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Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma
BACKGROUND: Thymic carcinoma is a rare cancer with minimal evidence of a survival benefit following chemotherapy. An oral fluoropyrimidine of S-1, however, is the recommended active cytotoxic chemotherapy agent for refractory thymic carcinoma based on a case series, whereas sunitinib or everolimus a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766615/ https://www.ncbi.nlm.nih.gov/pubmed/26915359 http://dx.doi.org/10.1186/s12885-016-2159-7 |
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author | Okuma, Yusuke Hosomi, Yukio Miyamoto, Shingo Shibuya, Masahiko Okamura, Tatsuru Hishima, Tsunekazu |
author_facet | Okuma, Yusuke Hosomi, Yukio Miyamoto, Shingo Shibuya, Masahiko Okamura, Tatsuru Hishima, Tsunekazu |
author_sort | Okuma, Yusuke |
collection | PubMed |
description | BACKGROUND: Thymic carcinoma is a rare cancer with minimal evidence of a survival benefit following chemotherapy. An oral fluoropyrimidine of S-1, however, is the recommended active cytotoxic chemotherapy agent for refractory thymic carcinoma based on a case series, whereas sunitinib or everolimus are recommended as molecular-targeted agents based on Phase II trials. We retrospectively investigated the efficacy of S-1 for refractory thymic carcinoma and performed a biomarker analysis. METHODS: We assessed the clinicopathological variables of 14 consecutive patients who underwent S-1 for refractory thymic carcinoma and correlated the clinical outcomes with potential biomarkers using paraffin-embedded cancer tissues of eight patients in the cohort. RESULTS: A total of 178 thymic malignancies were identified, of whom 14 patients included 12 cases of squamous cell carcinoma, one lymphoepithelioma-like carcinoma, and one undifferentiated carcinoma. Six patients exhibited a partial response (42.9 %: 95 % confidence interval [CI], 21.4–67.4) and the disease control rate was 85.7 % (60.0–96.0 %). After a median follow-up of 24.2 months, the median progression-free survival was 8.1 months (range, 2.6–12.2 months), and median overall survival was 30.0 months (range, 6.2–41.9 months). No significant correlation between biomarker expression and response was noted. However, thymidine synthase (TS)/dihydropyrimidine dehydrogenase and TS/orotate phosphoribosyltransferase were observed. CONCLUSIONS: S-1 for refractory thymic carcinoma offered clinical activity and achieved an 85 % disease control rate. Although the biomarkers did not correlate with clinical outcome, the study results showed efficacy of S-1 as a cytotoxic chemotherapy for refractory thymic carcinoma, which warrants future investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2159-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4766615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47666152016-02-26 Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma Okuma, Yusuke Hosomi, Yukio Miyamoto, Shingo Shibuya, Masahiko Okamura, Tatsuru Hishima, Tsunekazu BMC Cancer Research Article BACKGROUND: Thymic carcinoma is a rare cancer with minimal evidence of a survival benefit following chemotherapy. An oral fluoropyrimidine of S-1, however, is the recommended active cytotoxic chemotherapy agent for refractory thymic carcinoma based on a case series, whereas sunitinib or everolimus are recommended as molecular-targeted agents based on Phase II trials. We retrospectively investigated the efficacy of S-1 for refractory thymic carcinoma and performed a biomarker analysis. METHODS: We assessed the clinicopathological variables of 14 consecutive patients who underwent S-1 for refractory thymic carcinoma and correlated the clinical outcomes with potential biomarkers using paraffin-embedded cancer tissues of eight patients in the cohort. RESULTS: A total of 178 thymic malignancies were identified, of whom 14 patients included 12 cases of squamous cell carcinoma, one lymphoepithelioma-like carcinoma, and one undifferentiated carcinoma. Six patients exhibited a partial response (42.9 %: 95 % confidence interval [CI], 21.4–67.4) and the disease control rate was 85.7 % (60.0–96.0 %). After a median follow-up of 24.2 months, the median progression-free survival was 8.1 months (range, 2.6–12.2 months), and median overall survival was 30.0 months (range, 6.2–41.9 months). No significant correlation between biomarker expression and response was noted. However, thymidine synthase (TS)/dihydropyrimidine dehydrogenase and TS/orotate phosphoribosyltransferase were observed. CONCLUSIONS: S-1 for refractory thymic carcinoma offered clinical activity and achieved an 85 % disease control rate. Although the biomarkers did not correlate with clinical outcome, the study results showed efficacy of S-1 as a cytotoxic chemotherapy for refractory thymic carcinoma, which warrants future investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2159-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-25 /pmc/articles/PMC4766615/ /pubmed/26915359 http://dx.doi.org/10.1186/s12885-016-2159-7 Text en © Okuma et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Okuma, Yusuke Hosomi, Yukio Miyamoto, Shingo Shibuya, Masahiko Okamura, Tatsuru Hishima, Tsunekazu Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title | Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title_full | Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title_fullStr | Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title_full_unstemmed | Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title_short | Correlation between S-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
title_sort | correlation between s-1 treatment outcome and expression of biomarkers for refractory thymic carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766615/ https://www.ncbi.nlm.nih.gov/pubmed/26915359 http://dx.doi.org/10.1186/s12885-016-2159-7 |
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