首页> 外文期刊>Brain pathology >Anaplastic Oligodendroglial Tumors: Refining the Correlation among Histopathology, 1p 19q Deletion and Clinical Outcome in Intergroup Radiation Therapy Oncology Group Trial 9402.
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Anaplastic Oligodendroglial Tumors: Refining the Correlation among Histopathology, 1p 19q Deletion and Clinical Outcome in Intergroup Radiation Therapy Oncology Group Trial 9402.

机译:间变性少突神经胶质瘤:在组间放射疗法肿瘤学小组试验9402中完善组织病理学,1p 19q缺失与临床结果之间的相关性。

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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.
机译:组间放射疗法肿瘤学小组试验9402研究,化学疗法与放射疗法(PCV-RT)与单纯放射疗法和混合性间变性少突神经胶质瘤单独放射疗法的III期试验证实了1p 19q缺失的预后意义,并显示仅无进展生存(PFS)在PCV-plus-RT治疗的患者中延长,仅与1p 19q缺失有关。我们回顾了肿瘤的组织病理学,将115个被认为是少突胶质细胞瘤(CFO)经典的肿瘤与132个缺乏少突胶质细胞瘤(NCFO)经典特征的肿瘤分开,并评估了组织病理学和1p 19q状态与治疗和结果之间的关系。该研究表明:(i)CFO患者的总生存期(OS)明显长于NCFO患者(P <0.0001),且不受坏死影响。有和没有坏死的CFO患者的中位OS分别为6.6年和6.3年(OS对数P =不显着),而NCFO分别为1.9年和3.3年(OS对数P = 0.014)。 (ii)经典少突胶质细胞形态与1p 19q缺失高度相关,在80%的CFO中仅出现在13%的NCFO中。 (iii)在多变量分析中,经典的少突胶质形态和1p 19q缺失仍与PFS和OS显着相关。 (iv)与接受RT治疗的CFO相比,接受PCV加RT治疗的CFO患者表现出生存率增加的趋势(P = 0.08)。 PCV-plus-RT组未达到中位OS,RT组为6.3年。这些发现表明,经典的少突胶质细胞形态结合1p 19q缺失可能在将来预示化学疗法的反应和生存。

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