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A Retrospective Study on Spinal Dissemination of Supratentorial Glioma
OBJECTIVE: Metastatic spinal dissemination (MSD) of supratentorial glioma is very rare and there is no established standard of care. The current study investigates the clinical characteristics and course of spinal dissemination of supratentorial glioma. METHODS: A retrospective analysis of adult pat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727749/ https://www.ncbi.nlm.nih.gov/pubmed/35004286 http://dx.doi.org/10.3389/fonc.2021.765399 |
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author | Chen, Jianxin Yang, Fan Shi, Qi Zhao, Yuze Huang, Hongyan |
author_facet | Chen, Jianxin Yang, Fan Shi, Qi Zhao, Yuze Huang, Hongyan |
author_sort | Chen, Jianxin |
collection | PubMed |
description | OBJECTIVE: Metastatic spinal dissemination (MSD) of supratentorial glioma is very rare and there is no established standard of care. The current study investigates the clinical characteristics and course of spinal dissemination of supratentorial glioma. METHODS: A retrospective analysis of adult patients with MSD of supratentorial glioma treated in the Department of Oncology in Beijing Shijitan Hospital, Capital Medical University from June 2012 until August 2021 was performed. The time to event was estimated using Kaplan–Meier analysis. Univariate analyses were performed using log-rank test and multivariate analysis was performed using the Cox proportional hazards model. RESULTS: Thirty-four adult patients with MSD of supratentorial glioma were enrolled in this retrospective study. The median time to MSD (TTMSD) and overall survival (OS) were 5 months (range: 0–78 months) and 15 months (range: 0.7–85 months), respectively, in the entire cohort. Univariate analysis demonstrated that the patients who had received TMZ therapy had a longer TTMSD than those who did not (mTTMSD: 15 vs. 3 months, log-rank P = 0.0004). Furthermore, a protracted duration of salvage chemotherapy of >6 months after MSD was associated with longer OS of the patients with MSD of supratentorial glioma (mOS: 13 vs. 5 months, log-rank P = 0.0163) and reduced the death risk by 64.3% (hazard ratio: 0.357, 95% CI: 0.141–0.901, P = 0.029) compared with a duration ≤6 months. CONCLUSION: Patients with MSD of supratentorial glioma experienced poor prognosis and adjuvant chemotherapy may delay the occurrence of MSD. The protracted duration of systemic salvage chemotherapy may favor survival after spinal dissemination. |
format | Online Article Text |
id | pubmed-8727749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87277492022-01-06 A Retrospective Study on Spinal Dissemination of Supratentorial Glioma Chen, Jianxin Yang, Fan Shi, Qi Zhao, Yuze Huang, Hongyan Front Oncol Oncology OBJECTIVE: Metastatic spinal dissemination (MSD) of supratentorial glioma is very rare and there is no established standard of care. The current study investigates the clinical characteristics and course of spinal dissemination of supratentorial glioma. METHODS: A retrospective analysis of adult patients with MSD of supratentorial glioma treated in the Department of Oncology in Beijing Shijitan Hospital, Capital Medical University from June 2012 until August 2021 was performed. The time to event was estimated using Kaplan–Meier analysis. Univariate analyses were performed using log-rank test and multivariate analysis was performed using the Cox proportional hazards model. RESULTS: Thirty-four adult patients with MSD of supratentorial glioma were enrolled in this retrospective study. The median time to MSD (TTMSD) and overall survival (OS) were 5 months (range: 0–78 months) and 15 months (range: 0.7–85 months), respectively, in the entire cohort. Univariate analysis demonstrated that the patients who had received TMZ therapy had a longer TTMSD than those who did not (mTTMSD: 15 vs. 3 months, log-rank P = 0.0004). Furthermore, a protracted duration of salvage chemotherapy of >6 months after MSD was associated with longer OS of the patients with MSD of supratentorial glioma (mOS: 13 vs. 5 months, log-rank P = 0.0163) and reduced the death risk by 64.3% (hazard ratio: 0.357, 95% CI: 0.141–0.901, P = 0.029) compared with a duration ≤6 months. CONCLUSION: Patients with MSD of supratentorial glioma experienced poor prognosis and adjuvant chemotherapy may delay the occurrence of MSD. The protracted duration of systemic salvage chemotherapy may favor survival after spinal dissemination. Frontiers Media S.A. 2021-12-22 /pmc/articles/PMC8727749/ /pubmed/35004286 http://dx.doi.org/10.3389/fonc.2021.765399 Text en Copyright © 2021 Chen, Yang, Shi, Zhao and Huang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Chen, Jianxin Yang, Fan Shi, Qi Zhao, Yuze Huang, Hongyan A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title | A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title_full | A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title_fullStr | A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title_full_unstemmed | A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title_short | A Retrospective Study on Spinal Dissemination of Supratentorial Glioma |
title_sort | retrospective study on spinal dissemination of supratentorial glioma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727749/ https://www.ncbi.nlm.nih.gov/pubmed/35004286 http://dx.doi.org/10.3389/fonc.2021.765399 |
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