# Case Report: Pathological complete response achieved with neoadjuvant immunochemotherapy in synchronous multiple gastric adenocarcinoma

**Authors:** Ya-hui Sun, Yan Ma, Liang Chen, Hai-rong Li, Xian-Wen Liang, Xiong-hui He, Ke-jian Zou

PMC · DOI: 10.3389/fimmu.2025.1611281 · Frontiers in Immunology · 2025-07-18

## TL;DR

A rare case of multiple stomach cancers showed complete response to immunochemotherapy, suggesting immunotherapy could be effective in treating this condition.

## Contribution

First documented case of synchronous multiple gastric cancer achieving pathological complete response with neoadjuvant immunochemotherapy.

## Key findings

- Patient with advanced gastric cancer achieved partial response after three cycles of neoadjuvant immunochemotherapy.
- Histopathological analysis confirmed pathological complete response following surgery.
- Immunotherapy combined with chemotherapy may convert unresectable gastric cancer to resectable disease.

## Abstract

Synchronous multiple gastric cancers (SMGC) represent a rare clinical entity with no established treatment guidelines. We report a 76-year-old female with two synchronous poorly differentiated adenocarcinomas (dMMR/MSI-H phenotype) in the gastric lesser curvature, clinically staged as cT4bN2M0. Following three cycles of neoadjuvant immunochemotherapy, the patient demonstrated remarkable tumor regression (RECIST 1.1 partial response) and subsequently underwent R0 distal gastrectomy. Histopathological examination confirmed a pathological complete response (ypT0N0, TRG 0).To our knowledge, this represents the first documented case of SMGC achieving pCR with neoadjuvant immunochemotherapy. Our findings suggest that PD-1 inhibition combined with chemotherapy may induce profound tumor regression in SMGC, even in cases with high tumor burden, potentially converting unresectable to resectable disease. This case provides compelling evidence for incorporating immunotherapy in SMGC management and warrants further investigation through clinical trials.

## Linked entities

- **Diseases:** gastric adenocarcinoma (MONDO:0005036), adenocarcinoma (MONDO:0004970)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** tumor (MESH:D009369), adenocarcinomas (MESH:D000230), poorly differentiated (MESH:D020522), MSI-H (MESH:D000848), SMGC (MESH:D013274)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12313488/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12313488/full.md

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Source: https://tomesphere.com/paper/PMC12313488