Preoperative and early postoperative seizures in patients with glioblastoma—two sides of the same coin?

Author:

Ahmadipour Yahya12,Rauschenbach Laurèl123,Santos Alejandro1,Darkwah Oppong Marvin12ORCID,Lazaridis Lazaros245,Quesada Carlos M5,Junker Andreas6,Pierscianek Daniela12,Dammann Philipp12,Wrede Karsten H12,Scheffler Björn23,Glas Martin245,Stuschke Martin27,Sure Ulrich12,Jabbarli Ramazan12ORCID

Affiliation:

1. Department of Neurosurgery and Spine Surgery, University Hospital Essen, Essen, Germany

2. German Cancer Consortium, Partner Site University Hospital Essen, Essen, Germany

3. DKFZ-Division Translational Neurooncology at the WTZ, German Cancer Research Center (DKFZ) Heidelberg and German Cancer Consortium (DKTK) Partner Site University Hospital Essen, Essen, Germany

4. Division of Clinical Neurooncology, Department of Neurology, University Hospital Essen, Essen, Germany

5. Department for Neurology, University Hospital Essen, Essen, Germany

6. Department of Neuropathology, University Hospital Essen, Essen, Germany

7. Department of Radiotherapy, University Hospital Essen, Essen, Germany

Abstract

Abstract Background Symptomatic epilepsy is a common symptom of glioblastoma, which may occur in different stages of disease. There are discrepant reports on association between early seizures and glioblastoma survival, even less is known about the background of these seizures. We aimed at analyzing the risk factors and clinical impact of perioperative seizures in glioblastoma. Methods All consecutive cases with de-novo glioblastoma treated at our institution between 01/2006 and 12/2018 were eligible for this study. Perioperative seizures were stratified into seizures at onset (SAO) and early postoperative seizures (EPS, ≤21days after surgery). Associations between patients characteristics and overall survival (OS) with SAO and EPS were addressed. Results In the final cohort (n = 867), SAO and EPS occurred in 236 (27.2%) and 67 (7.7%) patients, respectively. SAO were independently predicted by younger age (P = .009), higher KPS score (P = .002), tumor location (parietal lobe, P = .001), GFAP expression (≥35%, P = .045), and serum chloride at admission (>102 mmol/L, P = .004). In turn, EPS were independently associated with tumor location (frontal or temporal lobe, P = .013) and pathologic laboratory values at admission (hemoglobin < 12 g/dL, [P = .044], CRP > 1.0 mg/dL [P = 0.036], and GGT > 55 U/L [P = 0.025]). Finally, SAO were associated with gross-total resection (P = .006) and longer OS (P = .030), whereas EPS were related to incomplete resection (P = .005) and poorer OS (P = .009). Conclusions In glioblastoma patients, SAO and EPS seem to have quite different triggers and contrary impact on treatment success and OS. The clinical characteristics of SAO and EPS patients might contribute to the observed survival differences.

Funder

University of Duisburg-Essen

Publisher

Oxford University Press (OUP)

Subject

Electrical and Electronic Engineering,Building and Construction

Reference50 articles.

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