Efficacy and feasibility of S-1 plus oxaliplatin (C-SOX) for treating patients with stage III colon cancer (KSCC1303): final analysis of 3-year disease-free survival.


Journal

International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 13 08 2019
accepted: 24 02 2020
pubmed: 20 3 2020
medline: 11 8 2020
entrez: 20 3 2020
Statut: ppublish

Résumé

Adjuvant chemotherapy is an accepted treatment to improve survival rates in patients with stage III colon cancer, and regimens including oxaliplatin have been shown to be superior to those containing 5-FU alone. The purpose of this study was to examine the efficacy and feasibility of S-1 plus oxaliplatin (C-SOX) as adjuvant chemotherapy for patients with stage III colon cancer following curative resection. Patients with colon cancer who underwent curative resection were enrolled and received oral S-1 40-60 mg twice daily on days 1-14 every 3 weeks plus intravenous oxaliplatin 130 mg/m Between February 2014 and December 2014, 89 patients were enrolled. One patient was excluded from the analysis because of ineligibility, and the remaining 88 patients were included. The rate of protocol treatment completion was 72.3%. The relative dose intensity of S-1 and oxaliplatin was 72% and 76.3%, respectively. Hematological severe adverse events (Grade 3/4) were neutropenia (21.3%) and thrombocytopenia (15.7%). The most frequent symptom was diarrhea (Grade 3/4: 5.6%). The incidence of grade 2 neuropathy has decreased from 8.1 to 2.7% after 3 years of the therapy. Three-year disease-free survival rate was 73.9% (95% CI 63.8-81.9), and 3-year overall survival rate was 94.3% (95% CI 86.8-97.6) CONCLUSIONS: C-SOX is a safe and feasible adjuvant chemotherapy regimen in patients with stage III colon cancer undergoing curative resection.

Sections du résumé

BACKGROUND BACKGROUND
Adjuvant chemotherapy is an accepted treatment to improve survival rates in patients with stage III colon cancer, and regimens including oxaliplatin have been shown to be superior to those containing 5-FU alone. The purpose of this study was to examine the efficacy and feasibility of S-1 plus oxaliplatin (C-SOX) as adjuvant chemotherapy for patients with stage III colon cancer following curative resection.
METHODS METHODS
Patients with colon cancer who underwent curative resection were enrolled and received oral S-1 40-60 mg twice daily on days 1-14 every 3 weeks plus intravenous oxaliplatin 130 mg/m
RESULTS RESULTS
Between February 2014 and December 2014, 89 patients were enrolled. One patient was excluded from the analysis because of ineligibility, and the remaining 88 patients were included. The rate of protocol treatment completion was 72.3%. The relative dose intensity of S-1 and oxaliplatin was 72% and 76.3%, respectively. Hematological severe adverse events (Grade 3/4) were neutropenia (21.3%) and thrombocytopenia (15.7%). The most frequent symptom was diarrhea (Grade 3/4: 5.6%). The incidence of grade 2 neuropathy has decreased from 8.1 to 2.7% after 3 years of the therapy. Three-year disease-free survival rate was 73.9% (95% CI 63.8-81.9), and 3-year overall survival rate was 94.3% (95% CI 86.8-97.6) CONCLUSIONS: C-SOX is a safe and feasible adjuvant chemotherapy regimen in patients with stage III colon cancer undergoing curative resection.

Identifiants

pubmed: 32189156
doi: 10.1007/s10147-020-01646-5
pii: 10.1007/s10147-020-01646-5
doi:

Substances chimiques

Drug Combinations 0
Oxaliplatin 04ZR38536J
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Oxonic Acid 5VT6420TIG

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1115-1122

Références

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Auteurs

Koji Ando (K)

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Yasunori Emi (Y)

Department of Surgery, Saiseikai Fukuoka General Hospital, Fukuoka, Japan.

Nobutomo Miyanari (N)

Kumamoto Medical Center, Kumamoto, Japan.

Akihito Tsuji (A)

Department of Clinical Oncology, Faculty of Medicine, Kagawa University, Kagawa, Japan.

Kenji Sakai (K)

Department of Medical Oncology, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.

Terumitsu Sawai (T)

Graduate School of Medicine, Nagasaki University, Nagasaki, Japan.

Hiroshi Imamura (H)

Gastroenterology Center, Izumi Regional Medical Center, Kagoshima, Japan.

Shinichiro Mori (S)

Graduate School of Medicine, Kagoshima University, Kagoshima, Japan.

Shoji Tokunaga (S)

Medical Information Center, Kyushu University Hospital, Fukuoka, Japan.

Eiji Oki (E)

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. okieiji@surg2.med.kyushu-u.ac.jp.

Hiroshi Saeki (H)

Department of General Surgical Science Graduate School of Medicine, Gunma University, Gunma, Japan.

Yoshihiro Kakeji (Y)

Graduate School of Medicine, Kobe University, Hyogo, Japan.

Yoshito Akagi (Y)

Department of Surgery, Kurume University School of Medicine, Fukuoka, Japan.

Hideo Baba (H)

Department of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Yoshihiko Maehara (Y)

Kyushu Central Hospital, Fukuoka, Japan.

Masaki Mori (M)

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

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