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A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol

BACKGROUND: Cancers of the head and neck region are often characterized by locally advanced, non-metastatic disease. Standard treatments for advanced cervico-facial cancers of the skin or primary head and neck squamous cell carcinoma (HNSCC) include combinations of surgery, radiation and chemotherap...

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Autores principales: Lee, Justin, Nguyen, Nhu Tram, Wright, James, Yeung, Ka-Kit David, Sagar, Stephen, Kim, Do-Hoon, Ostapiak, Orest, Doerwald-Munoz, Lilian, Whelan, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131380/
https://www.ncbi.nlm.nih.gov/pubmed/37098494
http://dx.doi.org/10.1186/s12885-023-10807-4
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author Lee, Justin
Nguyen, Nhu Tram
Wright, James
Yeung, Ka-Kit David
Sagar, Stephen
Kim, Do-Hoon
Ostapiak, Orest
Doerwald-Munoz, Lilian
Whelan, Timothy
author_facet Lee, Justin
Nguyen, Nhu Tram
Wright, James
Yeung, Ka-Kit David
Sagar, Stephen
Kim, Do-Hoon
Ostapiak, Orest
Doerwald-Munoz, Lilian
Whelan, Timothy
author_sort Lee, Justin
collection PubMed
description BACKGROUND: Cancers of the head and neck region are often characterized by locally advanced, non-metastatic disease. Standard treatments for advanced cervico-facial cancers of the skin or primary head and neck squamous cell carcinoma (HNSCC) include combinations of surgery, radiation and chemotherapy, which are associated with high rates of acute toxicity and complications. Stereotactic body radiotherapy (SBRT) has been shown to be a promising modality of treatment for this patient population in retrospective studies; to our knowledge, there are no prospective clinical studies evaluating the safety and efficacy of SBRT in these patients. METHODS: This phase 2, single institution, single arm study aims to evaluate response rates to SBRT in older age patients with locally advanced HNSCC for whom primary surgery is not recommended or performed. The intervention is SBRT 45 Gy in 5 fractions given every 3–4 days. Toxicity, quality of life and patient outcomes will be recorded regularly up to 24 months after completion of SBRT. DISCUSSION: For this patient population, SBRT may offer a shorter and more effective treatment than the current standard of care palliative regimens. If the study demonstrates that SBRT is safe and effective, then this may lead to randomized studies comparing conventional radiotherapy to SBRT for selected head and neck cancer patients. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04435938.  Date registered: June 17, 2020. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10807-4.
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spelling pubmed-101313802023-04-27 A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol Lee, Justin Nguyen, Nhu Tram Wright, James Yeung, Ka-Kit David Sagar, Stephen Kim, Do-Hoon Ostapiak, Orest Doerwald-Munoz, Lilian Whelan, Timothy BMC Cancer Study Protocol BACKGROUND: Cancers of the head and neck region are often characterized by locally advanced, non-metastatic disease. Standard treatments for advanced cervico-facial cancers of the skin or primary head and neck squamous cell carcinoma (HNSCC) include combinations of surgery, radiation and chemotherapy, which are associated with high rates of acute toxicity and complications. Stereotactic body radiotherapy (SBRT) has been shown to be a promising modality of treatment for this patient population in retrospective studies; to our knowledge, there are no prospective clinical studies evaluating the safety and efficacy of SBRT in these patients. METHODS: This phase 2, single institution, single arm study aims to evaluate response rates to SBRT in older age patients with locally advanced HNSCC for whom primary surgery is not recommended or performed. The intervention is SBRT 45 Gy in 5 fractions given every 3–4 days. Toxicity, quality of life and patient outcomes will be recorded regularly up to 24 months after completion of SBRT. DISCUSSION: For this patient population, SBRT may offer a shorter and more effective treatment than the current standard of care palliative regimens. If the study demonstrates that SBRT is safe and effective, then this may lead to randomized studies comparing conventional radiotherapy to SBRT for selected head and neck cancer patients. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04435938.  Date registered: June 17, 2020. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10807-4. BioMed Central 2023-04-26 /pmc/articles/PMC10131380/ /pubmed/37098494 http://dx.doi.org/10.1186/s12885-023-10807-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Lee, Justin
Nguyen, Nhu Tram
Wright, James
Yeung, Ka-Kit David
Sagar, Stephen
Kim, Do-Hoon
Ostapiak, Orest
Doerwald-Munoz, Lilian
Whelan, Timothy
A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title_full A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title_fullStr A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title_full_unstemmed A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title_short A phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (SHINE): a single arm clinical trial protocol
title_sort phase 2 study of stereotactic body radiation therapy for squamous cell carcinoma of the head and neck (shine): a single arm clinical trial protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131380/
https://www.ncbi.nlm.nih.gov/pubmed/37098494
http://dx.doi.org/10.1186/s12885-023-10807-4
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