Department of Neuroradiology, IRCCS San Raffaele Scientific Institute and Vita-Salute San Raffaele University, Via Olgettina 60, 20132 Milan, Italy.
Department of Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan and Vita-Salute San Raffaele University, Via Olgettina 60, 20132 Milan, Italy.
Eur J Radiol. 2021 Oct;143:109945. doi: 10.1016/j.ejrad.2021.109945. Epub 2021 Sep 2.
To investigate the role of quantitative muscle biomarkers assessed with skeletal muscle index at the third lumbar vertebra (L3-SMI) and temporal muscle thickness (TMT) in predicting progression-free and overall survival in patients with primary central nervous system lymphoma (PCNSL) undergoing first-line high-dose methotrexate-based chemotherapy.
L3-SMI and TMT were calculated on abdominal CT and brain high-resolution 3D-T1-weighted MR images, respectively, using predefined validated methods. Standardized sex-specific cut-off values were used to divide patients in different risk categories. Kaplan-Meier plots were calculated, and survival analysis was performed using log-rank tests, univariate, and multivariable Cox-regression models, calculating hazard ratios (HR) and 95% confidence intervals (CI), also adjusting for potential confounders (age, sex, and performance status).
Forty-three patients were included in this study. Median follow-up was 23 months (interquartile range 12-40); at median follow-up, rates of progression-free and overall survival for the cohort were 46% and 57%, respectively. Thirteen (30%) and 11 (26%) patients showed L3-SMI or TMT values below the predefined cut-offs. In Cox-regression multivariable analysis patients with low L3-SMI or TMT showed significantly worse progression-free (HR 4.40, 95% CI 1.66-11.61, p = 0.003; HR 4.40, 95% CI 1.68-11.49, p = 0.003, respectively) and overall survival (HR 3.16, 95% CI 1.09-9.11, p = 0.034; HR 4.93, 95% CI 1.78-13.65, p = 0.002, respectively) compared to patients with high L3-SMI or TMT.
Quantitative muscle mass evaluation assessed by both L3-SMI and TMT is a promising tool to identify PCNSL patients at high risk of negative outcome. Confirmatory studies on larger independent series are warranted.
探讨基于第三腰椎骨骼肌指数(L3-SMI)和颞肌厚度(TMT)的定量肌肉生物标志物在预测接受一线大剂量甲氨蝶呤为基础的化疗的原发性中枢神经系统淋巴瘤(PCNSL)患者无进展和总生存中的作用。
在腹部 CT 和脑高分辨率 3D-T1 加权 MR 图像上分别使用预先验证的方法计算 L3-SMI 和 TMT。使用标准化的性别特异性截断值将患者分为不同风险类别。计算 Kaplan-Meier 图,并使用对数秩检验、单变量和多变量 Cox 回归模型进行生存分析,计算危险比(HR)和 95%置信区间(CI),并调整潜在混杂因素(年龄、性别和表现状态)。
本研究共纳入 43 例患者。中位随访时间为 23 个月(四分位距 12-40);在中位随访时,该队列的无进展生存率和总生存率分别为 46%和 57%。13 例(30%)和 11 例(26%)患者的 L3-SMI 或 TMT 值低于预设的截断值。在 Cox 回归多变量分析中,低 L3-SMI 或 TMT 的患者无进展生存(HR 4.40,95%CI 1.66-11.61,p=0.003;HR 4.40,95%CI 1.68-11.49,p=0.003)和总生存(HR 3.16,95%CI 1.09-9.11,p=0.034;HR 4.93,95%CI 1.78-13.65,p=0.002)明显更差。
通过 L3-SMI 和 TMT 评估的定量肌肉质量评估是一种有前途的工具,可以识别出 PCNSL 患者中预后不良的高危人群。需要在更大的独立系列中进行验证性研究。