[11C]-蛋氨酸 PET 在小儿低级别胶质瘤评估中的应用

IF 3.7 Q1 CLINICAL NEUROLOGY
Emily Y Kim, A. Vāvere, Scott E Snyder, J. Chiang, Yimei Li, T. Patni, I. Qaddoumi, T. E. Merchant, G. Robinson, Joseph Holtrop, Barry L. Shulkin, A. Bag
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引用次数: 0

摘要

[11C]-蛋氨酸 PET([11C]-MET-PET)主要用于评估成人脑肿瘤。虽然氨基酸 PET 示踪剂更常用于评估小儿脑肿瘤,但小儿低级别胶质瘤(pLGG)的 [11C]-MET-PET 成像数据却很少。本研究旨在探讨[11C]-MET-PET在评估pLGG中的作用。 18名新诊断的pLGG患者和26名既往接受过治疗的pLGG患者接受了[11C]-MET-PET检查,均符合纳入和排除标准。评估了肿瘤与脑摄取比(TBR)和代谢肿瘤体积(MTV)的诊断性能(新诊断 15 例;既往治疗 26 例)、治疗变化(新诊断 9 例;既往治疗 7 例)以及不同组织学(12 例)和分子标记物(7 例)的 pLGG 之间的差异。 [11C]-MET-PET诊断pLGG、新诊断pLGG和既往治疗pLGG的灵敏度,TBRmax和TBRpeak均为93%,TBRmean为76%,定性评估为95%。TBRmax在治疗后出现了统计学意义上的显著下降,而其他PET参数则呈下降趋势。与BRAF融合肿瘤相比,BRAFV600E突变肿瘤的TBRmax、TBRpeak和TBRmean中值略高。弥漫性星形细胞瘤的 TBRmax 中值和 TBRpeak 中值高于趋向性星形细胞瘤,但趋向性星形细胞瘤的 TBRmean 中值略高于弥漫性星形细胞瘤。不过,由于样本量较小,没有进行正式的统计分析。 我们的研究表明,[11C]-MET-PET 能可靠地描述新发和既往治疗过的 pLGG。我们的研究还表明,定量参数往往会随着治疗而降低,而且不同类型的 pLGG 之间可能存在差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[11C]-Methionine PET in the Evaluation of Pediatric Low-grade Gliomas
[11C]-Methionine PET ([11C]-MET-PET) is principally used for the evaluation of brain tumors in adults. Although amino acid PET tracers are more commonly used in evaluation of pediatric brain tumors, data on [11C]-MET-PET imaging of pediatric low-grade gliomas (pLGG) is scarce. This study aimed to investigate roles of [11C]-MET-PET in evaluation of pLGGs. Eighteen patients with newly diagnosed pLGG and twenty-six previously treated pLGG patients underwent [11C]-MET-PET met the inclusion and exclusion criteria. Tumor-to-brain uptake ratio (TBR) and metabolic tumor volumes (MTV) were assessed for diagnostic performances (newly diagnosed, 15; previously treated 26), change with therapy (newly diagnosed, 9; previously treated 7), and variability among different histology (n=12) and molecular markers (n=7) of pLGGs. The sensitivity of [11C]-MET-PET for diagnosing pLGG, newly diagnosed, and previously treated combined was 93% for both TBRmax and TBRpeak, 76% for TBRmean, and 95% for qualitative evaluation. TBRmax showed a statistically significant reduction after treatment, while other PET parameters showed a tendency to decrease. Median TBRmax, TBRpeak, and TBRmean values were slightly higher in the BRAFV600E mutated tumors compared to the BRAF fused tumors. Median TBRmax, and TBRpeak in diffuse astrocytomas were higher compared to pilocytic astrocytomas, but median TBRmean, was slightly higher in pilocytic astrocytomas. However, formal statistical analysis was not done due to the small sample size. Our study shows that [11C]-MET-PET reliably characterizes new and previously treated pLGGs. Our study also shows that quantitative parameters tend to decrease with treatment, and differences may exist between various pLGG types.
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CiteScore
6.20
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