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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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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. |
format | Online Article Text |
id | pubmed-8857120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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