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Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study

BACKGROUND: A prospective study was performed on the use of chemoradiotherapy (CRT) for esophageal cancer (EC) with involved‐field radiation therapy (IFRT), based on 18‐fluorodeoxyglucose positron‐emission tomography. Prognostic factors for overall survival (OS) were analyzed. METHODS: Eligible pati...

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Autores principales: Yamashita, Hideomi, Takenaka, Ryousuke, Okuma, Kae, Ootomo, Kuni, Nakagawa, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129562/
https://www.ncbi.nlm.nih.gov/pubmed/27766787
http://dx.doi.org/10.1111/1759-7714.12369
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author Yamashita, Hideomi
Takenaka, Ryousuke
Okuma, Kae
Ootomo, Kuni
Nakagawa, Keiichi
author_facet Yamashita, Hideomi
Takenaka, Ryousuke
Okuma, Kae
Ootomo, Kuni
Nakagawa, Keiichi
author_sort Yamashita, Hideomi
collection PubMed
description BACKGROUND: A prospective study was performed on the use of chemoradiotherapy (CRT) for esophageal cancer (EC) with involved‐field radiation therapy (IFRT), based on 18‐fluorodeoxyglucose positron‐emission tomography. Prognostic factors for overall survival (OS) were analyzed. METHODS: Eligible patients included 63 adults with newly diagnosed, untreated, inoperable stage I–IV EC with lymph node metastases. Patients received 80 mg/m(2) nedaplatin per day on day 1, 800 mg/m(2) 5‐fluorouracil on days 1–4 intravenously repeated every 28 days for two to four cycles, and combined IFRT. Irradiation was applied only to the primary tumor and positive lymph nodes. RESULTS: Three‐year progression‐free survival and OS rates were 44.9% and 47.5%, respectively. The median survival time was 31.5 months. In univariate analyses for OS, Karnofsy Performance Scale <90% (P = 0.027), initial stage (P = 0.0087), T stage (P = 0.066), N stage (P = 0.000086), M stage of M1 (P = 0.0042), dysphagia score (P = 0.00017), tumor marker squamous cell carcinoma antigen >1.5 ng/mL (P = 0.0054), gross tumor volume (GTV) > 60 cc (P = 0.00011), and relative dose intensity (RDI) of chemotherapy ≤50% (P = 0.063) were found to be associated with significantly or marginally worse OS. In multivariate analyses for OS, GTV ≥ 60 cc (P = 0.00040), RDI < 50% (P = 0.00034), and cN2‐3 (P = 0.0020) were associated with significantly worse OS. CONCLUSION: GTV, RDI and N grading, were associated with OS after definitive CRT using IFRT for EC.
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spelling pubmed-51295622016-12-12 Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study Yamashita, Hideomi Takenaka, Ryousuke Okuma, Kae Ootomo, Kuni Nakagawa, Keiichi Thorac Cancer Original Articles BACKGROUND: A prospective study was performed on the use of chemoradiotherapy (CRT) for esophageal cancer (EC) with involved‐field radiation therapy (IFRT), based on 18‐fluorodeoxyglucose positron‐emission tomography. Prognostic factors for overall survival (OS) were analyzed. METHODS: Eligible patients included 63 adults with newly diagnosed, untreated, inoperable stage I–IV EC with lymph node metastases. Patients received 80 mg/m(2) nedaplatin per day on day 1, 800 mg/m(2) 5‐fluorouracil on days 1–4 intravenously repeated every 28 days for two to four cycles, and combined IFRT. Irradiation was applied only to the primary tumor and positive lymph nodes. RESULTS: Three‐year progression‐free survival and OS rates were 44.9% and 47.5%, respectively. The median survival time was 31.5 months. In univariate analyses for OS, Karnofsy Performance Scale <90% (P = 0.027), initial stage (P = 0.0087), T stage (P = 0.066), N stage (P = 0.000086), M stage of M1 (P = 0.0042), dysphagia score (P = 0.00017), tumor marker squamous cell carcinoma antigen >1.5 ng/mL (P = 0.0054), gross tumor volume (GTV) > 60 cc (P = 0.00011), and relative dose intensity (RDI) of chemotherapy ≤50% (P = 0.063) were found to be associated with significantly or marginally worse OS. In multivariate analyses for OS, GTV ≥ 60 cc (P = 0.00040), RDI < 50% (P = 0.00034), and cN2‐3 (P = 0.0020) were associated with significantly worse OS. CONCLUSION: GTV, RDI and N grading, were associated with OS after definitive CRT using IFRT for EC. John Wiley & Sons Australia, Ltd 2016-06-02 2016-09 /pmc/articles/PMC5129562/ /pubmed/27766787 http://dx.doi.org/10.1111/1759-7714.12369 Text en © 2016 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Yamashita, Hideomi
Takenaka, Ryousuke
Okuma, Kae
Ootomo, Kuni
Nakagawa, Keiichi
Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title_full Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title_fullStr Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title_full_unstemmed Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title_short Prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase II study
title_sort prognostic factors in patients after definitive chemoradiation using involved‐field radiotherapy for esophageal cancer in a phase ii study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129562/
https://www.ncbi.nlm.nih.gov/pubmed/27766787
http://dx.doi.org/10.1111/1759-7714.12369
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