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Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases

During the past decade, tumor bed stereotactic radiosurgery (SRS) after surgical resection has been increasingly utilized in the management of brain metastases. SRS has risen as an alternative to adjuvant whole brain radiation therapy (WBRT), which has been shown in several studies to be associated...

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Autores principales: Marchan, Eduardo M., Peterson, Jennifer, Sio, Terence T., Chaichana, Kaisorn L., Harrell, Anna C., Ruiz-Garcia, Henry, Mahajan, Anita, Brown, Paul D., Trifiletti, Daniel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127288/
https://www.ncbi.nlm.nih.gov/pubmed/30234013
http://dx.doi.org/10.3389/fonc.2018.00342
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author Marchan, Eduardo M.
Peterson, Jennifer
Sio, Terence T.
Chaichana, Kaisorn L.
Harrell, Anna C.
Ruiz-Garcia, Henry
Mahajan, Anita
Brown, Paul D.
Trifiletti, Daniel M.
author_facet Marchan, Eduardo M.
Peterson, Jennifer
Sio, Terence T.
Chaichana, Kaisorn L.
Harrell, Anna C.
Ruiz-Garcia, Henry
Mahajan, Anita
Brown, Paul D.
Trifiletti, Daniel M.
author_sort Marchan, Eduardo M.
collection PubMed
description During the past decade, tumor bed stereotactic radiosurgery (SRS) after surgical resection has been increasingly utilized in the management of brain metastases. SRS has risen as an alternative to adjuvant whole brain radiation therapy (WBRT), which has been shown in several studies to be associated with increased neurotoxicity. Multiple recent articles have shown favorable local control rates compared to those of WBRT. Specifically, improvements in local control can be achieved by adding a 2 mm margin around the resection cavity. Risk factors that have been established as increasing the risk of local recurrence after resection include: subtotal resection, larger treatment volume, lower margin dose, and a long delay between surgery and SRS (>3 weeks). Moreover, consensus among experts in the field have established the importance of (a) fusion of the pre-operative magnetic resonance imaging scan to aid in volume delineation (b) contouring the entire surgical tract and (c) expanding the target to include possible microscopic disease that may extend to meningeal or venous sinus territory. These strategies can minimize the risks of symptomatic radiation-induced injury and leptomeningeal dissemination after postoperative SRS. Emerging data has arisen suggesting that multifraction postoperative SRS, or alternatively, preoperative SRS could provide decreased rates of radiation necrosis and leptomeningeal disease. Future prospective randomized clinical trials comparing outcomes between these techniques are necessary in order to improve outcomes in these patients.
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spelling pubmed-61272882018-09-19 Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases Marchan, Eduardo M. Peterson, Jennifer Sio, Terence T. Chaichana, Kaisorn L. Harrell, Anna C. Ruiz-Garcia, Henry Mahajan, Anita Brown, Paul D. Trifiletti, Daniel M. Front Oncol Oncology During the past decade, tumor bed stereotactic radiosurgery (SRS) after surgical resection has been increasingly utilized in the management of brain metastases. SRS has risen as an alternative to adjuvant whole brain radiation therapy (WBRT), which has been shown in several studies to be associated with increased neurotoxicity. Multiple recent articles have shown favorable local control rates compared to those of WBRT. Specifically, improvements in local control can be achieved by adding a 2 mm margin around the resection cavity. Risk factors that have been established as increasing the risk of local recurrence after resection include: subtotal resection, larger treatment volume, lower margin dose, and a long delay between surgery and SRS (>3 weeks). Moreover, consensus among experts in the field have established the importance of (a) fusion of the pre-operative magnetic resonance imaging scan to aid in volume delineation (b) contouring the entire surgical tract and (c) expanding the target to include possible microscopic disease that may extend to meningeal or venous sinus territory. These strategies can minimize the risks of symptomatic radiation-induced injury and leptomeningeal dissemination after postoperative SRS. Emerging data has arisen suggesting that multifraction postoperative SRS, or alternatively, preoperative SRS could provide decreased rates of radiation necrosis and leptomeningeal disease. Future prospective randomized clinical trials comparing outcomes between these techniques are necessary in order to improve outcomes in these patients. Frontiers Media S.A. 2018-08-31 /pmc/articles/PMC6127288/ /pubmed/30234013 http://dx.doi.org/10.3389/fonc.2018.00342 Text en Copyright © 2018 Marchan, Peterson, Sio, Chaichana, Harrell, Ruiz-Garcia, Mahajan, Brown and Trifiletti. http://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
Marchan, Eduardo M.
Peterson, Jennifer
Sio, Terence T.
Chaichana, Kaisorn L.
Harrell, Anna C.
Ruiz-Garcia, Henry
Mahajan, Anita
Brown, Paul D.
Trifiletti, Daniel M.
Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title_full Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title_fullStr Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title_full_unstemmed Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title_short Postoperative Cavity Stereotactic Radiosurgery for Brain Metastases
title_sort postoperative cavity stereotactic radiosurgery for brain metastases
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127288/
https://www.ncbi.nlm.nih.gov/pubmed/30234013
http://dx.doi.org/10.3389/fonc.2018.00342
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