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Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature

INTRODUCTION: Adult brainstem gliomas (BSGs) are rare central nervous system tumours characterized by a highly heterogeneous clinical course. Median survival times range from 11 to 84 months. Beyond surgery, no treatment standard has been established. We investigated clinical and radiological data t...

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Autores principales: Leibetseder, Annette, Leitner, Johannes, Mair, Maximilian J., Meckel, Stephan, Hainfellner, Johannes A., Aichholzer, Martin, Widhalm, Georg, Dieckmann, Karin, Weis, Serge, Furtner, Julia, von Oertzen, Tim, Preusser, Matthias, Pichler, Josef, Berghoff, Anna Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857120/
https://www.ncbi.nlm.nih.gov/pubmed/34342680
http://dx.doi.org/10.1007/s00415-021-10725-0
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author Leibetseder, Annette
Leitner, Johannes
Mair, Maximilian J.
Meckel, Stephan
Hainfellner, Johannes A.
Aichholzer, Martin
Widhalm, Georg
Dieckmann, Karin
Weis, Serge
Furtner, Julia
von Oertzen, Tim
Preusser, Matthias
Pichler, Josef
Berghoff, Anna Sophie
author_facet Leibetseder, Annette
Leitner, Johannes
Mair, Maximilian J.
Meckel, Stephan
Hainfellner, Johannes A.
Aichholzer, Martin
Widhalm, Georg
Dieckmann, Karin
Weis, Serge
Furtner, Julia
von Oertzen, Tim
Preusser, Matthias
Pichler, Josef
Berghoff, Anna Sophie
author_sort Leibetseder, Annette
collection PubMed
description INTRODUCTION: Adult brainstem gliomas (BSGs) are rare central nervous system tumours characterized by a highly heterogeneous clinical course. Median survival times range from 11 to 84 months. Beyond surgery, no treatment standard has been established. We investigated clinical and radiological data to assess prognostic features providing support for treatment decisions. METHODS: 34 BSG patients treated between 2000 and 2019 and aged ≥ 18 years at the time of diagnosis were retrospectively identified from the databases of the two largest Austrian Neuro-Oncology centres. Clinical data including baseline characteristics, clinical disease course, applied therapies, the outcome as well as neuroradiological and neuropathological findings were gathered and analysed. The tumour apparent diffusion coefficient (ADC), volumetry of contrast-enhancing and non-contrast-enhancing lesions were determined on magnetic resonance imaging scans performed at diagnosis. RESULTS: The median age at diagnosis was 38.5 years (range 18–71 years). Tumour progression occurred in 26/34 (76.5%) patients after a median follow up time of 19 months (range 0.9–236.2). Median overall survival (OS) and progression-free survival (PFS) was 24.1 months (range 0.9–236.2; 95% CI 18.1–30.1) and 14.5 months (range 0.7–178.5; 95% CI 5.1–23.9), respectively. Low-performance status, high body mass index (BMI) at diagnosis and WHO grading were associated with shorter PFS and OS at univariate analysis (p < 0.05, log rank test, respectively). ADC values below the median were significantly associated with shorter OS (14.9 vs 44.2 months, p = 0.018). CONCLUSION: ECOG, BMI, WHO grade and ADC values were associated with the survival prognosis of BSG patients and should be included in the prognostic assessment.
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spelling pubmed-88571202022-02-23 Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature Leibetseder, Annette Leitner, Johannes Mair, Maximilian J. Meckel, Stephan Hainfellner, Johannes A. Aichholzer, Martin Widhalm, Georg Dieckmann, Karin Weis, Serge Furtner, Julia von Oertzen, Tim Preusser, Matthias Pichler, Josef Berghoff, Anna Sophie J Neurol Original Communication INTRODUCTION: Adult brainstem gliomas (BSGs) are rare central nervous system tumours characterized by a highly heterogeneous clinical course. Median survival times range from 11 to 84 months. Beyond surgery, no treatment standard has been established. We investigated clinical and radiological data to assess prognostic features providing support for treatment decisions. METHODS: 34 BSG patients treated between 2000 and 2019 and aged ≥ 18 years at the time of diagnosis were retrospectively identified from the databases of the two largest Austrian Neuro-Oncology centres. Clinical data including baseline characteristics, clinical disease course, applied therapies, the outcome as well as neuroradiological and neuropathological findings were gathered and analysed. The tumour apparent diffusion coefficient (ADC), volumetry of contrast-enhancing and non-contrast-enhancing lesions were determined on magnetic resonance imaging scans performed at diagnosis. RESULTS: The median age at diagnosis was 38.5 years (range 18–71 years). Tumour progression occurred in 26/34 (76.5%) patients after a median follow up time of 19 months (range 0.9–236.2). Median overall survival (OS) and progression-free survival (PFS) was 24.1 months (range 0.9–236.2; 95% CI 18.1–30.1) and 14.5 months (range 0.7–178.5; 95% CI 5.1–23.9), respectively. Low-performance status, high body mass index (BMI) at diagnosis and WHO grading were associated with shorter PFS and OS at univariate analysis (p < 0.05, log rank test, respectively). ADC values below the median were significantly associated with shorter OS (14.9 vs 44.2 months, p = 0.018). CONCLUSION: ECOG, BMI, WHO grade and ADC values were associated with the survival prognosis of BSG patients and should be included in the prognostic assessment. Springer Berlin Heidelberg 2021-08-03 2022 /pmc/articles/PMC8857120/ /pubmed/34342680 http://dx.doi.org/10.1007/s00415-021-10725-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Leibetseder, Annette
Leitner, Johannes
Mair, Maximilian J.
Meckel, Stephan
Hainfellner, Johannes A.
Aichholzer, Martin
Widhalm, Georg
Dieckmann, Karin
Weis, Serge
Furtner, Julia
von Oertzen, Tim
Preusser, Matthias
Pichler, Josef
Berghoff, Anna Sophie
Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title_full Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title_fullStr Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title_full_unstemmed Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title_short Prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
title_sort prognostic factors in adult brainstem glioma: a tertiary care center analysis and review of the literature
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857120/
https://www.ncbi.nlm.nih.gov/pubmed/34342680
http://dx.doi.org/10.1007/s00415-021-10725-0
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