。在所有6个SINS因素中,发现3个因素分别与骨折风险增加显著相关,分别为:病变位于L2 - L4(风险比[HR] = 2.78,P = .04)、计算机断层扫描显示为混合或溶骨性表现(混合HR = 3.87,P = .01,溶骨HR = 2.68,P = .02)以及椎体塌陷<50%(HR = 3.52,P < .01)。在多变量分析中,SINS总分与骨折风险增加显著相关(P < .01)。在稳定(SINS≤6)(HR = 0.10,P = .03)和潜在不稳定(SINS为7 - 12)病变的多变量分析中,使用双膦酸盐等骨强化药物也与骨折风险降低显著相关(HR:0.18,P = .03)。
这些研究结果支持SINS是评估VCF风险的有用工具,病变位置、转移瘤骨形态以及塌陷<50%是最强的预测因素。此外,研究结果表明双膦酸盐等骨强化药物可能降低RT后发生VCF的风险。