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Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma
PURPOSE: To evaluate toxicity and clinical outcomes in patients with eyelid tumour treated with contact high-dose-rate brachytherapy (HDR-BT). MATERIAL AND METHODS: Between April 2010 and August 2017, 10 consecutive patients with tumour of the eyelid underwent contact HDR-BT and custom-made surface...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854866/ https://www.ncbi.nlm.nih.gov/pubmed/31749853 http://dx.doi.org/10.5114/jcb.2019.88619 |
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author | Vavassori, Andrea Riva, Giulia Durante, Stefano Fodor, Cristiana Comi, Stefania Cambria, Raffaella Cattani, Federica Spadola, Giuseppe Orecchia, Roberto Jereczek-Fossa, Barbara Alicja |
author_facet | Vavassori, Andrea Riva, Giulia Durante, Stefano Fodor, Cristiana Comi, Stefania Cambria, Raffaella Cattani, Federica Spadola, Giuseppe Orecchia, Roberto Jereczek-Fossa, Barbara Alicja |
author_sort | Vavassori, Andrea |
collection | PubMed |
description | PURPOSE: To evaluate toxicity and clinical outcomes in patients with eyelid tumour treated with contact high-dose-rate brachytherapy (HDR-BT). MATERIAL AND METHODS: Between April 2010 and August 2017, 10 consecutive patients with tumour of the eyelid underwent contact HDR-BT and custom-made surface mould. Every applicator was manually built using conventional thermoplastic material and standard plastic catheters. The median dose prescribed was 42 Gy (range, 30-48) with a median dose per fraction of 3.5 Gy (range, 2-4.5). The dose was delivered in a median of 12 fractions (range, 10-17) over a median of 16 days. In all cases, an ocular shield was placed to reduce the dose to the eye. Acute and late toxicity was evaluated according to RTOG toxicity criteria. RESULTS: We analyzed data of 9 of 10 patients (one patient was excluded because he did not give consent for investigation). The median age was 68 years (range, 31-88). According to the TNM-UICC staging system, 4, 1 and 4 patients were stage IA, IB and IC, respectively. Basal cell and sebaceous gland carcinomas were reported in 5 and 2 patients, respectively; other histological types were non-Hodgkin lymphoma and plasmacytoma. After a median follow-up of 51 months (range, 16-90), there was no evidence of local or distant recurrence. The treatment was very well tolerated. Most commonly acute reactions consisted of low grade (G1-G2) conjunctivitis and skin erythema. Only one patient required a temporary interruption of the treatment due to acute G2 conjunctivitis and G3 lid erythema. Only one G2 late toxicity was reported (corneal ulceration), without resulting in functional impairment or blindness. CONCLUSIONS: Our results suggest that contact HDR-BT with a customized applicator is safe, effective and offers very good local control and can be considered for the treatment of eyelid tumours. |
format | Online Article Text |
id | pubmed-6854866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-68548662019-11-20 Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma Vavassori, Andrea Riva, Giulia Durante, Stefano Fodor, Cristiana Comi, Stefania Cambria, Raffaella Cattani, Federica Spadola, Giuseppe Orecchia, Roberto Jereczek-Fossa, Barbara Alicja J Contemp Brachytherapy Original Paper PURPOSE: To evaluate toxicity and clinical outcomes in patients with eyelid tumour treated with contact high-dose-rate brachytherapy (HDR-BT). MATERIAL AND METHODS: Between April 2010 and August 2017, 10 consecutive patients with tumour of the eyelid underwent contact HDR-BT and custom-made surface mould. Every applicator was manually built using conventional thermoplastic material and standard plastic catheters. The median dose prescribed was 42 Gy (range, 30-48) with a median dose per fraction of 3.5 Gy (range, 2-4.5). The dose was delivered in a median of 12 fractions (range, 10-17) over a median of 16 days. In all cases, an ocular shield was placed to reduce the dose to the eye. Acute and late toxicity was evaluated according to RTOG toxicity criteria. RESULTS: We analyzed data of 9 of 10 patients (one patient was excluded because he did not give consent for investigation). The median age was 68 years (range, 31-88). According to the TNM-UICC staging system, 4, 1 and 4 patients were stage IA, IB and IC, respectively. Basal cell and sebaceous gland carcinomas were reported in 5 and 2 patients, respectively; other histological types were non-Hodgkin lymphoma and plasmacytoma. After a median follow-up of 51 months (range, 16-90), there was no evidence of local or distant recurrence. The treatment was very well tolerated. Most commonly acute reactions consisted of low grade (G1-G2) conjunctivitis and skin erythema. Only one patient required a temporary interruption of the treatment due to acute G2 conjunctivitis and G3 lid erythema. Only one G2 late toxicity was reported (corneal ulceration), without resulting in functional impairment or blindness. CONCLUSIONS: Our results suggest that contact HDR-BT with a customized applicator is safe, effective and offers very good local control and can be considered for the treatment of eyelid tumours. Termedia Publishing House 2019-10-30 2019-10 /pmc/articles/PMC6854866/ /pubmed/31749853 http://dx.doi.org/10.5114/jcb.2019.88619 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 Vavassori, Andrea Riva, Giulia Durante, Stefano Fodor, Cristiana Comi, Stefania Cambria, Raffaella Cattani, Federica Spadola, Giuseppe Orecchia, Roberto Jereczek-Fossa, Barbara Alicja Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title | Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title_full | Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title_fullStr | Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title_full_unstemmed | Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title_short | Mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
title_sort | mould-based surface high-dose-rate brachytherapy for eyelid carcinoma |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854866/ https://www.ncbi.nlm.nih.gov/pubmed/31749853 http://dx.doi.org/10.5114/jcb.2019.88619 |
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