ORIGINAL RESEARCH article
Front. Oncol.
Sec. Neuro-Oncology and Neurosurgical Oncology
Volume 15 - 2025 | doi: 10.3389/fonc.2025.1703756
Patient Selection and Outcome in Low-Grade Glioma Surgery
Provisionally accepted- 1Department of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden
- 2Karolinska Institutet Institutionen for klinisk neurovetenskap, Stockholm, Sweden
- 3St Olavs Hospital Universitetssykehuset i Trondheim Nevrokirurgisk avdeling, Trondheim, Norway
- 4Sahlgrenska universitetssjukhuset, Gothenburg, Sweden
- 5Goteborgs universitet Sahlgrenska Akademin, Gothenburg, Sweden
- 6Karolinska Universitetssjukhuset, Stockholm, Sweden
- 7St Olav's Hospital HF, Trondheim, Norway
- 8Umea universitet Neurovetenskaper, Umeå, Sweden
- 9Akademiska sjukhuset, Uppsala, Sweden
- 10Haukeland Universitetssjukehus, Bergen, Norway
- 11Universitetssjukhuset i Linkoping, Linköping, Sweden
- 12Skanes universitetssjukhus Lund, Lund, Sweden
- 13Universitetssykehuset Nord-Norge HF, Tromsø, Norway
- 14Norrlands universitetssjukhus, Umeå, Sweden
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Background and Objectives: Maximal safe resection is cornerstone in diffuse low-grade glioma (dLGG) management although epidemiological data are limited. We aim to explore surgical selection, techniques and outcome in a population-based cohort. Materials and methods: Multi-center case series (9 out of 10 neurosurgical departments in Norway and Sweden) of all adults (≥18 years) with histopathologically verified supratentorial dLGG, WHO grade 2, undergoing primary surgery 2012-2017. Complications within 30 days and neurological outcomes at 3 months assessed. Pre-and postoperative MRIs were reviewed centrally, blinded to patient outcome and center. Results: Of 517 included patients, 217 (41.7%) were female, and the mean (SD) age was 44.5 (15.0) years. Biopsy only was performed in 119 (23.0%) patients (13.8-38.9% across centers), and 398 (77.0%) underwent resection (61.1-86.2%). Intraoperative neurophysiological monitoring (IONM) was used in 142 (35.7%, 0-58.7%) resections. The biopsy only patients were older (52.7 years vs. 42.1 years, P<.001), had larger tumors (56.6 ml vs. 31.9 ml, P<.001) more often eloquently located (86.6 % vs. 56.5%, P<.001). The median (IQR) extent of resection (EOR) was 82.9% (63.3-97.7%), 69.7-100.0% across centers. The median (IQR) residual tumor was 4.6 ml (0.5-19.9 ml), 0.0-14.1 ml across centers. Age and histopathology were the most important predictors of EOR. New/worsened neurological deficits occurred in 165 patients (41.5%), 23.1-66.7% across centers, and persisting in 19 (4.8%, 0-22.7%) at 3 months after surgery. A complication was observed in 87 patients (21.4%, 0-31.7%) with 12 patients (3.1%, 0-9.8%) having a grade III-IV complications. Conclusions: We find surgical selection associated with age, tumor size and location. The median EOR in a population-based cohort is 83% with age and tumor biology being significant predictors. EOR did not correlate with higher risks or worse neurological outcome. We provide an epidemiological perspective demonstrating a variation in surgical selection and techniques reflecting persistent controversy in dLGG management.
Keywords: extent of resection, Glioma, low-grade glioma, Neurological deficits, Neurosurgery, oncology, surgical outcomes
Received: 11 Sep 2025; Accepted: 02 Oct 2025.
Copyright: © 2025 Jensdottir, Solheim, Corell, de Dios, Dunås, Fletcher-Sandersjöö, Gulati, Holmgren, Latini, Mahesparan, Milos, Neimantaite, Nittby Redebrandt, Pedersen, Sjöberg, Sjögren, Tomasevic, Tveiten, Gómez Vecchio, Zetterling, Bartek Jr and Jakola. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Margret Jensdottir, margret.jensdottir@ki.se
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