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Combined modality chemoradiation in elderly oesophageal cancer patients

We present a single institution experience with 5-FU, mitomycin-C based chemoradiation for the primary treatment of elderly patients with oesophageal cancer. Twenty-five patients with a median age of 77 years (range 66–88) with a diagnosis of stage II–III squamous cell or adenocarcinoma of the oesop...

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Autores principales: Anderson, S E, Minsky, B D, Bains, M, Hummer, A, Kelsen, D, Ilson, D H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359964/
https://www.ncbi.nlm.nih.gov/pubmed/17533399
http://dx.doi.org/10.1038/sj.bjc.6603821
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author Anderson, S E
Minsky, B D
Bains, M
Hummer, A
Kelsen, D
Ilson, D H
author_facet Anderson, S E
Minsky, B D
Bains, M
Hummer, A
Kelsen, D
Ilson, D H
author_sort Anderson, S E
collection PubMed
description We present a single institution experience with 5-FU, mitomycin-C based chemoradiation for the primary treatment of elderly patients with oesophageal cancer. Twenty-five patients with a median age of 77 years (range 66–88) with a diagnosis of stage II–III squamous cell or adenocarcinoma of the oesophagus were treated at Memorial Sloan Kettering from 1996 to 2001 with two cycles of concurrent 5-FU, mitomycin-C and 50.4 Gy. Owing to age and comorbidity, these patients were not considered surgical candidates. The Charlson comorbidity score was used to evaluate patient comorbidity. Nine patients (36%) experienced grade 3–4 haematologic toxicity. Of the 23 patients evaluable for response, 17 patients (68%) had a negative post-treatment endoscopy and CT scan without evidence of progressive disease. Eleven patients (44%) are alive and 10 (40%) remain without evidence of recurrent or progressive oesophageal cancer at a median follow-up of 35 months. The median overall survival was 35 months and 2-year survival 64%. There was no significant difference in overall survival between Charlson score ⩽2 and those with a score ⩾2 (P=0.10). Similar survival was observed for patients with adenocarcinoma or squamous carcinoma. Primary chemoradiation with two cycles of 5-FU, mitomycin-C, and 50.4 Gy in elderly patients is an active regimen with moderate toxicity, despite the advanced age and heavy comorbidity burden of this cohort. Patients with local/regional oesophageal cancer with adequate functional status should not be excluded from potentially curative treatment based on age alone.
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spelling pubmed-23599642009-09-10 Combined modality chemoradiation in elderly oesophageal cancer patients Anderson, S E Minsky, B D Bains, M Hummer, A Kelsen, D Ilson, D H Br J Cancer Clinical Study We present a single institution experience with 5-FU, mitomycin-C based chemoradiation for the primary treatment of elderly patients with oesophageal cancer. Twenty-five patients with a median age of 77 years (range 66–88) with a diagnosis of stage II–III squamous cell or adenocarcinoma of the oesophagus were treated at Memorial Sloan Kettering from 1996 to 2001 with two cycles of concurrent 5-FU, mitomycin-C and 50.4 Gy. Owing to age and comorbidity, these patients were not considered surgical candidates. The Charlson comorbidity score was used to evaluate patient comorbidity. Nine patients (36%) experienced grade 3–4 haematologic toxicity. Of the 23 patients evaluable for response, 17 patients (68%) had a negative post-treatment endoscopy and CT scan without evidence of progressive disease. Eleven patients (44%) are alive and 10 (40%) remain without evidence of recurrent or progressive oesophageal cancer at a median follow-up of 35 months. The median overall survival was 35 months and 2-year survival 64%. There was no significant difference in overall survival between Charlson score ⩽2 and those with a score ⩾2 (P=0.10). Similar survival was observed for patients with adenocarcinoma or squamous carcinoma. Primary chemoradiation with two cycles of 5-FU, mitomycin-C, and 50.4 Gy in elderly patients is an active regimen with moderate toxicity, despite the advanced age and heavy comorbidity burden of this cohort. Patients with local/regional oesophageal cancer with adequate functional status should not be excluded from potentially curative treatment based on age alone. Nature Publishing Group 2007-06-18 2007-05-29 /pmc/articles/PMC2359964/ /pubmed/17533399 http://dx.doi.org/10.1038/sj.bjc.6603821 Text en Copyright © 2007 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Anderson, S E
Minsky, B D
Bains, M
Hummer, A
Kelsen, D
Ilson, D H
Combined modality chemoradiation in elderly oesophageal cancer patients
title Combined modality chemoradiation in elderly oesophageal cancer patients
title_full Combined modality chemoradiation in elderly oesophageal cancer patients
title_fullStr Combined modality chemoradiation in elderly oesophageal cancer patients
title_full_unstemmed Combined modality chemoradiation in elderly oesophageal cancer patients
title_short Combined modality chemoradiation in elderly oesophageal cancer patients
title_sort combined modality chemoradiation in elderly oesophageal cancer patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359964/
https://www.ncbi.nlm.nih.gov/pubmed/17533399
http://dx.doi.org/10.1038/sj.bjc.6603821
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