Department of Nuclear Medicine, APHM, La Timone Hospital, Marseille, France.
Department of Nuclear Medicine & Nancyclotep Imaging Platform, CHRU Nancy, Lorraine University, Nancy, France.
Eur J Nucl Med Mol Imaging. 2017 Aug;44(8):1306-1311. doi: 10.1007/s00259-017-3668-6. Epub 2017 Mar 14.
The World Health Organization Classification of Tumors of the Central Nervous System has recently been updated by the integration of diagnostic and prognostic molecular parameters, giving pivotal attention to IDH mutation as a favourable factor. Amino acid PET is increasingly used in the management of gliomas, but its prognostic value is a matter of debate. The aim of this study was to assess the relationship between IDH mutation and F-FDOPA uptake on PET in newly diagnosed gliomas.
A total of 43 patients, presenting with diffuse astrocytic and oligodendroglial grade II and III gliomas, reclassified according to the 2016 WHO classification of tumours of the CNS, were retrospectively included. They had all undergone F-FDOPA PET at an initial stage before surgery and histological diagnosis. F-FDOPA uptake values were compared between patients with and without IDH mutation in terms of maximum standardized uptake value (SUVmax) ratios between tumour and normal contralateral brain (T/N), and between tumour and striatum (T/S).
Patients with IDH mutation showed higher F-FDOPA T/N SUVmax ratios (1.6 vs. 1.2) and T/S SUVmax ratios (0.9 vs. 0.6) than patients without IDH mutation (p < 0.05).
This study showed paradoxically higher F-FDOPA uptake in diffuse grade II and III gliomas with IDH mutation. Despite evident interest in the management of gliomas, and especially in relation to posttherapy evaluation, our findings raise the question of the prognostic value of F-FDOPA uptake on PET uptake in this group of patients. This may be related to differences in amino acid integration, metabolism, or cell differentiation.
世界卫生组织(WHO)中枢神经系统肿瘤分类最近通过纳入诊断和预后分子参数进行了更新,特别关注 IDH 突变作为有利因素。氨基酸 PET 在胶质瘤的治疗中越来越多地被使用,但它的预后价值存在争议。本研究旨在评估新诊断的胶质瘤中 IDH 突变与 F-FDOPA 摄取之间的关系。
共纳入 43 例患者,这些患者均表现为弥漫性星形细胞瘤和少突胶质细胞瘤 II 级和 III 级,根据 2016 年 CNS 肿瘤 WHO 分类进行了重新分类。所有患者在手术和组织学诊断前均进行了 F-FDOPA PET 检查。根据肿瘤与对侧正常脑(T/N)和肿瘤与纹状体(T/S)之间的最大标准化摄取比值(SUVmax),比较 IDH 突变患者和无 IDH 突变患者之间的 F-FDOPA 摄取值。
IDH 突变患者的 F-FDOPA T/N SUVmax 比值(1.6 比 1.2)和 T/S SUVmax 比值(0.9 比 0.6)均高于无 IDH 突变患者(p<0.05)。
本研究显示 IDH 突变的弥漫性 II 级和 III 级胶质瘤的 F-FDOPA 摄取反而更高。尽管人们对胶质瘤的治疗,尤其是与治疗后评估有关的治疗非常感兴趣,但我们的发现提出了 F-FDOPA 在这组患者中的摄取对 PET 摄取的预后价值的问题。这可能与氨基酸整合、代谢或细胞分化的差异有关。