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Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial

BACKGROUND: Surgery is recommended for patients with high-risk submucosal invasive rectal cancer (SM-RC) after local resection but affects the quality of life due to stoma placement or impaired anal function; therefore, alternative treatment approaches are needed to prevent local metastasis. The pur...

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Autores principales: Noguchi, Masaaki, Shitara, Kohei, Kawazoe, Akihito, Yamamoto, Daisuke, Takii, Yasumasa, Saito, Yutaka, Sato, Toshihiko, Horimatsu, Takahiro, Ishikawa, Hideki, Ito, Yoshinori, Ito, Masaaki, Ikematsu, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086053/
https://www.ncbi.nlm.nih.gov/pubmed/33558891
http://dx.doi.org/10.1093/jjco/hyaa260
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author Noguchi, Masaaki
Shitara, Kohei
Kawazoe, Akihito
Yamamoto, Daisuke
Takii, Yasumasa
Saito, Yutaka
Sato, Toshihiko
Horimatsu, Takahiro
Ishikawa, Hideki
Ito, Yoshinori
Ito, Masaaki
Ikematsu, Hiroaki
author_facet Noguchi, Masaaki
Shitara, Kohei
Kawazoe, Akihito
Yamamoto, Daisuke
Takii, Yasumasa
Saito, Yutaka
Sato, Toshihiko
Horimatsu, Takahiro
Ishikawa, Hideki
Ito, Yoshinori
Ito, Masaaki
Ikematsu, Hiroaki
author_sort Noguchi, Masaaki
collection PubMed
description BACKGROUND: Surgery is recommended for patients with high-risk submucosal invasive rectal cancer (SM-RC) after local resection but affects the quality of life due to stoma placement or impaired anal function; therefore, alternative treatment approaches are needed to prevent local metastasis. The purpose of this study was to assess the short-term safety of adjuvant chemoradiotherapy with capecitabine in patients with high-risk submucosal invasive rectal cancer after local resection. METHODS: This single-arm, multicenter, phase II trial included patients undergoing local resection for high-risk submucosal invasive rectal cancer within 12 weeks prior to enrollment. High-risk submucosal invasive rectal cancer was defined as the presence of at least one of the following factors: poor differentiation of adenocarcinoma, submucosal invasion depth > 1 mm, presence of lymphovascular invasion and grade-2 or -3 tumour budding. Protocol treatment comprised 45.0 Gy radiotherapy with conventional fractionation and 1650 mg/m(2) capecitabine given twice daily until radiotherapy completion. The primary endpoint was treatment completion rate with an expected rate of 95% and a threshold of 80%. RESULTS: Twenty-nine patients from six institutions were enrolled between May 2015 and February 2018. One patient was ineligible. Twenty-three patients completed treatment, with a completion rate of 82% (80% confidence interval, 69–91%); the remaining five patients completed treatment with protocol deviation. The median relative dose intensity of capecitabine was 100% (range, 58–100%). Common adverse events included radiation dermatitis (54%), anal pain (39%) and anal mucositis (29%). No grade-3 or higher adverse events were reported. CONCLUSIONS: Adjuvant chemoradiotherapy using capecitabine demonstrated acceptable short-term safety profiles in patients with high-risk submucosal invasive rectal cancer after local resection.
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spelling pubmed-80860532021-05-05 Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial Noguchi, Masaaki Shitara, Kohei Kawazoe, Akihito Yamamoto, Daisuke Takii, Yasumasa Saito, Yutaka Sato, Toshihiko Horimatsu, Takahiro Ishikawa, Hideki Ito, Yoshinori Ito, Masaaki Ikematsu, Hiroaki Jpn J Clin Oncol Original Article BACKGROUND: Surgery is recommended for patients with high-risk submucosal invasive rectal cancer (SM-RC) after local resection but affects the quality of life due to stoma placement or impaired anal function; therefore, alternative treatment approaches are needed to prevent local metastasis. The purpose of this study was to assess the short-term safety of adjuvant chemoradiotherapy with capecitabine in patients with high-risk submucosal invasive rectal cancer after local resection. METHODS: This single-arm, multicenter, phase II trial included patients undergoing local resection for high-risk submucosal invasive rectal cancer within 12 weeks prior to enrollment. High-risk submucosal invasive rectal cancer was defined as the presence of at least one of the following factors: poor differentiation of adenocarcinoma, submucosal invasion depth > 1 mm, presence of lymphovascular invasion and grade-2 or -3 tumour budding. Protocol treatment comprised 45.0 Gy radiotherapy with conventional fractionation and 1650 mg/m(2) capecitabine given twice daily until radiotherapy completion. The primary endpoint was treatment completion rate with an expected rate of 95% and a threshold of 80%. RESULTS: Twenty-nine patients from six institutions were enrolled between May 2015 and February 2018. One patient was ineligible. Twenty-three patients completed treatment, with a completion rate of 82% (80% confidence interval, 69–91%); the remaining five patients completed treatment with protocol deviation. The median relative dose intensity of capecitabine was 100% (range, 58–100%). Common adverse events included radiation dermatitis (54%), anal pain (39%) and anal mucositis (29%). No grade-3 or higher adverse events were reported. CONCLUSIONS: Adjuvant chemoradiotherapy using capecitabine demonstrated acceptable short-term safety profiles in patients with high-risk submucosal invasive rectal cancer after local resection. Oxford University Press 2021-02-09 /pmc/articles/PMC8086053/ /pubmed/33558891 http://dx.doi.org/10.1093/jjco/hyaa260 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Noguchi, Masaaki
Shitara, Kohei
Kawazoe, Akihito
Yamamoto, Daisuke
Takii, Yasumasa
Saito, Yutaka
Sato, Toshihiko
Horimatsu, Takahiro
Ishikawa, Hideki
Ito, Yoshinori
Ito, Masaaki
Ikematsu, Hiroaki
Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title_full Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title_fullStr Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title_full_unstemmed Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title_short Short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase II trial
title_sort short-term safety of adjuvant chemoradiotherapy after local resection for patients with high-risk submucosal invasive rectal cancer: a single-arm, multicenter phase ii trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086053/
https://www.ncbi.nlm.nih.gov/pubmed/33558891
http://dx.doi.org/10.1093/jjco/hyaa260
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