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Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer

Purpose: The aim of this study was to clarify the risk factors for discontinuing tegafur/gimeracil/oteracil potassium (S-1) adjuvant chemotherapy following gastrectomy in patients with gastric cancer. Methods: We retrospectively investigated patients with curatively-resected gastric cancer who recei...

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Autores principales: Kawazoe, Hitoshi, Shimasaki, Maya, Ueno, Masaki, Sumikawa, Satomi, Takatori, Shingo, Namba, Hiroyuki, Yoshida, Motohira, Sato, Koichi, Kojima, Yoh, Watanabe, Yuji, Moriguchi, Toshihide, Tanaka, Akihiro, Araki, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392055/
https://www.ncbi.nlm.nih.gov/pubmed/25874010
http://dx.doi.org/10.7150/jca.11189
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author Kawazoe, Hitoshi
Shimasaki, Maya
Ueno, Masaki
Sumikawa, Satomi
Takatori, Shingo
Namba, Hiroyuki
Yoshida, Motohira
Sato, Koichi
Kojima, Yoh
Watanabe, Yuji
Moriguchi, Toshihide
Tanaka, Akihiro
Araki, Hiroaki
author_facet Kawazoe, Hitoshi
Shimasaki, Maya
Ueno, Masaki
Sumikawa, Satomi
Takatori, Shingo
Namba, Hiroyuki
Yoshida, Motohira
Sato, Koichi
Kojima, Yoh
Watanabe, Yuji
Moriguchi, Toshihide
Tanaka, Akihiro
Araki, Hiroaki
author_sort Kawazoe, Hitoshi
collection PubMed
description Purpose: The aim of this study was to clarify the risk factors for discontinuing tegafur/gimeracil/oteracil potassium (S-1) adjuvant chemotherapy following gastrectomy in patients with gastric cancer. Methods: We retrospectively investigated patients with curatively-resected gastric cancer who received S-1 adjuvant chemotherapy. S-1 was administered orally at 80-120 mg/day, depending on body surface area, on days 1-28 every 6 weeks for 1 year. The dose and treatment schedule were modified at the clinicians' discretion, according to toxicity. Results: Seventy-one patients were included in the study, 26 of whom discontinued S-1 therapy. The relapse-free survival rates in the S-1-completed and S-1-discontinuation groups at 5 years post-surgery were 88.1% and 55.8%, respectively. The overall survival rates in the S-1-completed and S-1-discontinuation groups at 5 years post-surgery were 89.4% and 59.8%, respectively. The hazard ratios for relapse and death were significantly lower in the S-1-completed group compared with those in the S-1-discontinuation group (0.18; p<0.001 and 0.19; p=0.002, respectively). Multivariate logistic regression analysis revealed that S-1 discontinuation was significantly associated with an initial overdose of S-1, having stage I cancer, creatinine clearance <66 mL/min, and a side effect of nausea. Conclusions: These results suggest that assessing renal function to avoid initial overdose of S-1, together with the early management of side effects, may support the continuation of S-1 adjuvant chemotherapy in patients with gastric cancer.
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spelling pubmed-43920552015-04-13 Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer Kawazoe, Hitoshi Shimasaki, Maya Ueno, Masaki Sumikawa, Satomi Takatori, Shingo Namba, Hiroyuki Yoshida, Motohira Sato, Koichi Kojima, Yoh Watanabe, Yuji Moriguchi, Toshihide Tanaka, Akihiro Araki, Hiroaki J Cancer Research Paper Purpose: The aim of this study was to clarify the risk factors for discontinuing tegafur/gimeracil/oteracil potassium (S-1) adjuvant chemotherapy following gastrectomy in patients with gastric cancer. Methods: We retrospectively investigated patients with curatively-resected gastric cancer who received S-1 adjuvant chemotherapy. S-1 was administered orally at 80-120 mg/day, depending on body surface area, on days 1-28 every 6 weeks for 1 year. The dose and treatment schedule were modified at the clinicians' discretion, according to toxicity. Results: Seventy-one patients were included in the study, 26 of whom discontinued S-1 therapy. The relapse-free survival rates in the S-1-completed and S-1-discontinuation groups at 5 years post-surgery were 88.1% and 55.8%, respectively. The overall survival rates in the S-1-completed and S-1-discontinuation groups at 5 years post-surgery were 89.4% and 59.8%, respectively. The hazard ratios for relapse and death were significantly lower in the S-1-completed group compared with those in the S-1-discontinuation group (0.18; p<0.001 and 0.19; p=0.002, respectively). Multivariate logistic regression analysis revealed that S-1 discontinuation was significantly associated with an initial overdose of S-1, having stage I cancer, creatinine clearance <66 mL/min, and a side effect of nausea. Conclusions: These results suggest that assessing renal function to avoid initial overdose of S-1, together with the early management of side effects, may support the continuation of S-1 adjuvant chemotherapy in patients with gastric cancer. Ivyspring International Publisher 2015-03-18 /pmc/articles/PMC4392055/ /pubmed/25874010 http://dx.doi.org/10.7150/jca.11189 Text en © 2015 Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Research Paper
Kawazoe, Hitoshi
Shimasaki, Maya
Ueno, Masaki
Sumikawa, Satomi
Takatori, Shingo
Namba, Hiroyuki
Yoshida, Motohira
Sato, Koichi
Kojima, Yoh
Watanabe, Yuji
Moriguchi, Toshihide
Tanaka, Akihiro
Araki, Hiroaki
Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title_full Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title_fullStr Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title_full_unstemmed Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title_short Risk Factors for Discontinuation of S-1 Adjuvant Chemotherapy for Gastric Cancer
title_sort risk factors for discontinuation of s-1 adjuvant chemotherapy for gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392055/
https://www.ncbi.nlm.nih.gov/pubmed/25874010
http://dx.doi.org/10.7150/jca.11189
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