Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden

MIB-1 index is an important predictor of meningioma progression and was found to be correlated with COX-2 expression. However, the impact of low-dose acetylsalicylic acid (ASA) on MIB-1 index and clinical symptoms is unclear. Between 2009 and 2022, 710 patients with clinical data, tumor-imaging data...

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Main Authors: Johannes Wach, Ági Güresir, Hartmut Vatter, Ulrich Herrlinger, Albert Becker, Marieta Toma, Michael Hölzel, Erdem Güresir
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/14/17/4285
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author Johannes Wach
Ági Güresir
Hartmut Vatter
Ulrich Herrlinger
Albert Becker
Marieta Toma
Michael Hölzel
Erdem Güresir
author_facet Johannes Wach
Ági Güresir
Hartmut Vatter
Ulrich Herrlinger
Albert Becker
Marieta Toma
Michael Hölzel
Erdem Güresir
author_sort Johannes Wach
collection DOAJ
description MIB-1 index is an important predictor of meningioma progression and was found to be correlated with COX-2 expression. However, the impact of low-dose acetylsalicylic acid (ASA) on MIB-1 index and clinical symptoms is unclear. Between 2009 and 2022, 710 patients with clinical data, tumor-imaging data, inflammatory laboratory (plasma fibrinogen, serum C-reactive protein) data, and neuropathological reports underwent surgery for primary cranial WHO grade 1 and 2 meningioma. ASA intake was found to be significantly associated with a low MIB-1 labeling index in female patients ≥ 60 years. Multivariable analysis demonstrated that female patients ≥ 60 years with a non-skull-base meningioma taking ASA had a significantly lower MIB-1 index (OR: 2.6, 95%: 1.0–6.6, <i>p</i> = 0.04). Furthermore, the intake of ASA was independently associated with a reduced burden of symptomatic epilepsy at presentation in non-skull-base meningiomas in both genders (OR: 3.8, 95%CI: 1.3–10.6, <i>p</i> = 0.03). ASA intake might have an anti-proliferative effect in the subgroup of elderly female patients with non-skull-base meningiomas. Furthermore, anti-inflammatory therapy seems to reduce the burden of symptomatic epilepsy in non-skull-base meningiomas. Further research is needed to investigate the role of anti-inflammatory therapy in non-skull-base meningiomas.
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spelling doaj.art-b433faeadbde4ecc853d68914f8d9dbf2023-11-23T12:52:54ZengMDPI AGCancers2072-66942022-09-011417428510.3390/cancers14174285Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure BurdenJohannes Wach0Ági Güresir1Hartmut Vatter2Ulrich Herrlinger3Albert Becker4Marieta Toma5Michael Hölzel6Erdem Güresir7Department of Neurosurgery, University Hospital Bonn, 53127 Bonn, GermanyDepartment of Neurosurgery, University Hospital Bonn, 53127 Bonn, GermanyDepartment of Neurosurgery, University Hospital Bonn, 53127 Bonn, GermanyDivision of Clinical Neurooncology, Department of Neurology and Centre of Integrated Oncology, University Hospital Bonn, 53127 Bonn, GermanyDepartment of Neuropathology, University Hospital Bonn, 53127 Bonn, GermanyInstitute of Pathology, University Hospital Bonn, 53127 Bonn, GermanyInstitute of Experimental Oncology, University Hospital Bonn, 53127 Bonn, GermanyDepartment of Neurosurgery, University Hospital Bonn, 53127 Bonn, GermanyMIB-1 index is an important predictor of meningioma progression and was found to be correlated with COX-2 expression. However, the impact of low-dose acetylsalicylic acid (ASA) on MIB-1 index and clinical symptoms is unclear. Between 2009 and 2022, 710 patients with clinical data, tumor-imaging data, inflammatory laboratory (plasma fibrinogen, serum C-reactive protein) data, and neuropathological reports underwent surgery for primary cranial WHO grade 1 and 2 meningioma. ASA intake was found to be significantly associated with a low MIB-1 labeling index in female patients ≥ 60 years. Multivariable analysis demonstrated that female patients ≥ 60 years with a non-skull-base meningioma taking ASA had a significantly lower MIB-1 index (OR: 2.6, 95%: 1.0–6.6, <i>p</i> = 0.04). Furthermore, the intake of ASA was independently associated with a reduced burden of symptomatic epilepsy at presentation in non-skull-base meningiomas in both genders (OR: 3.8, 95%CI: 1.3–10.6, <i>p</i> = 0.03). ASA intake might have an anti-proliferative effect in the subgroup of elderly female patients with non-skull-base meningiomas. Furthermore, anti-inflammatory therapy seems to reduce the burden of symptomatic epilepsy in non-skull-base meningiomas. Further research is needed to investigate the role of anti-inflammatory therapy in non-skull-base meningiomas.https://www.mdpi.com/2072-6694/14/17/4285acetylsalicylic acidaspirinmeningiomaproliferationseizure
spellingShingle Johannes Wach
Ági Güresir
Hartmut Vatter
Ulrich Herrlinger
Albert Becker
Marieta Toma
Michael Hölzel
Erdem Güresir
Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
Cancers
acetylsalicylic acid
aspirin
meningioma
proliferation
seizure
title Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
title_full Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
title_fullStr Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
title_full_unstemmed Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
title_short Low-Dose Acetylsalicylic Acid Treatment in Non-Skull-Base Meningiomas: Impact on Tumor Proliferation and Seizure Burden
title_sort low dose acetylsalicylic acid treatment in non skull base meningiomas impact on tumor proliferation and seizure burden
topic acetylsalicylic acid
aspirin
meningioma
proliferation
seizure
url https://www.mdpi.com/2072-6694/14/17/4285
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