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Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion
PURPOSE: To report our experience with the delivery of passively scattered proton therapy in the management of nonmelanoma skin cancers with clinical perineural invasion. MATERIALS AND METHODS: We reviewed the medical records of patients who received definitive or postoperative proton therapy for no...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Particle Therapy Co-operative Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270093/ https://www.ncbi.nlm.nih.gov/pubmed/34285954 http://dx.doi.org/10.14338/IJPT-20-00062.1 |
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author | Bryant, Curtis M. Dagan, Roi Holtzman, Adam L. Fernandes, Rui Bunnell, Anthony Mendenhall, William M. |
author_facet | Bryant, Curtis M. Dagan, Roi Holtzman, Adam L. Fernandes, Rui Bunnell, Anthony Mendenhall, William M. |
author_sort | Bryant, Curtis M. |
collection | PubMed |
description | PURPOSE: To report our experience with the delivery of passively scattered proton therapy in the management of nonmelanoma skin cancers with clinical perineural invasion. MATERIALS AND METHODS: We reviewed the medical records of patients who received definitive or postoperative proton therapy for nonmelanoma skin cancer with clinical perineural invasion at our institution and updated patient follow-up when possible. All patients were treated with curative intent with or without the delivery of concurrent systemic therapy. We report disease control rates and the rates of late toxicity among this cohort. RESULTS: Twenty-six patients treated between 2008 and 2017 were included in the analysis. Following proton therapy, the 3-year overall, cause-specific, and disease-free survival rates were 59%, 73%, and 60%, respectively. The 3-year local control, local regional control, and distant metastasis-free survival rates were 80%, 65%, and 96%, respectively. On univariate analysis, surgical resection before radiation therapy significantly improved local regional control rates at 3 years (55% versus 86%; P = .04). Grade 3+ late toxicities occurred in 13 patients (50%) and the most common toxicities included grade 3+ keratitis of the ipsilateral eye, which occurred in 4 patients (15%) and grade 3+ brain necrosis in 4 patients (15%). CONCLUSION: Proton therapy is effective in the management of nonmelanoma skin cancer with clinical perineural invasion. Although disease control and complication rates compare favorably to those previously published for photon-based radiation therapy, the risk for late toxicity is significant and patients should be appropriately counseled. |
format | Online Article Text |
id | pubmed-8270093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Particle Therapy Co-operative Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-82700932021-07-19 Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion Bryant, Curtis M. Dagan, Roi Holtzman, Adam L. Fernandes, Rui Bunnell, Anthony Mendenhall, William M. Int J Part Ther Clinical PURPOSE: To report our experience with the delivery of passively scattered proton therapy in the management of nonmelanoma skin cancers with clinical perineural invasion. MATERIALS AND METHODS: We reviewed the medical records of patients who received definitive or postoperative proton therapy for nonmelanoma skin cancer with clinical perineural invasion at our institution and updated patient follow-up when possible. All patients were treated with curative intent with or without the delivery of concurrent systemic therapy. We report disease control rates and the rates of late toxicity among this cohort. RESULTS: Twenty-six patients treated between 2008 and 2017 were included in the analysis. Following proton therapy, the 3-year overall, cause-specific, and disease-free survival rates were 59%, 73%, and 60%, respectively. The 3-year local control, local regional control, and distant metastasis-free survival rates were 80%, 65%, and 96%, respectively. On univariate analysis, surgical resection before radiation therapy significantly improved local regional control rates at 3 years (55% versus 86%; P = .04). Grade 3+ late toxicities occurred in 13 patients (50%) and the most common toxicities included grade 3+ keratitis of the ipsilateral eye, which occurred in 4 patients (15%) and grade 3+ brain necrosis in 4 patients (15%). CONCLUSION: Proton therapy is effective in the management of nonmelanoma skin cancer with clinical perineural invasion. Although disease control and complication rates compare favorably to those previously published for photon-based radiation therapy, the risk for late toxicity is significant and patients should be appropriately counseled. The Particle Therapy Co-operative Group 2021-06-25 /pmc/articles/PMC8270093/ /pubmed/34285954 http://dx.doi.org/10.14338/IJPT-20-00062.1 Text en ©Copyright 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/Distributed under Creative Commons CC-BY (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Clinical Bryant, Curtis M. Dagan, Roi Holtzman, Adam L. Fernandes, Rui Bunnell, Anthony Mendenhall, William M. Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title | Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title_full | Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title_fullStr | Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title_full_unstemmed | Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title_short | Passively Scattered Proton Therapy for Nonmelanoma Skin Cancer with Clinical Perineural Invasion |
title_sort | passively scattered proton therapy for nonmelanoma skin cancer with clinical perineural invasion |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270093/ https://www.ncbi.nlm.nih.gov/pubmed/34285954 http://dx.doi.org/10.14338/IJPT-20-00062.1 |
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