This work is licensed under the Creative Commons Attribution 4.0 International License.
Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A, et al. The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol 2007;114: 97–109. doi: 10.1007/s00401-007-0243-4LouisDNOhgakiHWiestlerODCaveneeWKBurgerPCJouvetAThe 2007 WHO classification of tumours of the central nervous system20071149710910.1007/s00401-007-0243-4Open DOISearch in Google Scholar
Smrdel U, Popovic M, Zwitter M, Bostjancic E, Zupan A, Kovac V, et al. Long-term survival in glioblastoma: methyl guanine methyl transferase (MGMT) promoter methylation as independent favourable prognostic factor. Radiol Oncol 2015; 50: 394–401. doi: 10.1515/raon-2015-0041SmrdelUPopovicMZwitterMBostjancicEZupanAKovacVLong-term survival in glioblastoma: methyl guanine methyl transferase (MGMT) promoter methylation as independent favourable prognostic factor20155039440110.1515/raon-2015-0041Open DOISearch in Google Scholar
Millward CP, Brodbelt AR, Haylock B, Zakaria R, Baborie A, Crooks D, et al. The impact of MGMT methylation and IDH-1 mutation on long-term outcome for glioblastoma treated with chemoradiotherapy. Acta Neurochir 2016; 158: 1943–53. doi: 10.1007/s00701-016-2928-8MillwardCPBrodbeltARHaylockBZakariaRBaborieACrooksDThe impact of MGMT methylation and IDH-1 mutation on long-term outcome for glioblastoma treated with chemoradiotherapy201615819435310.1007/s00701-016-2928-8Open DOISearch in Google Scholar
Kurdi M, Shafique Butt N, Baeesa S, Alghamdi B, Maghrabi Y, Bardeesi A, et al. The impact of IDH1 mutation and MGMT promoter methylation on recurrence-free interval in glioblastoma patients treated with radiotherapy and chemotherapeutic agents. Pathol Oncol Res 2021; 27: 1609778. doi: 10.3389/pore.2021.1609778KurdiMShafique ButtNBaeesaSAlghamdiBMaghrabiYBardeesiAThe impact of IDH1 mutation and MGMT promoter methylation on recurrence-free interval in glioblastoma patients treated with radiotherapy and chemotherapeutic agents202127160977810.3389/pore.2021.1609778Open DOISearch in Google Scholar
Sinha R, Stephenson JM, Price SJ. A systematic review of cognitive function in patients with glioblastoma undergoing surgery. Neuro-oncology Pract 2020; 7: 131–42. doi: 10.1093/nop/npz018SinhaRStephensonJMPriceSJA systematic review of cognitive function in patients with glioblastoma undergoing surgery202071314210.1093/nop/npz018Open DOISearch in Google Scholar
Van Kessel E, Emons MAC, Wajer IH, Van Baarsen KM, Broekman ML, Robe PA, et al. Tumor-related neurocognitive dysfunction in patients with diffuse glioma: a retrospective cohort study prior to antitumor treatment. Neuro-Oncology Pract 2019; 6: 463. doi: 10.1093/nop/npz008Van KesselEEmonsMACWajerIHVan BaarsenKMBroekmanMLRobePATumor-related neurocognitive dysfunction in patients with diffuse glioma: a retrospective cohort study prior to antitumor treatment2019646310.1093/nop/npz008Open DOISearch in Google Scholar
Taphoorn MJB, Klein M. Cognitive deficits in adult patients with brain tumours. Lancet Neurology 2004; 3: 159–68. doi: 10.1016/S1474-4422(04)00680-5TaphoornMJBKleinMCognitive deficits in adult patients with brain tumours200431596810.1016/S1474-4422(04)00680-5Open DOISearch in Google Scholar
Jütten K, Mainz V, Gauggel S, Patel HJ, Binkofski F, Wiesmann M, et al. Diffusion tensor imaging reveals microstructural heterogeneity of normal-appearing white matter and related cognitive dysfunction in glioma patients. Front Oncol 2019; 9: 536. doi: 10.3389/fonc.2019.00536JüttenKMainzVGauggelSPatelHJBinkofskiFWiesmannMDiffusion tensor imaging reveals microstructural heterogeneity of normal-appearing white matter and related cognitive dysfunction in glioma patients2019953610.3389/fonc.2019.00536Open DOISearch in Google Scholar
Van Kessel E, Snijders TJ, Anniek ·, Baumfalk E, Ruis C, Van Baarsen KM, et al. Neurocognitive changes after awake surgery in glioma patients: a retrospective cohort study. J Neurooncol 2020; 146: 97–109. doi: 10.1007/s11060-019-03341-6Van KesselESnijdersTJBaumfalkAnniek ERuisCVan BaarsenKMNeurocognitive changes after awake surgery in glioma patients: a retrospective cohort study20201469710910.1007/s11060-019-03341-6Open DOISearch in Google Scholar
Meyers CA, Hess KR. Neuro-oncology multifaceted end points in brain tumor clinical trials: cognitive deterioration precedes MRI progression. Neuro-Oncology2003; 5: 89–95. doi: 10.1093/neuonc/5.2.89MeyersCAHessKRNeuro-oncology multifaceted end points in brain tumor clinical trials: cognitive deterioration precedes MRI progression20035899510.1093/neuonc/5.2.89Open DOISearch in Google Scholar
Armstrong CL, Goldstein B, Shera D, Ledakis GE, Tallent EM. The predictive value of longitudinal neuropsychologic assessment in the early detection of brain tumor recurrence. Cancer 2003; 97: 649–56. doi: 10.1002/cncr.11099ArmstrongCLGoldsteinBSheraDLedakisGETallentEMThe predictive value of longitudinal neuropsychologic assessment in the early detection of brain tumor recurrence2003976495610.1002/cncr.11099Open DOISearch in Google Scholar
Flechl B, Sax C, Ackerl M, Crevenna R, Woehrer A, Hainfellner J, et al. The course of quality of life and neurocognition in newly diagnosed patients with glioblastoma. Radiother Oncol 2017; 125: 228–33. doi: 10.1016/j.radonc.2017.07.027FlechlBSaxCAckerlMCrevennaRWoehrerAHainfellnerJThe course of quality of life and neurocognition in newly diagnosed patients with glioblastoma20171252283310.1016/j.radonc.2017.07.027Open DOISearch in Google Scholar
Johnson DR, Sawyer AM, Meyers CA, Patrick B, Neill O’, Wefel JS. Early measures of cognitive function predict survival in patients with newly diagnosed glioblastoma. Neuro Oncol 2012; 14: 808–16. doi: 10.1093/neuonc/nos082JohnsonDRSawyerAMMeyersCAO’NeillPatrick BWefelJSEarly measures of cognitive function predict survival in patients with newly diagnosed glioblastoma2012148081610.1093/neuonc/nos082Open DOISearch in Google Scholar
Meyers CA, Hess KR, Yung WKA, Levin VA. Cognitive function as a predictor of survival in patients with recurrent malignant glioma. J Clin Oncol 2000; 18: 646–50. doi: 10.1200/JCO.2000.18.3.646MeyersCAHessKRYungWKALevinVACognitive function as a predictor of survival in patients with recurrent malignant glioma2000186465010.1200/JCO.2000.18.3.646Open DOISearch in Google Scholar
Lee ST, Park CK, Kim JW, Park MJ, Lee H, Lim JA, et al. Early cognitive function tests predict early progression in glioblastoma. Neuro-oncology Pract 2015; 2: 137–43. doi: 10.1093/nop/npv007LeeSTParkCKKimJWParkMJLeeHLimJAEarly cognitive function tests predict early progression in glioblastoma201521374310.1093/nop/npv007Open DOISearch in Google Scholar
Butterbrod E, Synhaeve N, Rutten GJ, Schwabe I, Gehring K, Sitskoorn M. Cognitive impairment three months after surgery is an independent predictor of survival time in glioblastoma patients. J Neurooncol 2020; 149: 103–11. doi: 10.1007/s11060-020-03577-7ButterbrodESynhaeveNRuttenGJSchwabeIGehringKSitskoornMCognitive impairment three months after surgery is an independent predictor of survival time in glioblastoma patients20201491031110.1007/s11060-020-03577-7Open DOISearch in Google Scholar
Derks J, Kulik S, Wesseling P, Numan T, Hillebrand A, van Dellen E, et al. Understanding cognitive functioning in glioma patients: the relevance of IDH-mutation status and functional connectivity. Brain Behav 2019; 9: e01204.doi: 10.1002/brb3.1204DerksJKulikSWesselingPNumanTHillebrandAvan DellenEUnderstanding cognitive functioning in glioma patients: the relevance of IDH-mutation status and functional connectivity20199e0120410.1002/brb3.1204Open DOISearch in Google Scholar
van Kessel E, Snijders TJ, Baumfalk AE, Ruis C, van Baarsen KM, Broekman ML, et al. Neurocognitive changes after awake surgery in glioma patients: a retrospective cohort study. J Neurooncol 2020; 146: 97–109. doi: 10.1007/s11060-019-03341-6van KesselESnijdersTJBaumfalkAERuisCvan BaarsenKMBroekmanMLNeurocognitive changes after awake surgery in glioma patients: a retrospective cohort study20201469710910.1007/s11060-019-03341-6Open DOISearch in Google Scholar
Wefel JS, Noll KR, Rao G, Cahill DP. Neurocognitive function varies by IDH1 genetic mutation status in patients with malignant glioma prior to surgical resection. Neuro Oncol 2016; 18: 1656–63. doi: 10.1093/neuonc/now165WefelJSNollKRRaoGCahillDPNeurocognitive function varies by IDH1 genetic mutation status in patients with malignant glioma prior to surgical resection20161816566310.1093/neuonc/now165Open DOISearch in Google Scholar
Bunevicius A, Miller J, Parsons M. Isocitrate dehydrogenase, patient-reported outcomes, and cognitive functioning of glioma patients: a systematic review. Curr Oncol Rep 2020; 22: 120. doi: 10.1007/s11912-020-00978-9BuneviciusAMillerJParsonsMIsocitrate dehydrogenase, patient-reported outcomes, and cognitive functioning of glioma patients: a systematic review20202212010.1007/s11912-020-00978-9Open DOISearch in Google Scholar
Weller J, Tzaridis T, Mack F, Steinbach JP, Schlegel U, Hau P, et al. Health-related quality of life and neurocognitive functioning with lomustine-temozolomide versus temozolomide in patients with newly diagnosed, MGMT-methylated glioblastoma (CeTeG/NOA-09): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol 2019; 20: 1444–53. doi: 10.1016/S1470-2045(19)30502-9WellerJTzaridisTMackFSteinbachJPSchlegelUHauPHealth-related quality of life and neurocognitive functioning with lomustine-temozolomide versus temozolomide in patients with newly diagnosed, MGMT-methylated glioblastoma (CeTeG/NOA-09): a randomised, multicentre, open-label, phase 3 trial20192014445310.1016/S1470-2045(19)30502-9Open DOISearch in Google Scholar
Wang Q, Xiao F, Qi F, Song X, Yu Y. Risk factors for cognitive impairment in high-grade glioma patients treated with postoperative radiochemotherapy. Cancer Res Treat 2020; 52: 586–93. doi: 10.4143/crt.2019.242WangQXiaoFQiFSongXYuYRisk factors for cognitive impairment in high-grade glioma patients treated with postoperative radiochemotherapy2020525869310.4143/crt.2019.242Open DOISearch in Google Scholar
Herzog A. [Validity and reliability of the new Slovenian Test of Word Learning]. [Slovenian]. [graduation thesis]. Ljubljana: Universty of Ljubljana; 2015.HerzogALjubljanaUniversty of Ljubljana2015Search in Google Scholar
Remšak T. [Development of the Spelling Fluency Test]. [Slovenian]. [graduation thesis]. Ljubljana: Universty of Ljubljana; 2013.RemšakTLjubljanaUniversty of Ljubljana2013Search in Google Scholar
Sánchez-Cubillo I, Periáñez JA, Adrover-Roig D, Rodríguez-Sánchez JM, Ríos-Lago M, Tirapu J, et al. Construct validity of the Trail Making Test: role of task-switching, working memory, inhibition/interference control, and visuomotor abilities. J Int Neuropsychol Soc 2009; 15: 438–50. doi: 10.1017/S1355617709090626Sánchez-CubilloIPeriáñezJAAdrover-RoigDRodríguez-SánchezJMRíos-LagoMTirapuJConstruct validity of the Trail Making Test: role of task-switching, working memory, inhibition/interference control, and visuomotor abilities2009154385010.1017/S1355617709090626Open DOISearch in Google Scholar
Wefel JS, Vardy J, Ahles T, Schagen SB. International Cognition and Cancer Task Force recommendations to harmonise studies of cognitive function in patients with cancer. Lancet Oncol 2011; 12: 703–8. doi: 10.1016/S1470-2045(10)70294-1WefelJSVardyJAhlesTSchagenSBInternational Cognition and Cancer Task Force recommendations to harmonise studies of cognitive function in patients with cancer201112703810.1016/S1470-2045(10)70294-1Open DOISearch in Google Scholar
Iorgulescu JB, Sun C, Neff C, Cioffi G, Gutierrez C, Kruchko C, et al. Molecular biomarker-defined brain tumors: epidemiology, validity, and completeness in the United States. Neuro Oncol 2022; 24: 1989–2000. doi: 10.1093/neuonc/noac113IorgulescuJBSunCNeffCCioffiGGutierrezCKruchkoCMolecular biomarker-defined brain tumors: epidemiology, validity, and completeness in the United States2022241989200010.1093/neuonc/noac113Open DOISearch in Google Scholar
Capper D, Mittelbronn M, Meyermann R, Schittenhelm J. Pitfalls in the assessment of MGMT expression and in its correlation with survival in diffuse astrocytomas: proposal of a feasible immunohistochemical approach. Acta Neuropathol 2008; 115: 249–59. doi: 10.1007/s00401-007-0310-xCapperDMittelbronnMMeyermannRSchittenhelmJPitfalls in the assessment of MGMT expression and in its correlation with survival in diffuse astrocytomas: proposal of a feasible immunohistochemical approach20081152495910.1007/s00401-007-0310-xOpen DOISearch in Google Scholar
Tucha O, Smely C, Preier M, Lange KW. Cognitive deficits before treatment among patients with brain tumors. Neurosurgery 2000; 47: 324–33. doi: 10.1097/00006123-200008000-00011TuchaOSmelyCPreierMLangeKWCognitive deficits before treatment among patients with brain tumors2000473243310.1097/00006123-200008000-00011Open DOISearch in Google Scholar
Kesler SR, Noll K, Cahill DP, Rao G, Wefel JS. The effect of IDH1 mutation on the structural connectome in malignant astrocytoma. J Neurooncol 2017; 131: 565–74. doi: 10.1007/s11060-016-2328-1KeslerSRNollKCahillDPRaoGWefelJSThe effect of IDH1 mutation on the structural connectome in malignant astrocytoma20171315657410.1007/s11060-016-2328-1Open DOISearch in Google Scholar
Van Kessel E, Snijders TJ, Anniek·, Baumfalk E, Ruis C, Van Baarsen KM, et al. Neurocognitive changes after awake surgery in glioma patients: a retrospective cohort study. J Neurooncol 2020; 146: 97–109. doi: 10.1007/s11060-019-03341-6Van KesselESnijdersTJBaumfalkAnniek ERuisCVan BaarsenKMNeurocognitive changes after awake surgery in glioma patients: a retrospective cohort study20201469710910.1007/s11060-019-03341-6Open DOISearch in Google Scholar