Shibahara Ichiyo, Shigeeda Ryota, Watanabe Takashi, Orihashi Yasushi, Tanihata Yoko, Fujitani Kazuko, Handa Hajime, Hyakutake Yuri, Toyoda Mariko, Inukai Madoka, Uemasu Kohei, Shinoda Mitsuhiro, Komai Hideto, Sato Sumito, Hide Takuichiro, Kumabe Toshihiro
Department of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Department of General Internal Medicine, JCHO Sendai Hospital, Sendai, Miyagi, Japan.
Neurooncol Adv. 2024 Oct 23;6(1):vdae180. doi: 10.1093/noajnl/vdae180. eCollection 2024 Jan-Dec.
Glioblastoma (GB) is known for its highly invasive nature. Images of butterfly GB (bGB) often illustrate this characteristic, but the molecular background and origins of bGB remain unknown.
We analyzed a cohort of 34 bGB patients from our dataset (K-cohort) and 46 bGB patients from publicly available datasets, including TCGA-GBM, CPTAC-GBM, IvyGAP, and UPENN-GBM.
In the K-cohort, the median age was 66 years, and molecular analyses revealed promoter mutations in 55.9% of cases, with no cases exhibiting , or mutations. Sequential radiological imaging from the K-cohort provided unique insights, showing one case originating in the corpus callosum (CC) and 3 cases originating in the cerebral hemisphere before developing into bGB. Multi-regional sampling supported a mutational trajectory from the hemisphere to the CC. These observations indicate the presence of 2 distinct radiological origins for bGB. Consequently, we classified cases into CC-type and Hemispheric-type based on the tumor volume ratio within the CC. This subgrouping was clinically meaningful; the CC-type is an independent poor prognostic factor for overall survival, with a hazard ratio of 1.8 (95% confidence interval 1.1-3.0, = .033), and is molecularly distinct by a higher frequency of methylated p ( = .0039) compared to the Hemispheric-type.
Our results highlight that the radiological features of bGB are not homogenous and can indicate 2 potential subtypes based on their origins. Further studies are mandatory, but CC-type and Hemispheric-type exhibit distinct clinical backgrounds, outcomes, and molecular features.
胶质母细胞瘤(GB)以其高度侵袭性而闻名。蝴蝶状胶质母细胞瘤(bGB)的图像常常体现出这一特征,但bGB的分子背景和起源仍不清楚。
我们分析了来自我们数据集(K队列)的34例bGB患者以及来自公开可用数据集(包括TCGA-GBM、CPTAC-GBM、IvyGAP和UPENN-GBM)的46例bGB患者。
在K队列中,中位年龄为66岁,分子分析显示55.9%的病例存在启动子突变,没有病例表现出 、 或 突变。来自K队列的连续放射影像学检查提供了独特的见解,显示1例起源于胼胝体(CC),3例在发展为bGB之前起源于脑半球。多区域采样支持从半球到CC的突变轨迹。这些观察结果表明bGB存在两种不同的放射学起源。因此,我们根据CC内的肿瘤体积比将病例分为CC型和半球型。这种亚组分类具有临床意义;CC型是总生存期的独立不良预后因素,风险比为1.8(95%置信区间1.1 - 3.0, = 0.033),并且与半球型相比,甲基化p的频率更高,在分子上具有明显差异( = 0.0039)。
我们的结果强调,bGB的放射学特征并非同质,并且根据其起源可指示两种潜在亚型。必须进行进一步研究,但CC型和半球型表现出不同的临床背景、结局和分子特征。