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伴有 IDH 突变的低级别胶质瘤患者的癫痫发作。

Seizures in patients with IDH-mutated lower grade gliomas.

机构信息

Department of Neurosurgery, Sahlgrenska University Hospital, Blå Stråket 5, 41345, Gothenburg, Sweden.

Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Göteborg, Sweden.

出版信息

J Neurooncol. 2022 Nov;160(2):403-411. doi: 10.1007/s11060-022-04158-6. Epub 2022 Oct 18.

Abstract

PURPOSE

Most patients with Lower Grade Gliomas (LGG) present with epileptic seizures. Since the advent of molecular diagnostics, more homogenous sub-entities have emerged, including the isocitrate dehydrogenase-mutated (IDH-mutated) astrocytomas and 1p19q-codeleted oligodendrogliomas. We aimed to describe the occurrence of seizures in patients with molecularly defined LGG pre- and postoperatively and to analyze factors affecting seizure status postoperatively.

METHODS

A population-based cohort of 130 adult patients with IDH-mutated WHO grade 2 or 3 astrocytomas and oligodendrogliomas was assessed pertaining to seizure burden before and after surgery.

RESULTS

Fifty-four (79.4%) patients with astrocytoma and 45 (72.6%) patients with oligodendroglioma had a history of seizures before surgery. At 12 months postoperatively, 51/67 (76.1%) patients with astrocytoma and 47/62 (75.8%) patients with oligodendrogliomas were seizure free. In a multivariable logistic regression analysis, lower extent of resection (EOR) (OR 0.98; 95% CI 0.97-1.00, p = 0.01) and insular tumor location (OR 5.02; 95% CI 1.01-24.87, p = 0.048) were associated with presence of seizures within 1 year postoperatively in the entire LGG cohort. In sub-entities, EOR was in a similar manner associated with seizures postoperatively in astrocytomas (OR 0.98; 95% CI 0.96-0.99, p < 0.01) but not in oligodendrogliomas (p = 0.34).

CONCLUSION

Our results are well in line with data published for non-molecularly defined LGG with a large proportion of patients being seizure free at 1 year postoperative. Better seizure outcome was observed with increased EOR in astrocytomas, but this association was absent in oligodendrogliomas.

摘要

目的

大多数低级别胶质瘤(LGG)患者都伴有癫痫发作。自从分子诊断出现以来,更同质的亚实体已经出现,包括异柠檬酸脱氢酶突变(IDH 突变)星形细胞瘤和 1p19q 缺失的少突胶质细胞瘤。我们旨在描述分子定义的 LGG 患者术前和术后癫痫发作的发生情况,并分析影响术后癫痫状态的因素。

方法

对 130 名 IDH 突变的成人 2 级或 3 级星形细胞瘤和少突胶质细胞瘤患者进行了一项基于人群的队列评估,内容包括手术前后的癫痫发作负担。

结果

54 名星形细胞瘤(79.4%)和 45 名少突胶质细胞瘤(72.6%)患者术前有癫痫发作史。术后 12 个月时,67 名星形细胞瘤患者中有 51 名(76.1%)和 62 名少突胶质细胞瘤患者中有 47 名(75.8%)无癫痫发作。在多变量逻辑回归分析中,较低的肿瘤切除程度(EOR)(OR 0.98;95%CI 0.97-1.00,p=0.01)和岛叶肿瘤位置(OR 5.02;95%CI 1.01-24.87,p=0.048)与整个 LGG 队列术后 1 年内癫痫发作有关。在亚实体中,EOR 也以类似的方式与星形细胞瘤术后的癫痫发作相关(OR 0.98;95%CI 0.96-0.99,p<0.01),但与少突胶质细胞瘤无关(p=0.34)。

结论

我们的结果与非分子定义的 LGG 的数据非常吻合,其中很大一部分患者在术后 1 年无癫痫发作。星形细胞瘤中 EOR 越高,癫痫发作的预后越好,但在少突胶质细胞瘤中则没有这种关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8f3/9722876/0405491fe638/11060_2022_4158_Fig1_HTML.jpg

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