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Treatment outcomes of radiotherapy for anaplastic thyroid cancer
PURPOSE: Anaplastic thyroid cancer (ATC) is a rare tumor with a lethal clinical course despite aggressive multimodal therapy. Intensity-modulated radiotherapy (IMRT) may achieve a good therapeutic outcome in ATC patients, and the role of IMRT should be assessed. We retrospectively reviewed outcomes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Radiation Oncology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074067/ https://www.ncbi.nlm.nih.gov/pubmed/29983030 http://dx.doi.org/10.3857/roj.2018.00045 |
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author | Park, Jong Won Choi, Seo Hee Yoon, Hong In Lee, Jeongshim Kim, Tae Hyung Kim, Jun Won Lee, Ik Jae |
author_facet | Park, Jong Won Choi, Seo Hee Yoon, Hong In Lee, Jeongshim Kim, Tae Hyung Kim, Jun Won Lee, Ik Jae |
author_sort | Park, Jong Won |
collection | PubMed |
description | PURPOSE: Anaplastic thyroid cancer (ATC) is a rare tumor with a lethal clinical course despite aggressive multimodal therapy. Intensity-modulated radiotherapy (IMRT) may achieve a good therapeutic outcome in ATC patients, and the role of IMRT should be assessed. We retrospectively reviewed outcomes for ATC treated with three-dimensional conformal radiotherapy (3D-CRT) or IMRT to determine the optimal treatment option and explore the role of radiotherapy (RT). MATERIALS AND METHODS: Between December 2000 and December 2015, 41 patients with pathologically proven ATC received RT with a sufficient dose of ≥40 Gy. Among them, 21 patients (51%) underwent surgery before RT. Twenty-eight patients received IMRT, and 13 received 3D-CRT. Overall survival (OS) and progression-free survival (PFS), patterns of failure, and toxicity were examined. RESULTS: The median follow-up time for survivors was 38.0 months. The median and 1-year OS and PFS rates were 7.2 months and 29%, 4.5 months and 15%, respectively. Surgery significantly improved the prognosis (median OS: 10.7 vs. 3.9 months, p = 0.001; median PFS: 5.9 vs. 2.5 months, p = 0.007). IMRT showed significantly better PFS and OS than 3D-CRT, even in multivariate analysis (OS: hazard ratio [HR] = 0.30, p = 0.005; PFS: HR = 0.33, p = 0.005). Significantly higher radiation dose could be delivered with IMRT than 3D-CRT (EQD2(10) 66 vs. 60 Gy, p = 0.005). Only 2 patients had grade III dermatitis after IMRT. No other severe toxicity ≥grade III occurred. CONCLUSION: Patients with ATC showed better prognosis through multimodal treatment. Furthermore, IMRT could achieve favorable survival rates by safely delivering higher dose than 3D-CRT. |
format | Online Article Text |
id | pubmed-6074067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society for Radiation Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-60740672018-08-23 Treatment outcomes of radiotherapy for anaplastic thyroid cancer Park, Jong Won Choi, Seo Hee Yoon, Hong In Lee, Jeongshim Kim, Tae Hyung Kim, Jun Won Lee, Ik Jae Radiat Oncol J Original Article PURPOSE: Anaplastic thyroid cancer (ATC) is a rare tumor with a lethal clinical course despite aggressive multimodal therapy. Intensity-modulated radiotherapy (IMRT) may achieve a good therapeutic outcome in ATC patients, and the role of IMRT should be assessed. We retrospectively reviewed outcomes for ATC treated with three-dimensional conformal radiotherapy (3D-CRT) or IMRT to determine the optimal treatment option and explore the role of radiotherapy (RT). MATERIALS AND METHODS: Between December 2000 and December 2015, 41 patients with pathologically proven ATC received RT with a sufficient dose of ≥40 Gy. Among them, 21 patients (51%) underwent surgery before RT. Twenty-eight patients received IMRT, and 13 received 3D-CRT. Overall survival (OS) and progression-free survival (PFS), patterns of failure, and toxicity were examined. RESULTS: The median follow-up time for survivors was 38.0 months. The median and 1-year OS and PFS rates were 7.2 months and 29%, 4.5 months and 15%, respectively. Surgery significantly improved the prognosis (median OS: 10.7 vs. 3.9 months, p = 0.001; median PFS: 5.9 vs. 2.5 months, p = 0.007). IMRT showed significantly better PFS and OS than 3D-CRT, even in multivariate analysis (OS: hazard ratio [HR] = 0.30, p = 0.005; PFS: HR = 0.33, p = 0.005). Significantly higher radiation dose could be delivered with IMRT than 3D-CRT (EQD2(10) 66 vs. 60 Gy, p = 0.005). Only 2 patients had grade III dermatitis after IMRT. No other severe toxicity ≥grade III occurred. CONCLUSION: Patients with ATC showed better prognosis through multimodal treatment. Furthermore, IMRT could achieve favorable survival rates by safely delivering higher dose than 3D-CRT. The Korean Society for Radiation Oncology 2018-06 2018-06-29 /pmc/articles/PMC6074067/ /pubmed/29983030 http://dx.doi.org/10.3857/roj.2018.00045 Text en Copyright © 2018 The Korean Society for Radiation Oncology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Jong Won Choi, Seo Hee Yoon, Hong In Lee, Jeongshim Kim, Tae Hyung Kim, Jun Won Lee, Ik Jae Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title | Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title_full | Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title_fullStr | Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title_full_unstemmed | Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title_short | Treatment outcomes of radiotherapy for anaplastic thyroid cancer |
title_sort | treatment outcomes of radiotherapy for anaplastic thyroid cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074067/ https://www.ncbi.nlm.nih.gov/pubmed/29983030 http://dx.doi.org/10.3857/roj.2018.00045 |
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