Shibahara Ichiyo, Sonoda Yukihiko, Shoji Takuhiro, Kanamori Masayuki, Saito Ryuta, Inoue Tomoo, Kawaguchi Tomohiro, Yamashita Yoji, Watanabe Takashi, Kumabe Toshihiro, Watanabe Mika, Suzuki Hiroyoshi, Tominaga Teiji
Department of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan (I.S., Y.S., T.S., M.K., R.S., T.I., T.K., Y.Y., T.T.); Department of Public Health, Tohoku University School of Medicine, Sendai, Japan (T.W.); Department of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan (T.K.); Pathological Division, Tohoku University Hospital, Sendai, Japan (M.W.); Department of Pathology, Sendai Medical Center, Sendai, Japan (H.S.).
Neuro Oncol. 2015 Jan;17(1):136-44. doi: 10.1093/neuonc/nou112. Epub 2014 Jun 23.
Diagnosis of WHO grade III anaplastic gliomas does not always correspond to its clinical outcome because of the isocitrate dehydrogenase (IDH) gene status. Anaplastic gliomas without IDH mutation result in a poor prognosis, similar to grade IV glioblastomas. However, the malignant features of anaplastic gliomas without IDH mutation are not well understood. The aim of this study was to examine anaplastic gliomas, in particular those without IDH mutation, with regard to their malignant features, recurrence patterns, and association with glioma stem cells.
We retrospectively analyzed 86 cases of WHO grade III anaplastic gliomas. Data regarding patient characteristics, recurrence pattern, and prognosis were obtained from medical records. We examined molecular alterations such as IDH mutation, 1p19q loss, TP53 mutation, MGMT promoter methylation, Ki67 labeling index, and CD133, SOX2, and NESTIN expression.
Of the 86 patients with anaplastic gliomas, 58 carried IDH mutation, and 40 experienced recurrence. The first recurrence was local in 25 patients and distant in 15. Patients without IDH mutation exhibited significantly higher CD133 and SOX2 expression (P = .025 and .020, respectively) and more frequent distant recurrence than those with IDH mutation (P = .022).
Patients with anaplastic gliomas without IDH mutation experienced distant recurrence and exhibited glioma stem cell markers, indicating that this subset may share some malignant characteristics with glioblastomas.
由于异柠檬酸脱氢酶(IDH)基因状态,世界卫生组织(WHO)III级间变性胶质瘤的诊断并不总是与其临床结果相符。无IDH突变的间变性胶质瘤预后较差,与IV级胶质母细胞瘤相似。然而,无IDH突变的间变性胶质瘤的恶性特征尚未完全明确。本研究的目的是研究间变性胶质瘤,特别是无IDH突变的间变性胶质瘤的恶性特征、复发模式以及与胶质瘤干细胞的关系。
我们回顾性分析了86例WHO III级间变性胶质瘤病例。从病历中获取患者特征、复发模式和预后等数据。我们检测了分子改变,如IDH突变、1p19q缺失、TP53突变、MGMT启动子甲基化、Ki67标记指数以及CD133、SOX2和NESTIN表达。
86例间变性胶质瘤患者中,58例携带IDH突变,40例复发。首次复发时,25例为局部复发,15例为远处复发。无IDH突变的患者CD133和SOX2表达显著更高(分别为P = 0.025和0.020),且远处复发比有IDH突变的患者更频繁(P = 0.022)。
无IDH突变的间变性胶质瘤患者发生远处复发并表现出胶质瘤干细胞标志物,表明该亚组可能与胶质母细胞瘤具有一些共同的恶性特征。