Efficacy of chemotherapy for patients with gastric cancer with early recurrence during or after adjuvant chemotherapy with S-1 alone: a multicenter retrospective study
- PMID: 39300169
- PMCID: PMC11413207
- DOI: 10.1038/s41598-024-72423-x
Efficacy of chemotherapy for patients with gastric cancer with early recurrence during or after adjuvant chemotherapy with S-1 alone: a multicenter retrospective study
Abstract
This study aimed to survey the efficacy of chemotherapy regimens in the real world setting and explore the most promising regimen for patients experiencing early recurrence for gastric cancer. We retrospectively reviewed the clinical course of 207 patients with gastric cancer, who developed early recurrence during or within 6 months after completing S-1 adjuvant therapy at 19 Japanese institutions between 2012 and 2016. The treatment regimens after recurrence were fluoropyrimidines plus platinum-based regimens (FP) in 91 (44%) patients, paclitaxel-based regimens (PTX) in 102 (49%), and irinotecan-based regimens (IRI) in 14 (7%). The overall response and disease control rates were 28.7% and 54.1%. Median progression-free survival (PFS) and overall survival (OS) were 5.1 and 12.9 months, respectively. In the FP, PTX, and IRI regimens, the median PFS and OS were 5.9, 4.1, 4.1 months and 12.8, 12.9, and 11.8 months, respectively. The combination of PTX and ramucirumab showed survival comparable to capecitabine plus platinum. Multivariate analyses for OS showed that recurrence during adjuvant chemotherapy and undifferentiated histological type were independent poor prognostic factors. Although the prognosis of patients with early recurrence even with adjuvant S-1 was poor, PTX plus ramucirumab therapy could be a potential treatment option.
Keywords: Early relapse; Gastric cancer; Paclitaxel; Ramucirumab; S-1.
© 2024. The Author(s).
Conflict of interest statement
Dr. Kengo Nagashima reports consulting fees from SENJU Pharmaceutical Co., Ltd, Toray Industries, Inc., and Kowa Company, Ltd, outside the submitted work. Dr. Takanobu Yamada reports personal fees from Taiho, Ono pharmaceutical, Bristol Squib Mayers, and Johnson and Johnson, outside the submitted work. Dr. Haruhiko Cho reports personal fees from Yakult Honsha, outside the submitted work. Dr. Shigenori Kadowaki reports personal fees from MSD, Merck KgaA, Eli Lilly, Bayer, Daiichi Sankyo, Eisai, Taiho, Ono pharmaceutical, Bristol Squib Mayers, and Chugai Pharmaceutical, outside the submitted work. Dr. Narikazu Boku reports personal fees from Taiho and Ono, Eli Lilly, Taiho, Daiichi Sankyo, and Bristol-Myers Squibb, outside the submitted work. All remaining authors have declared no conflicts of interest.
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