A series of 309 awake surgeries with transcortical approach for IDH-mutant low-grade glioma involving the insula: long-term onco-functional outcomes in 253 consecutive patients.

IF 3.5 2区 医学 Q1 CLINICAL NEUROLOGY
Hugues Duffau
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引用次数: 0

Abstract

Objective: In low-grade glioma (LGG), awake surgery (AS) with intraoperative functional mapping minimizes morbidity while increasing the extent of resection (EOR). However, the actual role of AS for insular LGG resection through the opercula is still debated. The aim of this study was to investigate the long-term results after AS via a transcortical approach in patients with LGG within the insula, and to compare outcomes between pure insular gliomas and gliomas also invading other lobes.

Methods: Patients who underwent AS with functional-based resection via the opercula performed by the author for an isocitrate dehydrogenase-mutant grade 2 glioma involving the insula were selected (June 2002-January 2024). Functional and oncological outcomes were analyzed by comparing pure insular gliomas (group 1) versus insular-centered gliomas also involving the frontal and/or temporal and/or parietal lobes (group 2).

Results: In this consecutive cohort, 309 ASs were achieved in 253 patients (132 men [52.2%], mean age 37.5 ± 9.5 years). Among 214 patients (84.5%) with epilepsy before surgery, 55 had intractable seizures (21.7%). The preoperative mean Karnofsky Performance Scale score was 93.1 ± 7.4, with 206 patients (81.4%) working before surgery. The series included 147 left-sided gliomas (58.1%), with a mean preoperative tumor volume for both sides of 70.1 ± 50.1 cm3 with 39 total tumors (15.4%) in group 1 and 214 total tumors (84.6%) in group 2. No patients except 2 (99.2%) had a permanent postoperative deficit (mean Karnofsky Performance Scale score 93 ± 6.6), with 199 patients returning to work (96.6%). Only 20 patients (7.9%) continued to suffer from intractable epilepsy. The mean EOR was 89.4% ± 8.4% (mean residual tumor volume: 9.6 ± 13.1 cm3). There were 166 astrocytomas (65.6%) and 87 oligodendrogliomas (34.4%). Fifty-three patients (20.9%) received immediate postoperative adjuvant therapy and 49 patients (19.3%) underwent subsequent AS. The mean follow-up was 7.1 ± 3.9 years, with an overall survival rate of 80.2% (203 patients were still alive at last evaluation). More patients had an incidental glioma in group 1 (p = 0.00009), whereas there was a higher rate of intractable seizures (p = 0.0019) and a greater tumor volume before surgery in group 2 (p < 0.00001). Nonetheless, the EOR and the rate of postoperative intractable seizures were similar in both groups, with more patients in group 2 resuming work (p = 0.001).

Conclusions: This is the largest homogeneous surgical experience of LGGs involving the insula that were resected through the opercula based on awake mapping. The results show a high percentage of functional preservation and return to work, with a high overall survival rate.

309例经皮质入路清醒手术治疗涉及脑岛的idh突变低级别胶质瘤:253例连续患者的长期非功能性结果
目的:在低级别胶质瘤(LGG)中,术中功能定位的清醒手术(AS)可以减少发病率,同时增加切除范围(EOR)。然而,AS在岛状LGG经包盖切除中的实际作用仍有争议。本研究的目的是通过经皮质入路研究脑岛内LGG患者AS后的长期结果,并比较单纯的脑岛胶质瘤和侵袭其他脑叶的胶质瘤的结果。方法:选择由作者对累及脑岛的异柠檬酸脱氢酶突变的2级胶质瘤进行AS功能切除的患者(2002年6月- 2024年1月)。通过比较单纯的岛状胶质瘤(第1组)和岛状中心胶质瘤(第2组),分析功能和肿瘤预后。结果:在该连续队列中,253例患者(男性132例[52.2%],平均年龄37.5±9.5岁)获得309例ASs。214例术前癫痫患者(84.5%)中,55例发生难治性癫痫发作(21.7%)。术前Karnofsky评分平均为93.1±7.4分,206例(81.4%)患者术前工作。左侧胶质瘤147例(58.1%),术前平均双侧肿瘤体积70.1±50.1 cm3, 1组共39例(15.4%),2组共214例(84.6%)。除2例(99.2%)患者术后出现永久性缺陷(Karnofsky Performance Scale平均评分93±6.6)外,199例患者恢复工作(96.6%)。只有20例(7.9%)患者继续患有顽固性癫痫。平均EOR为89.4%±8.4%(平均残余肿瘤体积:9.6±13.1 cm3)。星形细胞瘤166例(65.6%),少突胶质细胞瘤87例(34.4%)。53例(20.9%)患者术后立即接受辅助治疗,49例(19.3%)患者后续接受AS治疗。平均随访7.1±3.9年,总生存率为80.2%(末次评估时仍存活203例)。1组有更多的患者偶发胶质瘤(p = 0.00009),而2组在手术前有更高的顽固性癫痫发作率(p = 0.0019)和更大的肿瘤体积(p < 0.00001)。尽管如此,两组的EOR和术后难治性癫痫发生率相似,组2恢复工作的患者更多(p = 0.001)。结论:这是迄今为止最大规模的基于清醒定位的经脑包膜切除涉及脑岛的lgg手术经验。结果显示功能保存和恢复工作的比例高,总生存率高。
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来源期刊
Journal of neurosurgery
Journal of neurosurgery 医学-临床神经学
CiteScore
7.20
自引率
7.30%
发文量
1003
审稿时长
1 months
期刊介绍: The Journal of Neurosurgery, Journal of Neurosurgery: Spine, Journal of Neurosurgery: Pediatrics, and Neurosurgical Focus are devoted to the publication of original works relating primarily to neurosurgery, including studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology. The Editors and Editorial Boards encourage submission of clinical and laboratory studies. Other manuscripts accepted for review include technical notes on instruments or equipment that are innovative or useful to clinicians and researchers in the field of neuroscience; papers describing unusual cases; manuscripts on historical persons or events related to neurosurgery; and in Neurosurgical Focus, occasional reviews. Letters to the Editor commenting on articles recently published in the Journal of Neurosurgery, Journal of Neurosurgery: Spine, and Journal of Neurosurgery: Pediatrics are welcome.
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