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Radiation therapy for recurrent extrahepatic bile duct cancer

PURPOSE: More than half of patients with bile duct cancer (BDC) develop recurrence even after curative resection. Recurrent BDC has a poor prognosis, and no optimal treatment modality has been established. We therefore analyzed our experience on the survival outcomes of radiation therapy (RT) for re...

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Autores principales: Koh, Minji, Park, Jin-hong, Yoo, Changhoon, Yoon, Sang Min, Jung, Jinhong, Ryoo, Baek-Yeol, Chang, Heung-Moon, Kim, Kyu-pyo, Jeong, Jae Ho, Kim, Jong Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208553/
https://www.ncbi.nlm.nih.gov/pubmed/34133471
http://dx.doi.org/10.1371/journal.pone.0253285
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author Koh, Minji
Park, Jin-hong
Yoo, Changhoon
Yoon, Sang Min
Jung, Jinhong
Ryoo, Baek-Yeol
Chang, Heung-Moon
Kim, Kyu-pyo
Jeong, Jae Ho
Kim, Jong Hoon
author_facet Koh, Minji
Park, Jin-hong
Yoo, Changhoon
Yoon, Sang Min
Jung, Jinhong
Ryoo, Baek-Yeol
Chang, Heung-Moon
Kim, Kyu-pyo
Jeong, Jae Ho
Kim, Jong Hoon
author_sort Koh, Minji
collection PubMed
description PURPOSE: More than half of patients with bile duct cancer (BDC) develop recurrence even after curative resection. Recurrent BDC has a poor prognosis, and no optimal treatment modality has been established. We therefore analyzed our experience on the survival outcomes of radiation therapy (RT) for recurrent extrahepatic bile duct cancer (EHBDC). PATIENTS AND METHODS: We retrospectively analyzed the records of patients with recurrent EHBDC who underwent concurrent chemoradiation therapy (CCRT) or RT alone at our institution between January 2001 and June 2015. Freedom from locoregional progression (FFLP), progression-free survival (PFS), and overall survival (OS) were assessed, and univariate and multivariate analyses were performed to identify the prognostic factors. RESULTS: A total of 76 patients were included in the analysis. The median OS was 16 months and the rates of 2-year FFLP, PFS, and OS were 61%, 25%, and 33%, respectively. Among the evaluable patients, the first site of failure was the locoregional area in 16 patients, distant metastasis in 27, and both sites in 8. On univariate analysis, disease-free interval (p = 0.012) and concurrent chemotherapy (p = 0.040) were found as significant prognostic factors for OS. One patient with CCRT developed a grade 3 hematologic toxicity, and two patients experienced late grade 3 toxicities including duodenal ulcer bleeding and obstruction. CONCLUSIONS: RT for recurrent EHBDC showed favorable survival and local control with limited treatment-related toxicities. Considering that the most common pattern of failure was distant metastasis, further studies on the optimal scheme of chemotherapy and RT are warranted.
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spelling pubmed-82085532021-06-29 Radiation therapy for recurrent extrahepatic bile duct cancer Koh, Minji Park, Jin-hong Yoo, Changhoon Yoon, Sang Min Jung, Jinhong Ryoo, Baek-Yeol Chang, Heung-Moon Kim, Kyu-pyo Jeong, Jae Ho Kim, Jong Hoon PLoS One Research Article PURPOSE: More than half of patients with bile duct cancer (BDC) develop recurrence even after curative resection. Recurrent BDC has a poor prognosis, and no optimal treatment modality has been established. We therefore analyzed our experience on the survival outcomes of radiation therapy (RT) for recurrent extrahepatic bile duct cancer (EHBDC). PATIENTS AND METHODS: We retrospectively analyzed the records of patients with recurrent EHBDC who underwent concurrent chemoradiation therapy (CCRT) or RT alone at our institution between January 2001 and June 2015. Freedom from locoregional progression (FFLP), progression-free survival (PFS), and overall survival (OS) were assessed, and univariate and multivariate analyses were performed to identify the prognostic factors. RESULTS: A total of 76 patients were included in the analysis. The median OS was 16 months and the rates of 2-year FFLP, PFS, and OS were 61%, 25%, and 33%, respectively. Among the evaluable patients, the first site of failure was the locoregional area in 16 patients, distant metastasis in 27, and both sites in 8. On univariate analysis, disease-free interval (p = 0.012) and concurrent chemotherapy (p = 0.040) were found as significant prognostic factors for OS. One patient with CCRT developed a grade 3 hematologic toxicity, and two patients experienced late grade 3 toxicities including duodenal ulcer bleeding and obstruction. CONCLUSIONS: RT for recurrent EHBDC showed favorable survival and local control with limited treatment-related toxicities. Considering that the most common pattern of failure was distant metastasis, further studies on the optimal scheme of chemotherapy and RT are warranted. Public Library of Science 2021-06-16 /pmc/articles/PMC8208553/ /pubmed/34133471 http://dx.doi.org/10.1371/journal.pone.0253285 Text en © 2021 Koh et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Koh, Minji
Park, Jin-hong
Yoo, Changhoon
Yoon, Sang Min
Jung, Jinhong
Ryoo, Baek-Yeol
Chang, Heung-Moon
Kim, Kyu-pyo
Jeong, Jae Ho
Kim, Jong Hoon
Radiation therapy for recurrent extrahepatic bile duct cancer
title Radiation therapy for recurrent extrahepatic bile duct cancer
title_full Radiation therapy for recurrent extrahepatic bile duct cancer
title_fullStr Radiation therapy for recurrent extrahepatic bile duct cancer
title_full_unstemmed Radiation therapy for recurrent extrahepatic bile duct cancer
title_short Radiation therapy for recurrent extrahepatic bile duct cancer
title_sort radiation therapy for recurrent extrahepatic bile duct cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208553/
https://www.ncbi.nlm.nih.gov/pubmed/34133471
http://dx.doi.org/10.1371/journal.pone.0253285
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