Medical Oncology Department, University Hospital Reina Sofia, Cordoba, Spain.
Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Cordoba, Spain.
J Neurooncol. 2024 May;167(3):407-413. doi: 10.1007/s11060-024-04618-1. Epub 2024 Mar 27.
Palliative WBRT is the main treatment for multiple BMs. Recent studies report no benefit in survival after WBRT compared to palliative supportive care in patients (pts) with poor prognosis. A new era of systemic treatment strategies based on targeted therapies are improving the prognosis of patients with BMs. The purpose of this study is to develop a prognostic score in palliative pts with BMs who undergo WBRT in this new setting.
239 pts with BMs who received palliative WBRT between 2013-2022 in our center were analyzed retrospectively. The score was designed according to the value of the β coefficient of each variable with statistical significance in the multivariate model using Cox regression. Once the score was established, a comparison was performed according to Kaplan-Meier and was analyzed by log-rank test.
149 pts (62.3%) were male and median (m) age was 60 years. 139 (58,2%) were lung cancer and 35 (14,6%) breast cancer. All patients received 30Gys in 10 sessions. m overall survival (OS) was 3,74 months (ms). 37 pts (15,5%) had a specific target mutation. We found that 62 pts were in group < 4 points with mOS 6,89 ms (CI 95% 3,18-10,62), 84 in group 4-7 points with mOS 4,01 ms (CI 95% 3,40-4,62) and 92 pts in group > 7 points with mOS 2,72 ms (CI 95% 1,93-3,52) (p < 0,001).
METASNCore items are associated with OS and they could be useful to select palliative pts to receive WBRT. More studies are necessary to corroborate our findings.
姑息性 WBRT 是多发性脑转移瘤的主要治疗方法。最近的研究报告称,在预后不良的患者中,与姑息性支持治疗相比,WBRT 并未带来生存获益。基于靶向治疗的新的系统治疗策略正在改善脑转移瘤患者的预后。本研究旨在为在这一新环境下接受姑息性 WBRT 的脑转移瘤患者制定预后评分。
回顾性分析了 2013 年至 2022 年期间在本中心接受姑息性 WBRT 的 239 例脑转移瘤患者。该评分是根据多变量模型中具有统计学意义的每个变量的β系数值,采用 Cox 回归设计的。评分建立后,通过 Kaplan-Meier 进行比较,并通过对数秩检验进行分析。
149 例患者(62.3%)为男性,中位年龄为 60 岁。139 例(58.2%)为肺癌,35 例(14.6%)为乳腺癌。所有患者均接受 30Gys 共 10 次。总生存期(OS)为 3.74 个月(ms)。37 例(15.5%)存在特定的靶基因突变。我们发现,62 例患者为<4 分组,mOS 为 6.89 ms(95%CI 3.18-10.62),84 例患者为 4-7 分组,mOS 为 4.01 ms(95%CI 3.40-4.62),92 例患者为>7 分组,mOS 为 2.72 ms(95%CI 1.93-3.52)(p<0.001)。
METASNCore 项目与 OS 相关,它们可能有助于选择接受 WBRT 的姑息性患者。需要进一步研究来证实我们的发现。