Evaluating the efficacy and safety of TS1 - Cisplatin regimen in the first - line treatment of advanced gastric cancer patients

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Objectives: To evaluate the efficacy and safety of the TS1-Cisplatin regimen in the first-line treatment of metastatic gastric cancer patients.

Methods: 38 eligible patients were treated with TS1-Cisplatin at Hanoi Medical University Hospital from January 2018 to December 2021.

Results: The mean age was 57.4. The male to female ratio was 3.2:1. Most patients had good performance status (PS 0 or PS 1 - 84.2%). Most received a dose rate from 85% to 100% of the standard dose (78.9%). After six cycles, the complete response rate was 13.2%, and the partial response rate was 42.1%. The median progression-free survival was 5.7 months, and the median overall survival was 13.5 months. Neutropenia was the most common adverse event (52.6%), with 13.1% in grade 3-4. Diarrhea accounted for 36.8%, with only one case in grade 3 (2.6%). Only one patient experienced hand-foot syndrome (2.6%).

Conclusion: The TS1-Cisplatin regimen in metastatic gastric cancer demonstrated a good response rate while being safe and tolerable.

https://doi.org/10.38103/jcmhch.78.3

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Đã xuất bản 25-03-2022
Toàn văn
Ngôn ngữ
Số tạp chí Số 78 (2022)
Phân mục Nghiên cứu
DOI 10.38103/jcmhch.78.3
Từ khóa Advanced gastric cancer, TS1, cisplatin Advanced gastric cancer, TS1, cisplatin

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Bản quyền (c) 2022 Tạp chí Y học lâm sàng Bệnh viện Trung Ương Huế

Le, H. T., & Pham, D. M. (2022). Evaluating the efficacy and safety of TS1 - Cisplatin regimen in the first - line treatment of advanced gastric cancer patients. Tạp Chí Y học lâm sàng Bệnh viện Trung Ương Huế, (78), 13–17. https://doi.org/10.38103/jcmhch.78.3