首页> 美国卫生研究院文献>Neuro-Oncology >P10.24 Outcome evaluation of patients with newly diagnosed anaplastic gliomas treated in a single institution using a multimodal approach: review according to the new 2016 World Health Organization (WHO) classification system
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P10.24 Outcome evaluation of patients with newly diagnosed anaplastic gliomas treated in a single institution using a multimodal approach: review according to the new 2016 World Health Organization (WHO) classification system

机译:P10.24使用多模式方法在单个机构中治疗的新诊断的间变性神经胶质瘤患者的结果评估:根据新的2016年世界卫生组织(WHO)分类系统进行审查

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摘要

>Background: Anaplastic gliomas represent less than 10% of newly diagnosed primary brain tumors. In the last years, comprehensive and integrative genomic and molecular analysis led to identify biologic classes with clinically distinct behavior and to determine whether gliomas are more accurately defined by molecular status than by histological features. Based on this background we evaluated the outcome of patients with newly diagnosed anaplastic glioma treated in our institution reviewing this series in relation to the 2016 WHO classification suggestions. >Methods: This retrospective study included patients with newly diagnosed anaplastic gliomas underwent surgery plus adjuvant chemotherapy (CHT) alone or concomitant and adjuvant chemo-radiotherapy (CHTRT). Surgery was performed in all patients with the aim to maximally remove the tumor according with functional boundaries. The extent of resection (EOR) was defined as Complete resection(CR) in case of residual tumor volume lower than 1.0cm3, subtotal resection(SR) between 1.0cm3 and 10.0cm3 and partial resection(PR) greater than 10.0cm3. The adjuvant treatment proposed was CHT in case of young patients with oligodendroglial tumors, IDH-mutated and 1p/19q-codeleted, underwent CR; in all the other cases RT with concurrent and adjuvant TMZ was performed. The total RT dose prescribed was 60 Gy in 30 fractions. Three classes have been defined in relation to the molecular parameters: class I IDH mutated and 1p/19q codeleted tumors; class II IDH mutated and 1p/19q no codeleted tumors; class III IDH wild type tumors. Response was recorded using the Response Assessment in Neuro-Oncology (RANO) criteria. >Results: From January 2008 to May 2014, 123 patients were treated. According with histopathological features, 54 (43.9%) patients had diagnosis of AO, 36 (29.3%) of AOA, and 33 (26.8%) of AA. Considering molecular parameters, 69 (56.1%) patients were in class I, 39 (31.7%) in class II and 15 (12.2%) in class III. All patients underwent surgical resection; adjuvant chemotherapy alone with TMZ was performed in 51 (41,5%) patients and RT with concurrent and adjuvant TMZ in 72 (58.5%). The median follow up time for the whole cohort was 35.1 months (range 9.3-95.7 months) and 35.6 months (range 19.2-95.7 months) for the alive patients. The median PFS time and the 2, 3, 5 years PFS rate were 27 months, 65.5% 21.2%, 21.2%; the 2, 3, 5 years OS rate were 89.7%, 83.0%, 58.4%. On univariate and multivariate analysis factors conditioning survival were KPS, EOR, IDH1 mutation status, and presence of 1p-19q codeletion. >Conclusion: A stratification of patients by clinical and molecular features and a revision according with 2016 WHO classification of CNS tumors resulted more predictive and prognostic on outcome of anaplastic glioma patients. The treatment choice have to consider molecular assessment and, in our experience, the extent of surgical resection.
机译:>背景:间变性胶质瘤仅占新诊断的原发性脑肿瘤的不到10%。近年来,全面和综合的基因组和分子分析可确定具有临床不同行为的生物学类别,并确定胶质瘤是否由分子状态比由组织学特征更准确地定义。基于此背景,我们评估了我们机构中与2016年WHO分类建议相关的本系列研究的新诊断的间变性神经胶质瘤患者的结局。 >方法:这项回顾性研究纳入了刚诊断为间变性神经胶质瘤的患者,他们接受了手术加单独的辅助化疗(CHT)或辅助化疗和辅助放化疗(CHTRT)。在所有患者中均进行了手术,目的是根据功能边界最大程度地切除肿瘤。如果残余肿瘤体积小于1.0cm 3 ,则切除范围(EOR)定义为完全切除(CR),小肠切除(SR)介于1.0cm 3 之间10.0cm 3 和部分切除(PR)大于10.0cm 3 。对于年轻的IDH突变和1p / 19q小细胞编码的少突胶质细胞瘤患者,建议行CHT辅助治疗。在所有其他情况下,均进行了并发TMZ和辅助TMZ的RT。规定的总RT剂量为30馏分中的60 Gy。关于分子参数,已定义了三类:IDH I突变型和1p / 19q编码肿瘤。 II类IDH突变和1p / 19q无小肿瘤III类IDH野生型肿瘤。使用神经肿瘤反应评估(RANO)标准记录反应。 >结果:从2008年1月到2014年5月,共治疗123例患者。根据组织病理学特征,诊断为AO的患者54例(43.9%),诊断为AOA的患者36例(29.3%),诊断为AA的患者33例(26.8%)。考虑分子参数,I级患者为69(56.1%),II级患者为39(31.7%),III级患者为15(12.2%)。所有患者均接受手术切除;在51(41.5%)例患者中单独进行TMZ辅助化疗,在72例(58.5%)的患者中同时进行TMZ辅助化疗。整个队列的中位随访时间为35.1个月(9.3-95.7个月)和35.6个月(19.2-95.7个月)。 PFS时间中位数和2、3、5年PFS率分别为27个月,65.5%21.2%,21.2%; 2、3、5年的OS率分别为89.7%,83.0%,58.4%。在单因素和多因素分析因素中,条件存活率分别为KPS,EOR,IDH1突变状态和1p-19q编码缺失。 >结论:根据临床和分子特征对患者进行分层,并根据2016年WHO对CNS肿瘤的分类进行修订,可对变性性神经胶质瘤患者的预后做出更佳的预测和预后。治疗的选择必须考虑分子评估以及我们的经验,即手术切除的范围。

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