Real-world outcomes of trifluridine/tipiracil for heavily pretreated patients with advanced gastric cancer

Autor: 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
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: ESMO Gastrointestinal Oncology, Vol 3, Iss , Pp 100046- (2024)
Druh dokumentu: article
ISSN: 2949-8198
DOI: 10.1016/j.esmogo.2024.100046
Popis: 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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