Authors
Sait Kitapli, Ali Alkan, Ozgur Tanriverdi
Published in
Helicobacter. Volume 31. Issue 4. Pages e70150.
Abstract
The prognostic significance of Helicobacter pylori (H. pylori) infection in metastatic colorectal cancer (mCRC) remains uncertain. Most prior studies have focused on colorectal neoplasia risk and have relied on serological markers rather than assessment of active infection. We evaluated the association between histologically confirmed H. pylori status and clinicopathological features, systemic inflammatory markers, and survival outcomes in patients with de novo mCRC.
In this retrospective single-center cohort study, consecutive patients diagnosed with de novo mCRC between September 2011 and December 2025 who underwent synchronous upper gastrointestinal endoscopy at diagnosis were included. H. pylori status was determined histopathologically. Overall survival (OS) was estimated using the Kaplan-Meier method and compared with the log-rank test. Prognostic factors were analyzed using univariable and multivariable Cox proportional hazards models with prespecified sensitivity and exploratory interaction analyses.
Among 168 patients, 77 (46%) were H. pylori positive. Right-sided tumors were more frequent in H. pylori-positive patients (43% vs. 17%, p < 0.001), as was BRAF mutation (12% vs. 3%, p = 0.044). Baseline neutrophil-to-lymphocyte ratio was higher in the H. pylori-positive group (median 4.34 vs. 2.74, p = 0.002). Median OS was longer in H. pylori-positive patients (33 vs. 19 months; log-rank p < 0.001). In multivariable analysis, right-sided tumor localization (HR 2.11, 95% CI: 1.648-2.716; p < 0.001), RAS mutation (HR 1.94, 95% CI: 1.612-2.794; p < 0.001), and H. pylori negativity (HR 1.94, 95% CI: 1.569-2.812; p < 0.001) remained statistically significant. These findings were consistent across sensitivity analyses. Significant interactions were observed for tumor sidedness (p < 0.001) and NLR category (p = 0.002).
Histologically confirmed H. pylori positivity was associated with a distinct clinicopathological profile and longer overall survival in patients with de novo mCRC. Given the observational design, these findings should be interpreted as hypothesis-generating and require validation in prospective and multi-center studies.
PMID:
42410912
Bibliographic data and abstract were imported from PubMed on 07 Jul 2026.
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