Department of Neurosurgery, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0374, Japan.
Gene Analysis Center, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
J Neurooncol. 2024 Aug;169(1):39-50. doi: 10.1007/s11060-024-04687-2. Epub 2024 Jun 5.
This study investigated the factors influencing short-term survivors (STS) after gross total resection (GTR) in patients with IDH1 wild-type primary glioblastoma.
We analyzed five independent cohorts who underwent GTR, including 83 patients from Kitasato University (K-cohort), and four validation cohorts of 148 patients from co-investigators (V-cohort), 66 patients from the Kansai Molecular Diagnosis Network for the Central Nervous System tumors, 109 patients from the Cancer Genome Atlas, and 40 patients from the Glioma Longitudinal AnalySiS. The study defined STS as those who had an overall survival ≤ 12 months after GTR with subsequent radiation therapy, and concurrent and adjuvant temozolomide (TMZ).
The study included 446 patients with glioblastoma. All cohorts experienced unexpected STS after GTR, with a range of 15.0-23.9% of the cases. Molecular profiling revealed no significant difference in major genetic alterations between the STS and non-STS groups, including MGMT, TERT, EGFR, PTEN, and CDKN2A. Clinically, the STS group had a higher incidence of non-local recurrence early in their treatment course, with 60.0% of non-local recurrence in the K-cohort and 43.5% in the V-cohort.
The study revealed that unexpected STS after GTR in patients with glioblastoma is not uncommon and such tumors tend to present early non-local recurrence. Interestingly, we did not find any significant genetic alterations in the STS group, indicating that such major alterations are characteristics of GB rather than being reliable predictors for recurrence patterns or development of unexpected STS.
本研究调查了 IDH1 野生型原发性胶质母细胞瘤患者行大体全切除(GTR)后短期幸存者(STS)的影响因素。
我们分析了 5 个独立的接受 GTR 的队列,包括来自 Kitasato 大学的 83 名患者(K 队列),以及来自合作研究者的 4 个验证队列共 148 名患者(V 队列)、66 名来自关西中枢神经系统肿瘤分子诊断网络的患者、109 名来自癌症基因组图谱的患者和 40 名来自神经胶质瘤纵向分析的患者。本研究将 STS 定义为在 GTR 后接受放疗以及同期和辅助替莫唑胺(TMZ)治疗后总生存时间≤12 个月的患者。
本研究纳入了 446 名胶质母细胞瘤患者。所有队列在 GTR 后均出现了意外的 STS,病例比例为 15.0-23.9%。分子谱分析显示,STS 组和非 STS 组之间在主要遗传改变方面没有显著差异,包括 MGMT、TERT、EGFR、PTEN 和 CDKN2A。临床研究中,STS 组在治疗早期出现非局部复发的比例更高,K 队列中 60.0%的患者和 V 队列中 43.5%的患者发生非局部复发。
本研究表明,胶质母细胞瘤患者行 GTR 后出现意外的 STS 并不罕见,此类肿瘤往往表现为早期非局部复发。有趣的是,我们并未在 STS 组中发现任何显著的遗传改变,这表明这些主要改变是胶质母细胞瘤的特征,而不是复发模式或意外 STS 发展的可靠预测因素。