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A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer
BACKGROUND: Concurrent chemoradiotherapy (CCRT) using conventional platinum-based doublets are often associated with significant incidence of toxic effects in elderly patients with esophageal cancer. We previously reported a phase I trial of CCRT using S-1, an oral 5-fluorouracil derivative, which y...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669946/ https://www.ncbi.nlm.nih.gov/pubmed/29137320 http://dx.doi.org/10.18632/oncotarget.20938 |
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author | Ji, Yongling Du, Xianghui Tian, Ye Sheng, Liming Cheng, Lei Chen, Ying Qiu, Guoqing Zhou, Xia Bao, Wuan Zhang, Danhong Chen, Ming |
author_facet | Ji, Yongling Du, Xianghui Tian, Ye Sheng, Liming Cheng, Lei Chen, Ying Qiu, Guoqing Zhou, Xia Bao, Wuan Zhang, Danhong Chen, Ming |
author_sort | Ji, Yongling |
collection | PubMed |
description | BACKGROUND: Concurrent chemoradiotherapy (CCRT) using conventional platinum-based doublets are often associated with significant incidence of toxic effects in elderly patients with esophageal cancer. We previously reported a phase I trial of CCRT using S-1, an oral 5-fluorouracil derivative, which yielded well safe and active outcomes. METHODS: Patients with histologically confirmed esophageal cancer, who were age of 70 years or older with performance status (PS) score of 0-2 or age of 66 to 69 with PS score of 2, were eligible for this Phase II trial. Radiotherapy was delivered in 1.8 Gy per fraction to a total dose of 54 Gy. Concurrently, S-1 was administered at 70 mg/m(2) on days 1–14 and 29–42. The primary end point was 2-year overall survival rate. RESULTS: Thirty patients were enrolled, and 28 patients completed the full course of radiotherapy. No grade 4 toxicity or treatment-related death occurred. The grade 3 toxicities included esophagitis (16.7%), leucopoenia (13.3%), neutropenia (10%), anaemia (3.3%), pneumonitis (3.3%) and fatigue (3.3%). The median progression-free survival time and median survival time was 19 and 24 months, respectively. The 2-year overall survival rate was 45.1%, which exceeded the predefined threshold of 2-year OS 35% and met the primary end point of the study. CONCLUSIONS: The results suggest that CCRT using S-1 is effective with mild toxicity in elderly patients with esophageal cancer. A phase III trial is needed to further evaluate this regimen. |
format | Online Article Text |
id | pubmed-5669946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56699462017-11-09 A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer Ji, Yongling Du, Xianghui Tian, Ye Sheng, Liming Cheng, Lei Chen, Ying Qiu, Guoqing Zhou, Xia Bao, Wuan Zhang, Danhong Chen, Ming Oncotarget Research Paper BACKGROUND: Concurrent chemoradiotherapy (CCRT) using conventional platinum-based doublets are often associated with significant incidence of toxic effects in elderly patients with esophageal cancer. We previously reported a phase I trial of CCRT using S-1, an oral 5-fluorouracil derivative, which yielded well safe and active outcomes. METHODS: Patients with histologically confirmed esophageal cancer, who were age of 70 years or older with performance status (PS) score of 0-2 or age of 66 to 69 with PS score of 2, were eligible for this Phase II trial. Radiotherapy was delivered in 1.8 Gy per fraction to a total dose of 54 Gy. Concurrently, S-1 was administered at 70 mg/m(2) on days 1–14 and 29–42. The primary end point was 2-year overall survival rate. RESULTS: Thirty patients were enrolled, and 28 patients completed the full course of radiotherapy. No grade 4 toxicity or treatment-related death occurred. The grade 3 toxicities included esophagitis (16.7%), leucopoenia (13.3%), neutropenia (10%), anaemia (3.3%), pneumonitis (3.3%) and fatigue (3.3%). The median progression-free survival time and median survival time was 19 and 24 months, respectively. The 2-year overall survival rate was 45.1%, which exceeded the predefined threshold of 2-year OS 35% and met the primary end point of the study. CONCLUSIONS: The results suggest that CCRT using S-1 is effective with mild toxicity in elderly patients with esophageal cancer. A phase III trial is needed to further evaluate this regimen. Impact Journals LLC 2017-09-15 /pmc/articles/PMC5669946/ /pubmed/29137320 http://dx.doi.org/10.18632/oncotarget.20938 Text en Copyright: © 2017 Ji et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ji, Yongling Du, Xianghui Tian, Ye Sheng, Liming Cheng, Lei Chen, Ying Qiu, Guoqing Zhou, Xia Bao, Wuan Zhang, Danhong Chen, Ming A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title | A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title_full | A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title_fullStr | A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title_full_unstemmed | A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title_short | A phase II study of S-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
title_sort | phase ii study of s-1 with concurrent radiotherapy in elderly patients with esophageal cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669946/ https://www.ncbi.nlm.nih.gov/pubmed/29137320 http://dx.doi.org/10.18632/oncotarget.20938 |
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