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Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience

INTRODUCTION: Glioblastoma is the most common malignant brain tumour in adults. Among all gliomas, it is the most aggressive type, with a high fatality rate, and according to the WHO classification, it is a grade IV tumour. As this tumour is well-known for its poor survival, an understanding of clin...

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Autores principales: Jilla, Swapna, Prathipati, Archana, Subramanian, Bala Venkata, Das, Pranabandhu, Valiyaveettil, Deepthi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300392/
https://www.ncbi.nlm.nih.gov/pubmed/35919238
http://dx.doi.org/10.3332/ecancer.2022.1386
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author Jilla, Swapna
Prathipati, Archana
Subramanian, Bala Venkata
Das, Pranabandhu
Valiyaveettil, Deepthi
author_facet Jilla, Swapna
Prathipati, Archana
Subramanian, Bala Venkata
Das, Pranabandhu
Valiyaveettil, Deepthi
author_sort Jilla, Swapna
collection PubMed
description INTRODUCTION: Glioblastoma is the most common malignant brain tumour in adults. Among all gliomas, it is the most aggressive type, with a high fatality rate, and according to the WHO classification, it is a grade IV tumour. As this tumour is well-known for its poor survival, an understanding of clinical and treatment-related prognostic factors can help in tailored treatment. The aim of this study was to know the impact of prognostic factors on survival in these cases. MATERIALS AND METHODS: All glioblastoma patients treated in our hospital during 2010–2015 were included in the analysis. Cases were divided into different groups based on prognostic factors. Overall survival (OS) and disease-free survival (DFS) were calculated and compared among the different groups. Statistical analysis was carried out using SPSS software v20. RESULTS: One-year OS was 36.9% and 2-year OS was 10.8%. One-year DFS was 13.04%. On univariate analysis, age at presentation ≤45 years and adjuvant chemotherapy with six cycles or more temozolomide improved OS and DFS. Multivariate analysis retained the statistically significant positive impact of usage of adjuvant temozolomide chemotherapy of ≥six cycles on OS and DFS. The use of the anti-epileptic drug Levetiracetam had a statistically significant improvement of DFS. CONCLUSION: Among various clinical and treatment-related prognostic factors evaluated in our study, younger age at presentation and addition of temozolomide chemotherapy to radiation showed improvement in OS and DFS. The use of the anti-epileptic drug Levetiracetam had an impact on DFS in glioblastoma patients.
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spelling pubmed-93003922022-08-01 Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience Jilla, Swapna Prathipati, Archana Subramanian, Bala Venkata Das, Pranabandhu Valiyaveettil, Deepthi Ecancermedicalscience Research INTRODUCTION: Glioblastoma is the most common malignant brain tumour in adults. Among all gliomas, it is the most aggressive type, with a high fatality rate, and according to the WHO classification, it is a grade IV tumour. As this tumour is well-known for its poor survival, an understanding of clinical and treatment-related prognostic factors can help in tailored treatment. The aim of this study was to know the impact of prognostic factors on survival in these cases. MATERIALS AND METHODS: All glioblastoma patients treated in our hospital during 2010–2015 were included in the analysis. Cases were divided into different groups based on prognostic factors. Overall survival (OS) and disease-free survival (DFS) were calculated and compared among the different groups. Statistical analysis was carried out using SPSS software v20. RESULTS: One-year OS was 36.9% and 2-year OS was 10.8%. One-year DFS was 13.04%. On univariate analysis, age at presentation ≤45 years and adjuvant chemotherapy with six cycles or more temozolomide improved OS and DFS. Multivariate analysis retained the statistically significant positive impact of usage of adjuvant temozolomide chemotherapy of ≥six cycles on OS and DFS. The use of the anti-epileptic drug Levetiracetam had a statistically significant improvement of DFS. CONCLUSION: Among various clinical and treatment-related prognostic factors evaluated in our study, younger age at presentation and addition of temozolomide chemotherapy to radiation showed improvement in OS and DFS. The use of the anti-epileptic drug Levetiracetam had an impact on DFS in glioblastoma patients. Cancer Intelligence 2022-05-12 /pmc/articles/PMC9300392/ /pubmed/35919238 http://dx.doi.org/10.3332/ecancer.2022.1386 Text en © the authors; licensee ecancermedicalscience. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Jilla, Swapna
Prathipati, Archana
Subramanian, Bala Venkata
Das, Pranabandhu
Valiyaveettil, Deepthi
Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title_full Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title_fullStr Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title_full_unstemmed Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title_short Impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
title_sort impact of various prognostic factors on survival in glioblastoma: tertiary care institutional experience
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300392/
https://www.ncbi.nlm.nih.gov/pubmed/35919238
http://dx.doi.org/10.3332/ecancer.2022.1386
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