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Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study
BACKGROUND: Up to 6-months oxaliplatin-containing regimen is now widely accepted as a standard adjuvant chemotherapy for stage III colorectal cancer (CRC). However, oral fluoropyrimidine monotherapy is used for some part of patients, especially in Asian countries including Japan, and its optimal dur...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461756/ https://www.ncbi.nlm.nih.gov/pubmed/30833647 http://dx.doi.org/10.1038/s41416-019-0410-0 |
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author | Tomita, Naohiro Kunieda, Katsuyuki Maeda, Atsuyuki Hamada, Chikuma Yamanaka, Takeharu Sato, Toshihiko Yoshida, Kazuhiro Boku, Narikazu Nezu, Riichiro Yamaguchi, Shigeki Mishima, Hideyuki Sadahiro, Sotaro Muro, Kei Ishiguro, Megumi Sakamoto, Junichi Saji, Shigetoyo Maehara, Yoshihiko |
author_facet | Tomita, Naohiro Kunieda, Katsuyuki Maeda, Atsuyuki Hamada, Chikuma Yamanaka, Takeharu Sato, Toshihiko Yoshida, Kazuhiro Boku, Narikazu Nezu, Riichiro Yamaguchi, Shigeki Mishima, Hideyuki Sadahiro, Sotaro Muro, Kei Ishiguro, Megumi Sakamoto, Junichi Saji, Shigetoyo Maehara, Yoshihiko |
author_sort | Tomita, Naohiro |
collection | PubMed |
description | BACKGROUND: Up to 6-months oxaliplatin-containing regimen is now widely accepted as a standard adjuvant chemotherapy for stage III colorectal cancer (CRC). However, oral fluoropyrimidine monotherapy is used for some part of patients, especially in Asian countries including Japan, and its optimal duration is yet to be fully investigated. METHODS: A total of 1306 patients with curatively-resected stage III CRC were randomly assigned to receive capecitabine (2500 mg/m(2)/day) for 14 out of 21 days for 6 (n = 654) or 12 (n = 650) months. The primary endpoint was disease-free survival (DFS), and the secondary endpoints were relapse-free survival (RFS), overall survival (OS), and adverse events. RESULTS: The 3- and 5-year DFS were 70.0% and 65.3% in the 6M group and 75.3% and 68.7% in the 12M group, respectively (p = 0.0549, HR = 0.858, 90% CI: 0.732–1.004). The 5-year RFS was 69.3% and 74.1% in the 6M and 12M groups, respectively (p = 0.0143, HR = 0.796, 90% CI: 0.670–0.945). The 5-year OS was 83.2% and 87.6%, respectively (p = 0.0124, HR = 0.727, 90% CI: 0.575–0.919). The incidence of overall grade 3–4 adverse events was almost comparable in both groups. CONCLUSIONS: Although 12-month adjuvant capecitabine did not demonstrate superior DFS to that of 6-month, the observed better RFS and OS in the 12-month treatment period could be of value in selected cases. |
format | Online Article Text |
id | pubmed-6461756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64617562019-09-11 Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study Tomita, Naohiro Kunieda, Katsuyuki Maeda, Atsuyuki Hamada, Chikuma Yamanaka, Takeharu Sato, Toshihiko Yoshida, Kazuhiro Boku, Narikazu Nezu, Riichiro Yamaguchi, Shigeki Mishima, Hideyuki Sadahiro, Sotaro Muro, Kei Ishiguro, Megumi Sakamoto, Junichi Saji, Shigetoyo Maehara, Yoshihiko Br J Cancer Article BACKGROUND: Up to 6-months oxaliplatin-containing regimen is now widely accepted as a standard adjuvant chemotherapy for stage III colorectal cancer (CRC). However, oral fluoropyrimidine monotherapy is used for some part of patients, especially in Asian countries including Japan, and its optimal duration is yet to be fully investigated. METHODS: A total of 1306 patients with curatively-resected stage III CRC were randomly assigned to receive capecitabine (2500 mg/m(2)/day) for 14 out of 21 days for 6 (n = 654) or 12 (n = 650) months. The primary endpoint was disease-free survival (DFS), and the secondary endpoints were relapse-free survival (RFS), overall survival (OS), and adverse events. RESULTS: The 3- and 5-year DFS were 70.0% and 65.3% in the 6M group and 75.3% and 68.7% in the 12M group, respectively (p = 0.0549, HR = 0.858, 90% CI: 0.732–1.004). The 5-year RFS was 69.3% and 74.1% in the 6M and 12M groups, respectively (p = 0.0143, HR = 0.796, 90% CI: 0.670–0.945). The 5-year OS was 83.2% and 87.6%, respectively (p = 0.0124, HR = 0.727, 90% CI: 0.575–0.919). The incidence of overall grade 3–4 adverse events was almost comparable in both groups. CONCLUSIONS: Although 12-month adjuvant capecitabine did not demonstrate superior DFS to that of 6-month, the observed better RFS and OS in the 12-month treatment period could be of value in selected cases. Nature Publishing Group UK 2019-03-05 2019-04-02 /pmc/articles/PMC6461756/ /pubmed/30833647 http://dx.doi.org/10.1038/s41416-019-0410-0 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by/4.0/Open Access 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tomita, Naohiro Kunieda, Katsuyuki Maeda, Atsuyuki Hamada, Chikuma Yamanaka, Takeharu Sato, Toshihiko Yoshida, Kazuhiro Boku, Narikazu Nezu, Riichiro Yamaguchi, Shigeki Mishima, Hideyuki Sadahiro, Sotaro Muro, Kei Ishiguro, Megumi Sakamoto, Junichi Saji, Shigetoyo Maehara, Yoshihiko Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title | Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title_full | Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title_fullStr | Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title_full_unstemmed | Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title_short | Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study |
title_sort | phase iii randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage iii colon cancer: final results of the jfmc37-0801 study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461756/ https://www.ncbi.nlm.nih.gov/pubmed/30833647 http://dx.doi.org/10.1038/s41416-019-0410-0 |
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