Giannini Caterina, Burger Peter C, Berkey Brian A, Cairncross J Gregory, Jenkins Robert B, Mehta Minesh, Curran Walter J, Aldape Ken
Division of Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Brain Pathol. 2008 Jul;18(3):360-9. doi: 10.1111/j.1750-3639.2008.00129.x. Epub 2008 Mar 26.
Intergroup Radiation Therapy Oncology Group Trial 9402 study, a phase III trial of chemotherapy plus radiotherapy (PCV-plus-RT) vs. radiotherapy alone for pure and mixed anaplastic oligodendroglioma confirmed the prognostic significance of 1p 19q deletion and showed that only progression-free survival (PFS) was prolonged in PCV-plus-RT-treated patients and only in association with 1p 19q deletion. We reviewed tumor histopathology, separating 115 tumors deemed to be classic for oligodendroglioma (CFO) from 132 lacking classic features of oligodendroglioma (NCFO) and evaluated the relationship of histopathology and 1p 19q status to treatment and outcome. The study disclosed: (i) overall survival (OS) of patients with CFO was significantly longer than for patients with NCFO (P < 0.0001) and was not affected by necrosis. Median OS for CFO patients with and without necrosis was 6.6 and 6.3 years (OS log-rank P = not significant), respectively, in contrast to NCFO showing 1.9 and 3.3 years respectively (OS log-rank P = 0.014). (ii) Classic oligodendroglial morphology was highly associated with 1p 19q deletion, present in 80% of CFO and only in 13% of NCFO. (iii) On multivariate analysis, both classic oligodendroglial morphology and 1p 19q deletion remained significantly associated with PFS and OS. (iv) Patients with CFO treated with PCV-plus-RT showed a trend toward increased survival compared with CFO treated with RT (P = 0.08). Median OS was not reached in the PCV-plus-RT group and was 6.3 years in RT group. These findings suggest that classic oligodendroglial morphology combined with 1p 19q deletion may in the future be predictive of chemotherapeutic response and survival.
肿瘤放射治疗肿瘤学组(Radiation Therapy Oncology Group)的9402号试验,一项关于单纯性和混合性间变性少突胶质细胞瘤采用化疗加放疗(PCV联合放疗)与单纯放疗对比的III期试验,证实了1p 19q缺失的预后意义,并表明只有接受PCV联合放疗的患者无进展生存期(PFS)得以延长,且仅与1p 19q缺失相关。我们回顾了肿瘤组织病理学,将115例被认为是少突胶质细胞瘤典型病例(CFO)的肿瘤与132例缺乏少突胶质细胞瘤典型特征(NCFO)的肿瘤区分开来,并评估了组织病理学和1p 19q状态与治疗及预后的关系。该研究揭示:(i)CFO患者的总生存期(OS)显著长于NCFO患者(P < 0.0001),且不受坏死影响。有坏死和无坏死的CFO患者的中位OS分别为6.6年和6.3年(OS对数秩检验P = 无显著性差异),相比之下,NCFO患者分别为1.9年和3.3年(OS对数秩检验P = 0.014)。(ii)典型的少突胶质细胞形态与1p 19q缺失高度相关,在80%的CFO中存在,而在NCFO中仅为13%。(iii)多因素分析显示,典型的少突胶质细胞形态和1p 19q缺失均与PFS和OS显著相关。(iv)接受PCV联合放疗的CFO患者与接受放疗的CFO患者相比,生存有增加趋势(P = 0.08)。PCV联合放疗组未达到中位OS,放疗组为6.3年。这些发现表明,典型的少突胶质细胞形态与1p