# Dynamic variation in a combined inflammation–tumor marker index during neoadjuvant chemotherapy and its value for organ-preservation decisions in gastric cancer

**Authors:** Ke Liu, Haiquan Qian, Shensi Chen, Shengjun Zhang, Wei Zhao

PMC · DOI: 10.1515/biol-2025-1238 · Open Life Sciences · 2026-01-23

## TL;DR

A new index tracking changes during chemotherapy helps predict treatment response and supports decisions to preserve organs in gastric cancer patients.

## Contribution

A dynamic inflammation–tumor marker index (ΔCITI) is proposed as a novel biomarker for assessing neoadjuvant chemotherapy response in gastric cancer.

## Key findings

- A ≥1-point decline in ΔCITI was observed in 53.1% of patients during neoadjuvant chemotherapy.
- Favorable ΔCITI was associated with higher pathologic complete response and improved overall survival.
- ΔCITI complements imaging and biopsy for assessing treatment response and guiding organ preservation decisions.

## Abstract

We evaluated whether on-treatment change in a Combined Inflammation–Tumor Marker Index (ΔCITI) signals chemosensitivity during neoadjuvant chemotherapy (NAC) for gastric cancer and can support selective organ preservation. Of 179 patients, 158 (88.3 %) completed planned NAC, 164 (91.6 %) underwent resection, with pathology evaluable in 163. A ≥ 1-point ΔCITI decline occurred in 53.1 % (95/179) as cohort means fell from 4.3 to 3.2. Among resected patients (evaluable n = 163), favorable ΔCITI was associated with higher pCR (22.5 % vs 9.8 %), R0 resection was achieved in 148/163 (90.8 %). In multivariable Cox models adjusting for regimen (FLOT vs SOX), baseline CITI, and clinicopathologic factors, favorable ΔCITI predicted improved overall survival (adjusted HR 0.62, 95 % CI 0.43–0.91) and showed a directionally favorable disease-free survival (adjusted HR 0.76, 95 % CI 0.55–1.06). A multidisciplinary pathway identified 15/179 (8.4 %) candidates for organ preservation, 11 proceeded, and 2/11 (18.2 %) experienced local regrowth, both salvaged. Given the small size and limited follow-up of this subgroup, these findings are exploratory. ΔCITI ≥ 1 offers a simple, dynamic indicator that complements imaging and endoscopy/biopsy for NAC response assessment and cautious MDT-guided de-escalation. Prospective validation and head-to-head comparisons with established indices are warranted.

## Linked entities

- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}
- **Diseases:** nausea/vomiting (MESH:D020250), peripheral neuropathy (MESH:D010523), gastrointestinal (GI) malignancies (MESH:D005770), esophageal cancer (MESH:D004938), metastases (MESH:D009362), colorectal and gastric cancers (MESH:D015179), neutropenia (MESH:D009503), hematologic adverse events (MESH:D064420), nodal (MESH:D013611), bleeding (MESH:D006470), LAGC (MESH:D013274), T3 disease (MESH:C537047), -node involvement (MESH:D012804), NLR (MESH:D015467), fibrosis (MESH:D005355), Inflammation (MESH:D007249), Tumors (MESH:D009369), peritoneal carcinomatosis (MESH:D010534), esophageal and rectal cancers (MESH:D012004)
- **Chemicals:** creatinine (MESH:D003404), docetaxel (MESH:D000077143), 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel (-), ECF (MESH:C080222), 5-FU (MESH:D005472), leucovorin (MESH:D002955), oxaliplatin (MESH:D000077150), bilirubin (MESH:D001663)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917559/full.md

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Source: https://tomesphere.com/paper/PMC12917559