Published online Oct 15, 2026. doi: 10.4251/wjgo.122796
Revised: June 11, 2026
Accepted: June 30, 2026
Published online: October 15, 2026
Processing time: 142 Days and 17.5 Hours
Neoadjuvant immunotherapy with chemotherapy (NICT) is a relatively advanced treatment modality for locally advanced gastric cancer (LAGC). However, reliable peripheral blood biomarkers for predicting the efficacy and prognosis of this therapy remain lacking. We aimed to investigate and evaluate whether baseline and post-treatment changes in peripheral blood inflammatory markers and T lymphocyte subsets could serve as potential predictive and prognostic indicators for patients with LAGC receiving NICT.
To investigate the association between changes in peripheral blood markers, treatment response, and prognosis in patients with LAGC.
We conducted a retrospective analysis of clinical data from 39 patients with LAGC who received neoadjuvant therapy with sintilimab and XELOX chemo
Multivariate analysis revealed that low-adhesion gastric cancer (non-poorly vs poorly cohesive gastric adenocarcinoma) (odds ratio = 8.522, P = 0.036) and a higher post-treatment monocyte-to-lymphocyte ratio (MLR) (odds ratio = 2.479, P = 0.035) were associated with a favorable response to treatment. A higher relative change rate in CD8+ T lymphocytes (hazard ratio = 0.970, P = 0.024) and diffuse gastric cancer (hazard ratio = 5.545, P = 0.011) may be potential prognostic factors for progression-free survival. The lymphocyte count (significant decrease from 1.44 × 109/L to 1.18 × 109/L, P < 0.001) and the platelet-to-lymphocyte ratio showed significant decreases. By contrast, the monocyte count, CD3+ and CD8+ T-cell counts, and MLR all showed significant increases (all P < 0.005).
Post-treatment MLR and relative change in CD8+ T-cell proportion are potential prognostic biomarkers for patients with LAGC receiving NICT, whereas diffuse-type gastric cancer may be related to poor prognosis.
Core Tip: This study investigated the changes in peripheral blood inflammatory markers and T-cell subsets in patients with gastric cancer at baseline and after neoadjuvant chemotherapy with sintilimab combined with XELOX. Results indicate that high post-treatment monocyte-to-lymphocyte ratio levels are associated with a favorable treatment response, a greater relative change in the proportion of CD8+ T cells may be associated with better prognosis, and diffuse-type gastric cancer may be associated with poorer clinical outcomes. These easily detectable biomarkers offer a new perspective for predicting treatment response and assessing prognosis; however, further validation is required.