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辅助替莫唑胺化疗后胶质瘤患者 F-FET PET 与对比增强 MRI 早期治疗反应评估。

Early Treatment Response Assessment Using F-FET PET Compared with Contrast-Enhanced MRI in Glioma Patients After Adjuvant Temozolomide Chemotherapy.

机构信息

Department of Neurology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Germany.

Institute of Neuroscience and Medicine (INM-3, -4), Research Center Juelich, Juelich, Germany.

出版信息

J Nucl Med. 2021 Jul 1;62(7):918-925. doi: 10.2967/jnumed.120.254243. Epub 2020 Nov 6.

Abstract

The goal of this study was to compare the value of contrast-enhanced MRI and O-(2-[F]fluoroethyl)-l-tyrosine (F-FET) PET for response assessment in glioma patients after adjuvant temozolomide chemotherapy (TMZ). After biopsy or resection and completion of radiotherapy with concomitant TMZ, 41 newly diagnosed and histomolecularly characterized glioma patients (glioblastoma, 90%; age range, 20-79 y) were subsequently treated with adjuvant TMZ. MR and F-FET PET imaging were performed at baseline and after the second cycle of adjuvant TMZ. We obtained F-FET metabolic tumor volumes (MTVs) as well as mean and maximum tumor-to-brain ratios (TBR and TBR, respectively). Threshold values of F-FET PET parameters to predict outcome were established by receiver-operating-characteristic analyses using a median progression-free survival (PFS) of ≥ 9 mo and overall survival (OS) of ≥ 15 mo as reference. MRI response assessment was based on the Response Assessment in Neuro-Oncology (RANO) working group criteria. The predictive value of changes of F-FET PET and MRI parameters on survival was evaluated subsequently using univariate and multivariate survival estimates. After 2 cycles of adjuvant TMZ chemotherapy, a treatment-induced reduction of MTV and TBR predicted a significantly longer PFS and OS (both ≤ 0.03; univariate survival analyses) whereas RANO criteria were not significant ( > 0.05). Multivariate survival analysis revealed that TBR changes predicted a prolonged PFS ( = 0.012) and changes of MTV a prolonged OS ( = 0.005) independent of O-methylguanine-DNA-methyltransferase promoter methylation and other strong prognostic factors. Changes of F-FET PET parameters appear to be helpful for identifying responders to adjuvant TMZ early after treatment initiation.

摘要

本研究旨在比较对比增强 MRI 和 O-(2-[F]氟乙基)-L-酪氨酸 (F-FET) PET 对接受辅助替莫唑胺化疗 (TMZ) 的胶质瘤患者的反应评估价值。 在活检或切除后以及完成同步 TMZ 放疗后,41 名新诊断和组织分子特征明确的胶质瘤患者(胶质母细胞瘤,90%;年龄范围,20-79 岁)随后接受辅助 TMZ 治疗。在基线和辅助 TMZ 治疗的第二个周期后进行了 MR 和 F-FET PET 成像。我们获得了 F-FET 代谢肿瘤体积 (MTV) 以及平均和最大肿瘤与脑比 (TBR 和 TBR)。使用中位数无进展生存期 (PFS) ≥ 9 个月和总生存期 (OS) ≥ 15 个月作为参考,通过接收者操作特征分析确定 F-FET PET 参数的阈值值以预测结果。 MRI 反应评估基于神经肿瘤反应评估 (RANO) 工作组标准。随后使用单变量和多变量生存估计评估 F-FET PET 和 MRI 参数变化对生存的预测价值。 在接受辅助 TMZ 化疗 2 个周期后,MTV 和 TBR 的治疗诱导减少可显著预测更长的 PFS 和 OS(均 ≤ 0.03;单变量生存分析),而 RANO 标准无统计学意义(> 0.05)。多变量生存分析表明,TBR 变化可预测 PFS 延长( = 0.012),而 MTV 变化可预测 OS 延长( = 0.005),独立于 O-甲基鸟嘌呤-DNA-甲基转移酶启动子甲基化和其他强预后因素。 F-FET PET 参数的变化似乎有助于在治疗开始后早期识别对辅助 TMZ 的反应者。

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