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Survival Outcomes and Prognostic Factors in Glioblastoma

SIMPLE SUMMARY: Glioblastoma is the most common tumour that originates in the brain in adults. Most of the published data on glioblastoma are from patients in clinical trials who tend to be younger and fitter than the average patient. We therefore looked at patient demographic, tumour characteristic...

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Autores principales: Brown, Nicholas F., Ottaviani, Diego, Tazare, John, Gregson, John, Kitchen, Neil, Brandner, Sebastian, Fersht, Naomi, Mulholland, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265012/
https://www.ncbi.nlm.nih.gov/pubmed/35804940
http://dx.doi.org/10.3390/cancers14133161
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author Brown, Nicholas F.
Ottaviani, Diego
Tazare, John
Gregson, John
Kitchen, Neil
Brandner, Sebastian
Fersht, Naomi
Mulholland, Paul
author_facet Brown, Nicholas F.
Ottaviani, Diego
Tazare, John
Gregson, John
Kitchen, Neil
Brandner, Sebastian
Fersht, Naomi
Mulholland, Paul
author_sort Brown, Nicholas F.
collection PubMed
description SIMPLE SUMMARY: Glioblastoma is the most common tumour that originates in the brain in adults. Most of the published data on glioblastoma are from patients in clinical trials who tend to be younger and fitter than the average patient. We therefore looked at patient demographic, tumour characteristics, and treatments received in a group of 490 real-world patients with glioblastoma to evaluate their survival, and to investigate whether we could find any factors that were associated with longer survival. Overall, the average survival of patients was 9 months. Patients tended to live longer if they were younger, had surgery, if they had further treatment after surgery (chemo- or radio-therapy), or if they had a tumour marker called MGMT promotor methylation. ABSTRACT: Background: IDH-wildtype glioblastoma is the most common malignant primary brain tumour in adults. As there is limited information on prognostic factors outside of clinical trials; thus, we conducted a retrospective study to characterise the glioblastoma population at our centre. Methods: Demographic, tumour molecular profiles, treatment, and survival data were collated for patients diagnosed with glioblastoma at our centre between July 2011 and December 2015. We used multivariate proportional hazard model associations with survival. Results: 490 patients were included; 60% had debulking surgery and 40% biopsy only. Subsequently, 56% had standard chemoradiotherapy, 25% had non-standard chemo/radio-therapy, and 19% had no further treatment. Overall survival was 9.2 months. In the multivariate analysis, longer survival was associated with debulking surgery vs. biopsy alone (14.9 vs. 8 months) (HR 0.54 [95% CI 0.41–0.70]), subsequent treatment after diagnosis (HR 0.12 [0.08–0.16]) (standard chemoradiotherapy [16.9 months] vs. non-standard regimens [9.2 months] vs. none [2.0 months]), tumour MGMT promotor methylation (HR 0.71 [0.58–0.87]), and younger age (hazard ratio vs. age < 50: 1.70 [1.26–2.30] for ages 50–59; 3.53 [2.65–4.70] for ages 60–69; 4.82 [3.54–6.56] for ages 70+). Conclusions: The median survival for patients with glioblastoma is less than a year. Younger age, debulking surgery, treatment with chemoradiotherapy, and MGMT promotor methylation are independently associated with longer survival.
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spelling pubmed-92650122022-07-09 Survival Outcomes and Prognostic Factors in Glioblastoma Brown, Nicholas F. Ottaviani, Diego Tazare, John Gregson, John Kitchen, Neil Brandner, Sebastian Fersht, Naomi Mulholland, Paul Cancers (Basel) Article SIMPLE SUMMARY: Glioblastoma is the most common tumour that originates in the brain in adults. Most of the published data on glioblastoma are from patients in clinical trials who tend to be younger and fitter than the average patient. We therefore looked at patient demographic, tumour characteristics, and treatments received in a group of 490 real-world patients with glioblastoma to evaluate their survival, and to investigate whether we could find any factors that were associated with longer survival. Overall, the average survival of patients was 9 months. Patients tended to live longer if they were younger, had surgery, if they had further treatment after surgery (chemo- or radio-therapy), or if they had a tumour marker called MGMT promotor methylation. ABSTRACT: Background: IDH-wildtype glioblastoma is the most common malignant primary brain tumour in adults. As there is limited information on prognostic factors outside of clinical trials; thus, we conducted a retrospective study to characterise the glioblastoma population at our centre. Methods: Demographic, tumour molecular profiles, treatment, and survival data were collated for patients diagnosed with glioblastoma at our centre between July 2011 and December 2015. We used multivariate proportional hazard model associations with survival. Results: 490 patients were included; 60% had debulking surgery and 40% biopsy only. Subsequently, 56% had standard chemoradiotherapy, 25% had non-standard chemo/radio-therapy, and 19% had no further treatment. Overall survival was 9.2 months. In the multivariate analysis, longer survival was associated with debulking surgery vs. biopsy alone (14.9 vs. 8 months) (HR 0.54 [95% CI 0.41–0.70]), subsequent treatment after diagnosis (HR 0.12 [0.08–0.16]) (standard chemoradiotherapy [16.9 months] vs. non-standard regimens [9.2 months] vs. none [2.0 months]), tumour MGMT promotor methylation (HR 0.71 [0.58–0.87]), and younger age (hazard ratio vs. age < 50: 1.70 [1.26–2.30] for ages 50–59; 3.53 [2.65–4.70] for ages 60–69; 4.82 [3.54–6.56] for ages 70+). Conclusions: The median survival for patients with glioblastoma is less than a year. Younger age, debulking surgery, treatment with chemoradiotherapy, and MGMT promotor methylation are independently associated with longer survival. MDPI 2022-06-28 /pmc/articles/PMC9265012/ /pubmed/35804940 http://dx.doi.org/10.3390/cancers14133161 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brown, Nicholas F.
Ottaviani, Diego
Tazare, John
Gregson, John
Kitchen, Neil
Brandner, Sebastian
Fersht, Naomi
Mulholland, Paul
Survival Outcomes and Prognostic Factors in Glioblastoma
title Survival Outcomes and Prognostic Factors in Glioblastoma
title_full Survival Outcomes and Prognostic Factors in Glioblastoma
title_fullStr Survival Outcomes and Prognostic Factors in Glioblastoma
title_full_unstemmed Survival Outcomes and Prognostic Factors in Glioblastoma
title_short Survival Outcomes and Prognostic Factors in Glioblastoma
title_sort survival outcomes and prognostic factors in glioblastoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265012/
https://www.ncbi.nlm.nih.gov/pubmed/35804940
http://dx.doi.org/10.3390/cancers14133161
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