# Long-term remission of microsatellite instability-high adenosquamous carcinoma in gastric antrum: a case report

**Authors:** Peng Zhang, Jing Yang, Yongyong Liu, Qing Zhou, Caiqiang Xue, Bin Zhang, Yumin Li

PMC · DOI: 10.3389/fonc.2025.1516966 · 2025-04-11

## TL;DR

A rare case of gastric adenosquamous carcinoma showed long-term remission after combined surgery, chemotherapy, and immunotherapy.

## Contribution

Demonstrates successful treatment of a rare MSI-H gastric ASC case using PD-1 inhibitors and chemotherapy.

## Key findings

- The patient achieved long-term remission after surgery and combined oxaliplatin and PD-1 inhibitor therapy.
- MSI-H and elevated PD-L1 expression were associated with treatment response in gastric adenosquamous carcinoma.
- Comprehensive molecular profiling guided personalized treatment for this rare malignancy.

## Abstract

Gastric adenosquamous carcinoma (ASC) is an exceedingly rare neoplasm. Its infrequent occurrence has resulted in sparse literature on its diagnosis and management, presenting considerable challenges for clinical practice.

A 70-year-old male presented with epigastric pain and, upon gastroscopy and CT imaging, was found to have a mass in the gastric antrum. Histopathological analysis confirmed the diagnosis of adenosquamous carcinoma. Immunohistochemical staining revealed a loss of PMS2 and MLH-1 expression, while molecular analysis confirmed MLH-1 methylation, suggesting a microsatellite instability-high (MSI-H) phenotype. The PD-L1 combined positive score (CPS) was remarkably elevated at 80. Postoperatively, the patient received six cycles of oxaliplatin in conjunction with PD-1 inhibitor therapy. At the one-year follow-up, the patient remained in long-term remission, with no evidence of recurrence.

This case underscores the potential efficacy of integrating surgery, chemotherapy, and immunotherapy in managing gastric ASC, particularly in the context of MSI-H and elevated PD-L1 expression. It further emphasizes the critical role of comprehensive molecular profiling in guiding personalized therapeutic strategies for such rare malignancies. Further research and additional case reports are imperative to establish optimal management protocols for gastric ASC and to enhance long-term outcomes.

## Linked entities

- **Genes:** PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395], MLH1 (mutL homolog 1) [NCBI Gene 4292]
- **Proteins:** CD274 (CD274 molecule)
- **Chemicals:** oxaliplatin (PubChem CID 9887053)
- **Diseases:** adenosquamous carcinoma (MONDO:0006074)

## Full-text entities

- **Genes:** MLH1 (mutL homolog 1) [NCBI Gene 4292] {aka COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395] {aka HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMSL2}
- **Diseases:** ASC (MESH:D018196), malignancies (MESH:D009369), epigastric pain (MESH:D010146)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12021638/full.md

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Source: https://tomesphere.com/paper/PMC12021638