Mayo Clinic, Cannaday 2-E, Jacksonville, FL 32224, USA.
J Neurooncol. 2011 Aug;104(1):253-9. doi: 10.1007/s11060-010-0476-2. Epub 2010 Dec 12.
Glioblastomas (GBM) may originate de novo (primary), or following transformation from a lower grade glioma (secondary), and it has been postulated that these tumors may have different biological behaviors. We performed a correlative analysis involving 204 patients with glioma treated prospectively on NCCTG clinical trials. Central pathology review of tumor tissues taken at the time of initial diagnosis and at recurrence were performed in all patients. Tumors progressed from low (WHO grade 2) to high (grade 3-4) at recurrence in 45% low grade oligodendroglioma patients, in 70% with low grade oligoastrocytoma, and 74% with low grade astrocytoma (P = 0.031). Median overall survival (OS) from initial diagnosis varied by histology: oligodendroglioma, 8.8 years; (95% CI 5.7-10.2); oligoastrocytoma, 4.4 years (95% CI 3.5-5.6); astrocytoma grade 2 3.1 years (astrocytoma grade 2-4, 2.1 years) (95% CI 1.7-2.5, P < 0.001). Mean time to recurrence (TTR) also varied between patients with de novo GBM, those secondary GBM, and those that remained non-GBM at recurrence (1.1 ± 1.1 vs. 2.9 ± 1.8 vs. 4.0 ± 2.9 years, respectively, P < 0.001). Median OS from time of recurrence also varied between these three categories (0.7 years, 95% CI: 0.5-1.1 vs. 0.6 years, CI: 0.5-1.0 vs. 1.4 years, 95% CI: 1.1-2.0, respectively) (P < 0.001). At time of relapse, transformation to higher grade is frequent in low grade pure and mixed astrocytomas, but is observed in less than half of those with low grade oligodendroglioma. From time of recurrence, OS was not significantly different for those with primary versus secondary GBM, and it may thus be reasonable include patients with secondary GBM in clinical therapeutic trials for recurrent disease.
胶质母细胞瘤(GBM)可能是从头发生长(原发性),也可能是从低级别胶质瘤(继发性)转化而来,有人提出这些肿瘤可能具有不同的生物学行为。我们对前瞻性接受 NCCTG 临床试验治疗的 204 名胶质瘤患者进行了一项相关性分析。对所有患者的初始诊断时和复发时的肿瘤组织进行了中心病理复查。在低级别少突胶质细胞瘤患者中,45%的肿瘤在复发时从低级别进展为高级别(WHO 分级 3-4),在低级别少突星形细胞瘤患者中为 70%,在低级别星形细胞瘤患者中为 74%(P=0.031)。从初始诊断到复发的中位总生存期(OS)因组织学而异:少突胶质细胞瘤为 8.8 年(95%CI 5.7-10.2);少突星形细胞瘤为 4.4 年(95%CI 3.5-5.6);星形细胞瘤 2 级为 3.1 年(星形细胞瘤 2-4 级为 2.1 年)(95%CI 1.7-2.5,P<0.001)。新发 GBM、继发 GBM 和复发时仍为非 GBM 的患者之间的平均复发时间(TTR)也存在差异(分别为 1.1±1.1 年、2.9±1.8 年和 4.0±2.9 年,P<0.001)。从复发时间开始的中位 OS 也在这三个类别之间存在差异(0.7 年,95%CI:0.5-1.1 年、0.6 年,95%CI:0.5-1.0 年和 1.4 年,95%CI:1.1-2.0 年,分别)(P<0.001)。在复发时,低级别纯和混合星形细胞瘤中向高级别转化很常见,但在低级别少突胶质细胞瘤中不到一半的患者发生这种转化。从复发时间来看,原发性与继发性 GBM 患者的 OS 无显著差异,因此将继发性 GBM 患者纳入复发性疾病的临床治疗试验可能是合理的。