Department of Neurosurgery, Ehime University School of Medicine, 454 Shitsukawa, Toon, Ehime, 791-0295, Japan.
Department of Neurosurgery, Washoukai Sadamoto Hospital, 1-6-1 Takehara, Matsuyama, Ehime, 790-0052, Japan.
Neurosurg Rev. 2021 Feb;44(1):587-597. doi: 10.1007/s10143-020-01258-7. Epub 2020 Feb 15.
Glioblastoma multiforme (GBM) is largely due to glioma stem cells (GSCs) that escape from total resection of gadolinium (Gd)-enhanced tumor on MRI. The aim of this study is to identify the imaging requirements for maximum resection of GBM with infiltrating GSCs. We investigated the relationship of tumor imaging volume between MRI and C-methionine (Met)-PET and also the relationship between Met uptake index and tumor activity. In ten patients, tumor-to-contralateral normal brain tissue ratio (TNR) was calculated to evaluate metabolic activity of Met uptake areas which were divided into five subareas by the degrees of TNR. In each GBM, tumor tissue was obtained from subareas showing the positive Met uptake. Immunohistochemistry was performed to examine the tumor proliferative activity and existence of GSCs. In all patients, the volume of Met uptake area at TNR ≦ 1.4 was larger than that of the Gd-enhanced area. The Met uptake area at TNR 1.4 beyond the Gd-enhanced tumor was much wider in high invasiveness-type GBMs than in those of low invasiveness type, and survival was much shorter in the former than the latter types. Immunohistochemistry revealed the existence of GSCs in the area showing Met uptake at TNR 1.4 and no Gd enhancement. Areas at TNR > 1.4 included active tumor cells with relatively high Ki-67 labeling index. In addition, it was demonstrated that GSCs could exist beyond the border of Gd-enhanced tumor. Therefore, to obtain maximum resection of GBMs, including infiltrating GSCs, aggressive surgical excision that includes the Met-positive area at TNR 1.4 should be considered.
多形性胶质母细胞瘤(GBM)主要是由于神经胶质瘤干细胞(GSCs)逃避磁共振成像(MRI)上钆增强肿瘤的完全切除。本研究旨在确定具有浸润性 GSCs 的 GBM 最大切除的影像学要求。我们研究了 MRI 和 C-蛋氨酸(Met)-PET 之间肿瘤成像体积的关系,以及 Met 摄取指数与肿瘤活性之间的关系。在 10 例患者中,通过 TNR 将 Met 摄取区域分为五个亚区,计算肿瘤与对侧正常脑组织的比值(TNR),以评估 Met 摄取区域的代谢活性。在每个 GBM 中,均从 TNR 显示阳性 Met 摄取的亚区获得肿瘤组织。进行免疫组织化学检查以检查肿瘤增殖活性和 GSCs 的存在。在所有患者中,TNR ≦ 1.4 的 Met 摄取区域体积大于 Gd 增强区域的体积。TNR 1.4 超过 Gd 增强肿瘤的 Met 摄取区域在高侵袭性 GBM 中比在低侵袭性 GBM 中宽得多,前者的生存时间比后者短得多。免疫组织化学显示 TNR 1.4 处的 Met 摄取区域存在 GSCs,而无 Gd 增强。TNR > 1.4 的区域包括具有相对较高 Ki-67 标记指数的活跃肿瘤细胞。此外,还证明 GSCs 可以存在于 Gd 增强肿瘤的边界之外。因此,为了获得包括浸润性 GSCs 在内的 GBM 的最大切除,应考虑进行包括 TNR 1.4 处 Met 阳性区域的积极手术切除。