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Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma

PURPOSE: Permanent interstitial brachytherapy is an appealing treatment modality for patients with locoregional recurrent, resectable head and neck carcinoma (HNC), having previously received radiation. Cesium-131 ((131)Cs) is a permanent implant brachytherapy isotope, with a low average photon ener...

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Autores principales: Bar-Ad, Voichita, Hubley, Emily, Luginbuhl, Adam, Cognetti, David, Curry, Joseph, Harrison, Amy S, Johnson, Jennifer M, Keller, James, Peng, Cheng, To, David, Doyle, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701381/
https://www.ncbi.nlm.nih.gov/pubmed/31435429
http://dx.doi.org/10.5114/jcb.2019.85778
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author Bar-Ad, Voichita
Hubley, Emily
Luginbuhl, Adam
Cognetti, David
Curry, Joseph
Harrison, Amy S
Johnson, Jennifer M
Keller, James
Peng, Cheng
To, David
Doyle, Laura
author_facet Bar-Ad, Voichita
Hubley, Emily
Luginbuhl, Adam
Cognetti, David
Curry, Joseph
Harrison, Amy S
Johnson, Jennifer M
Keller, James
Peng, Cheng
To, David
Doyle, Laura
author_sort Bar-Ad, Voichita
collection PubMed
description PURPOSE: Permanent interstitial brachytherapy is an appealing treatment modality for patients with locoregional recurrent, resectable head and neck carcinoma (HNC), having previously received radiation. Cesium-131 ((131)Cs) is a permanent implant brachytherapy isotope, with a low average photon energy of 30 keV and a short half-life of 9.7 days. Exposure to medical staff and family members is low; patient isolation and patient room shielding are not required. This work presents a single institution’s implementation process of utilizing an intraoperative, permanent (131)Cs implant for patients with completely resected recurrent HNC. MATERIAL AND METHODS: Fifteen patients receiving (131)Cs permanent seed brachytherapy were included in this analysis. The process of pre-planning, selecting the dose prescription, seed ordering, intraoperative procedures, post-implant planning, and radiation safety protocols are described. RESULTS: Tumor volumes were contoured on the available preoperative PET/CT scans and a pre-implant treatment plan was created using uniform source strength and uniform 1 cm seed spacing. Implants were performed intraoperatively, following tumor resection. In five of the fifteen cases, intraoperative findings necessitated a change from the planned number of seeds and recalculation of the pre-implant plan. The average prescription dose was 56.1 ±6.6 Gy (range, 40-60 Gy). The average seed strength used was 2.2 ±0.2 U (3.5 ±0.3 mCi). Patients returned to a recovery room on a standard surgical floor and remained inpatients, without radiation safety restrictions, based on standard surgical recovery protocols. A post-implant treatment plan was generated based on immediate post-operative CT imaging to verify the seed distribution and confirm delivery of the prescription dose. Patients were provided educational information regarding radiation safety recommendations. CONCLUSIONS: Cesium-131 interstitial brachytherapy is feasible and does not pose major radiation safety concerns; it should be considered as a treatment option for previously irradiated patients with recurrent, resectable HNC.
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spelling pubmed-67013812019-08-21 Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma Bar-Ad, Voichita Hubley, Emily Luginbuhl, Adam Cognetti, David Curry, Joseph Harrison, Amy S Johnson, Jennifer M Keller, James Peng, Cheng To, David Doyle, Laura J Contemp Brachytherapy Original Paper PURPOSE: Permanent interstitial brachytherapy is an appealing treatment modality for patients with locoregional recurrent, resectable head and neck carcinoma (HNC), having previously received radiation. Cesium-131 ((131)Cs) is a permanent implant brachytherapy isotope, with a low average photon energy of 30 keV and a short half-life of 9.7 days. Exposure to medical staff and family members is low; patient isolation and patient room shielding are not required. This work presents a single institution’s implementation process of utilizing an intraoperative, permanent (131)Cs implant for patients with completely resected recurrent HNC. MATERIAL AND METHODS: Fifteen patients receiving (131)Cs permanent seed brachytherapy were included in this analysis. The process of pre-planning, selecting the dose prescription, seed ordering, intraoperative procedures, post-implant planning, and radiation safety protocols are described. RESULTS: Tumor volumes were contoured on the available preoperative PET/CT scans and a pre-implant treatment plan was created using uniform source strength and uniform 1 cm seed spacing. Implants were performed intraoperatively, following tumor resection. In five of the fifteen cases, intraoperative findings necessitated a change from the planned number of seeds and recalculation of the pre-implant plan. The average prescription dose was 56.1 ±6.6 Gy (range, 40-60 Gy). The average seed strength used was 2.2 ±0.2 U (3.5 ±0.3 mCi). Patients returned to a recovery room on a standard surgical floor and remained inpatients, without radiation safety restrictions, based on standard surgical recovery protocols. A post-implant treatment plan was generated based on immediate post-operative CT imaging to verify the seed distribution and confirm delivery of the prescription dose. Patients were provided educational information regarding radiation safety recommendations. CONCLUSIONS: Cesium-131 interstitial brachytherapy is feasible and does not pose major radiation safety concerns; it should be considered as a treatment option for previously irradiated patients with recurrent, resectable HNC. Termedia Publishing House 2019-06-28 2019-06 /pmc/articles/PMC6701381/ /pubmed/31435429 http://dx.doi.org/10.5114/jcb.2019.85778 Text en Copyright: © 2019 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Bar-Ad, Voichita
Hubley, Emily
Luginbuhl, Adam
Cognetti, David
Curry, Joseph
Harrison, Amy S
Johnson, Jennifer M
Keller, James
Peng, Cheng
To, David
Doyle, Laura
Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title_full Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title_fullStr Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title_full_unstemmed Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title_short Single institution implementation of permanent (131)Cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
title_sort single institution implementation of permanent (131)cs interstitial brachytherapy for previously irradiated patients with resectable recurrent head and neck carcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701381/
https://www.ncbi.nlm.nih.gov/pubmed/31435429
http://dx.doi.org/10.5114/jcb.2019.85778
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