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Survival Outcomes and Clinicopathologic Prognostic Factors in Gastric Cancer: A Small Single-Center Retrospective Cohort From Eastern Türkiye.

Cureus 2026 Vol.18(1) p. e101204

Gökçen S, Yerlikaya MB, Aslan A, Bayram H, Tüfekçi T, Verendag YO

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[INTRODUCTION] Real-world data from eastern Türkiye regarding gastric cancer outcomes remain limited.

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APA Gökçen S, Yerlikaya MB, et al. (2026). Survival Outcomes and Clinicopathologic Prognostic Factors in Gastric Cancer: A Small Single-Center Retrospective Cohort From Eastern Türkiye.. Cureus, 18(1), e101204. https://doi.org/10.7759/cureus.101204
MLA Gökçen S, et al.. "Survival Outcomes and Clinicopathologic Prognostic Factors in Gastric Cancer: A Small Single-Center Retrospective Cohort From Eastern Türkiye.." Cureus, vol. 18, no. 1, 2026, pp. e101204.
PMID 41669603

Abstract

[INTRODUCTION] Real-world data from eastern Türkiye regarding gastric cancer outcomes remain limited. We aimed to describe overall survival (OS) and explore associations between OS and key clinicopathologic factors in a small, single-center cohort.

[METHODS] We retrospectively reviewed consecutive adults with gastric adenocarcinoma who underwent gastrectomy with curative intent between January 2019 and June 2025. Perioperative mortality (<30 days) was excluded to focus on long-term oncologic outcomes. OS was defined from surgery to death from any cause; survivors were administratively censored at June 2, 2025. Kaplan-Meier methods and univariate Cox models were used.

[RESULTS] Thirty patients were included (mean age 65.8±9.4 years; 20/30 male). Median follow-up among survivors was 19.2 months (IQR 8.2-30.8). Twelve- and 24-month OS were 71.1% and 62.2%, respectively; median OS was not reached. Median retrieved lymph nodes was 20 (IQR 19-36; range 4-61). Median lymph node ratio (LNR) was 0.09 (IQR 0.04-0.21). Older age showed a borderline association with worse OS in univariate Cox analysis.

[CONCLUSIONS] In this small exploratory cohort, OS estimates were modest and associations with clinicopathologic variables were largely inconclusive due to limited power. Larger, multicenter cohorts with standardized reporting of histology, staging, and perioperative treatment are required.