三氟啶/替比拉嘧啶治疗重度预处理晚期胃癌患者的实际效果

K. Fukuda , I. Nakayama , A. Ooki , D. Kamiimabeppu , K. Shimozaki , H. Osumi , S. Fukuoka , K. Yoshino , M. Ogura , T. Wakatsuki , K. Chin , E. Shinozaki , K. Yamaguchi , D. Takahari
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引用次数: 0

摘要

背景三氟尿苷(FTD)/替吡咯(TPI)是晚期胃癌(AGC)的标准挽救治疗方法。材料与方法这项回顾性队列研究于2019年11月至2022年5月在日本一家研究所进行,纳入了无法手术的晚期或复发性胃癌(GC)患者,这些患者在三线或三线以上接受了FTD/TPI联合或不联合拉莫单抗(RAM)治疗。研究人员对这些患者进行了单变量和多变量分析,以研究与疾病进展和生存期相关的临床因素。85名患者在接受FTD/TPI治疗前曾使用过免疫检查点抑制剂,86名患者接受了FTD/FPI作为第四线或更后一线治疗。客观反应率为2.3%(2/87),疾病控制率为40.2%(35/87)。恶心、厌食和腹泻分别在45、24和19例患者中出现。最常见的3级或4级不良反应是中性粒细胞减少。多变量分析显示,表现状态(PS)≥1、血清癌胚抗原(CEA)和/或碳水化合物抗原19-9(CA19-9)水平升高以及原发肿瘤位置与较短的无进展生存期独立相关。在总生存期方面,PS≥1、血清癌胚抗原(CEA)和/或CA19-9升高以及出现中度至重度腹水与较差的生存期有统计学意义。与FTD/TPI相关的AEs在重度预处理的AGC患者中是可控的。
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Real-world outcomes of trifluridine/tipiracil for heavily pretreated patients with advanced gastric cancer

Background

Trifluridine (FTD)/tipiracil (TPI) is a standard salvage treatment for advanced gastric cancer (AGC). This study aimed to assess the efficacy and safety of FTD/TPI in heavily pretreated patients with AGC in clinical practice.

Materials and methods

This retrospective cohort study conducted at a single Japanese institute between November 2019 and May 2022 included patients with inoperable advanced or recurrent gastric cancer (GC) who received FTD/TPI with or without ramucirumab (RAM) in the third-line or later setting. Univariate and multivariate analyses were carried out to examine the clinical factors associated with disease progression and survival.

Results

A total of 98 consecutive patients, including 2 patients treated with RAM, were enrolled. Eighty-five patients had prior immune checkpoint inhibitor administration before FTD/TPI and 86 patients were treated with FTD/FPI as the fourth or later line of treatment. Objective response rate was 2.3% (2/87), and disease control rate was 40.2% (35/87). Nausea, anorexia, and diarrhea were the observed adverse events (AEs) in 45, 24, and 19 patients, respectively. The most common grade 3 or 4 AE was neutropenia. Multivariate analysis revealed that performance status (PS) ≥1, elevated serum carcinoembryonic antigen (CEA) and/or carbohydrate antigen 19-9 (CA19-9) levels, and primary tumor location were independently associated with shorter progression-free survival. In terms of overall survival, PS ≥1, elevated serum CEA and/or CA19-9, and the presence of moderate to severe ascites demonstrated statistically significant associations with poorer survival.

Conclusions

FTD/TPI could be a therapeutic option for AGC patients previously treated with nivolumab in clinical practice. AEs associated with FTD/TPI were manageable in heavily pretreated patients with AGC.

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