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Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy

SIMPLE SUMMARY: Chordomas are rare tumors of the embryologic spinal cord remnant. They are locally aggressive and typically managed with surgery in combination with radiation therapy. However, there is great variability in practice patterns including different radiation treatment types and approache...

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Autores principales: Redmond, Kristin J., Schaub, Stephanie K., Lo, Sheng-fu Larry, Khan, Majid, Lubelski, Daniel, Bilsky, Mark, Yamada, Yoshiya, Fehlings, Michael, Gogineni, Emile, Vajkoczy, Peter, Ringel, Florian, Meyer, Bernhard, Amin, Anubhav G., Combs, Stephanie E., Lo, Simon S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136664/
https://www.ncbi.nlm.nih.gov/pubmed/37190287
http://dx.doi.org/10.3390/cancers15082359
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author Redmond, Kristin J.
Schaub, Stephanie K.
Lo, Sheng-fu Larry
Khan, Majid
Lubelski, Daniel
Bilsky, Mark
Yamada, Yoshiya
Fehlings, Michael
Gogineni, Emile
Vajkoczy, Peter
Ringel, Florian
Meyer, Bernhard
Amin, Anubhav G.
Combs, Stephanie E.
Lo, Simon S.
author_facet Redmond, Kristin J.
Schaub, Stephanie K.
Lo, Sheng-fu Larry
Khan, Majid
Lubelski, Daniel
Bilsky, Mark
Yamada, Yoshiya
Fehlings, Michael
Gogineni, Emile
Vajkoczy, Peter
Ringel, Florian
Meyer, Bernhard
Amin, Anubhav G.
Combs, Stephanie E.
Lo, Simon S.
author_sort Redmond, Kristin J.
collection PubMed
description SIMPLE SUMMARY: Chordomas are rare tumors of the embryologic spinal cord remnant. They are locally aggressive and typically managed with surgery in combination with radiation therapy. However, there is great variability in practice patterns including different radiation treatment types and approaches, and limited high-level data to drive decision making. The purpose of this manuscript was to summarize the current literature specific to radiotherapy in the management of spine and sacral chordoma and to provide a practical guide on behalf of the Spine Tumor Academy, an international group of spinal oncology experts. ABSTRACT: Chordomas are rare tumors of the embryologic spinal cord remnant. They are locally aggressive and typically managed with surgery and either adjuvant or neoadjuvant radiation therapy. However, there is great variability in practice patterns including radiation type and fractionation regimen, and limited high-level data to drive decision making. The purpose of this manuscript was to summarize the current literature specific to radiotherapy in the management of spine and sacral chordoma and to provide practice recommendations on behalf of the Spine Tumor Academy. A systematic review of the literature was performed using the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) approach. Medline and Embase databases were utilized. The primary outcome measure was the rate of local control. A detailed review and interpretation of eligible studies is provided in the manuscript tables and text. Recommendations were defined as follows: (1) consensus: approved by >75% of experts; (2) predominant: approved by >50% of experts; (3) controversial: not approved by a majority of experts. Expert consensus supports dose escalation as critical in optimizing local control following radiation therapy for chordoma. In addition, comprehensive target volumes including sites of potential microscopic involvement improve local control compared with focal targets. Level I and high-quality multi-institutional data comparing treatment modalities, sequencing of radiation and surgery, and dose/fractionation schedules are needed to optimize patient outcomes in this locally aggressive malignancy.
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spelling pubmed-101366642023-04-28 Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy Redmond, Kristin J. Schaub, Stephanie K. Lo, Sheng-fu Larry Khan, Majid Lubelski, Daniel Bilsky, Mark Yamada, Yoshiya Fehlings, Michael Gogineni, Emile Vajkoczy, Peter Ringel, Florian Meyer, Bernhard Amin, Anubhav G. Combs, Stephanie E. Lo, Simon S. Cancers (Basel) Review SIMPLE SUMMARY: Chordomas are rare tumors of the embryologic spinal cord remnant. They are locally aggressive and typically managed with surgery in combination with radiation therapy. However, there is great variability in practice patterns including different radiation treatment types and approaches, and limited high-level data to drive decision making. The purpose of this manuscript was to summarize the current literature specific to radiotherapy in the management of spine and sacral chordoma and to provide a practical guide on behalf of the Spine Tumor Academy, an international group of spinal oncology experts. ABSTRACT: Chordomas are rare tumors of the embryologic spinal cord remnant. They are locally aggressive and typically managed with surgery and either adjuvant or neoadjuvant radiation therapy. However, there is great variability in practice patterns including radiation type and fractionation regimen, and limited high-level data to drive decision making. The purpose of this manuscript was to summarize the current literature specific to radiotherapy in the management of spine and sacral chordoma and to provide practice recommendations on behalf of the Spine Tumor Academy. A systematic review of the literature was performed using the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) approach. Medline and Embase databases were utilized. The primary outcome measure was the rate of local control. A detailed review and interpretation of eligible studies is provided in the manuscript tables and text. Recommendations were defined as follows: (1) consensus: approved by >75% of experts; (2) predominant: approved by >50% of experts; (3) controversial: not approved by a majority of experts. Expert consensus supports dose escalation as critical in optimizing local control following radiation therapy for chordoma. In addition, comprehensive target volumes including sites of potential microscopic involvement improve local control compared with focal targets. Level I and high-quality multi-institutional data comparing treatment modalities, sequencing of radiation and surgery, and dose/fractionation schedules are needed to optimize patient outcomes in this locally aggressive malignancy. MDPI 2023-04-18 /pmc/articles/PMC10136664/ /pubmed/37190287 http://dx.doi.org/10.3390/cancers15082359 Text en © 2023 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 Review
Redmond, Kristin J.
Schaub, Stephanie K.
Lo, Sheng-fu Larry
Khan, Majid
Lubelski, Daniel
Bilsky, Mark
Yamada, Yoshiya
Fehlings, Michael
Gogineni, Emile
Vajkoczy, Peter
Ringel, Florian
Meyer, Bernhard
Amin, Anubhav G.
Combs, Stephanie E.
Lo, Simon S.
Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title_full Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title_fullStr Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title_full_unstemmed Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title_short Radiotherapy for Mobile Spine and Sacral Chordoma: A Critical Review and Practical Guide from the Spine Tumor Academy
title_sort radiotherapy for mobile spine and sacral chordoma: a critical review and practical guide from the spine tumor academy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136664/
https://www.ncbi.nlm.nih.gov/pubmed/37190287
http://dx.doi.org/10.3390/cancers15082359
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