Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, Japan.
Department of Gastroenterological Surgery, Cancer Institute Hospital of JFCR, Tokyo, Japan.
Sci Rep. 2024 Sep 19;14(1):21854. doi: 10.1038/s41598-024-72423-x.
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.
本研究旨在调查真实世界环境中化疗方案的疗效,并探索早期复发的胃癌患者最有前途的治疗方案。我们回顾性分析了 2012 年至 2016 年期间,19 家日本机构的 207 例接受 S-1 辅助治疗后发生早期复发(复发发生在完成辅助治疗期间或 6 个月内)的胃癌患者的临床病程。复发后的治疗方案包括:氟嘧啶加铂类方案(FP)91 例(44%),紫杉醇类方案(PTX)102 例(49%),伊立替康类方案(IRI)14 例(7%)。总缓解率和疾病控制率分别为 28.7%和 54.1%。中位无进展生存期(PFS)和总生存期(OS)分别为 5.1 和 12.9 个月。在 FP、PTX 和 IRI 方案中,中位 PFS 和 OS 分别为 5.9、4.1、4.1 个月和 12.8、12.9 和 11.8 个月。PTX 联合雷莫芦单抗的疗效与卡培他滨加铂类相当。OS 的多因素分析显示,辅助化疗期间复发和未分化组织学类型是独立的不良预后因素。尽管接受辅助 S-1 治疗后早期复发患者的预后较差,但 PTX 联合雷莫芦单抗治疗可能是一种潜在的治疗选择。