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Survival impact of microsatellite instability in stage II gastric cancer patients who received S-1 adjuvant monotherapy after curative resection.
Sato, Chihiro; Kawakami, Hisato; Tanaka, Ryo; Satake, Hironaga; Inoue, Kentaro; Kimura, Yutaka; Fujita, Junya; Kawabata, Ryohei; Chiba, Yasutaka; Satoh, Taroh; Nakagawa, Kazuhiko.
Affiliation
  • Sato C; Department of Medical Oncology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Japan.
  • Kawakami H; Laboratory of Molecular Immunology, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo, Japan.
  • Tanaka R; Department of Medical Oncology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Japan. kawakami_h@med.kindai.ac.jp.
  • Satake H; Department of General and Gastrointestinal Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
  • Inoue K; Cancer Center, Kansai Medical University Hospital, Hirakata, Japan.
  • Kimura Y; Department of Medical Oncology, Kochi Medical School, Kochi, Japan.
  • Fujita J; Department of Surgery, Kansai Medical University Hospital, Hirakata, Japan.
  • Kawabata R; Department of Surgery, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.
  • Chiba Y; Department of Surgery, Kindai University Nara Hospital, Ikoma, Japan.
  • Satoh T; Department of Surgery, Yao Municipal Hospital, Yao, Japan.
  • Nakagawa K; Department of Surgery, Sakai City Medical Center, Sakai, Japan.
Sci Rep ; 13(1): 10826, 2023 07 04.
Article in En | MEDLINE | ID: mdl-37402831
ABSTRACT
Adjuvant S-1 monotherapy is the standard of care for stage II gastric cancer (GC) after curative resection in Japan, but its efficacy for microsatellite instability-high (MSI-H) tumors has remained unknown. Among a multi-institutional cohort of patients with stage II GC who underwent R0 resection followed by S-1 adjuvant chemotherapy between February 2008 and December 2018, we assessed MSI status with an MSI-IVD Kit (Falco). MSI status was assessable for 184 (88.5%) of the 208 enrolled patients, with MSI-H being identified in 24 (13.0%) individuals. Although neither relapse-free survival (RFS) (hazard ratio [HR] = 1.00, p = 0.997) nor overall survival (OS) (HR = 0.66, p = 0.488) differed between MSI-H versus microsatellite-stable (MSS) patients, MSI-H patients showed a nonsignificant but better RFS (HR = 0.34, p = 0.064) and OS (HR = 0.22, p = 0.057) than did MSS patients after adjustment for background characteristics by propensity score (PS) analysis. Gene expression analysis in the PS-matched cohort suggested that recurrence was associated with the immunosuppressive microenvironment in MSI-H tumors but with expression of cancer/testis antigen genes in MSS tumors. Our data reveal a better adjusted survival for MSI-H versus MSS stage II GC treated with S-1 adjuvant therapy, and they suggest that mechanisms of recurrence differ between MSI-H and MSS tumors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Sci Rep Year: 2023 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Sci Rep Year: 2023 Document type: Article Affiliation country: Japón