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Efficacy of Different Number of XELOX or SOX Chemotherapy Cycles After D2 Resection for Stage III Gastric Cancer

  • Yu, Yuanyuan (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Zhang, Zicheng (School of Biomedical Engineering, Wenzhou Medical University) ;
  • Meng, Qianhao (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Wang, Ke (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Li, Qingwei (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Ma, Yue (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Yao, Yuanfei (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital) ;
  • Sun, Jie (School of Biomedical Engineering, Wenzhou Medical University) ;
  • Wang, Guangyu (Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital)
  • Received : 2021.12.12
  • Accepted : 2022.03.17
  • Published : 2022.04.30

Abstract

Purpose: We aimed to explore whether the prognosis of patients treated with capecitabine and oxaliplatin (XELOX) or S-1 and oxaliplatin (SOX) regimens who received fewer cycles of chemotherapy after D2 radical resection for gastric cancer (GC) would be non-inferior to that of patients who received the standard number of cycles of chemotherapy. Materials and Methods: Data on patients who received XELOX or SOX chemotherapy after undergoing D2 radical resection at Harbin Medical University Cancer Hospital between January 2011 and May 2016 were collected. Results: In patients who received 4, 6, and 8 cycles of chemotherapy, the 5-year overall survival (OS) rates were 59.4%, 64.8%, and 62.7%, respectively. Compared to patients who received 4 cycles of chemotherapy, those who received 6 cycles (hazard ratio [HR], 0.882; 95% confidence interval [CI], 0.599-1.299; P=0.52) or 8 cycles (HR, 0.882; 95% CI, 0.533-1.458; P=0.62) of chemotherapy did not exhibit significantly prolonged OS. The 3-year disease-free survival (DFS) rate of patients who received 4, 6, and 8 cycles of chemotherapy was 62.1%, 67.2%, and 60.8%, respectively. Compared to patients who received 4 cycles of chemotherapy, those who received 6 cycles (HR, 0.835; 95% CI, 0.572-1.221; P=0.35) or 8 cycles (HR, 0.972; 95% CI, 0.606-1.558; P=0.91) of chemotherapy did not show significantly prolonged DFS. However, the 3-year DFS and 5-year OS rates of patients who received 6 cycles of chemotherapy appeared to be superior to those of patients who received 4 and 8 cycles of chemotherapy. Conclusions: For patients with stage III GC, 4 to 6 cycles of XELOX or SOX chemotherapy may be a favorable option. This study provides a rationale for further randomized clinical trials.

Keywords

Acknowledgement

We thank Spandidos Publications for English language editing.

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