# Use of Chemoimmunotherapy for Locally Advanced Deficient Mismatch Repair (dMMR) Gastric Adenocarcinoma With Curative Intent: A Case Report

**Authors:** Beatriz Gonzalez Diez, Maria Jesus Fernandez Aceñero, Ramiro Jesus Mendez, Esteban Martin-Antona, Javier Sastre

PMC · DOI: 10.7759/cureus.63527 · 2024-06-30

## TL;DR

A patient with advanced gastric cancer showed a complete response to chemoimmunotherapy, suggesting it could be an effective treatment for similar cases.

## Contribution

This case report highlights chemoimmunotherapy as a potential neoadjuvant treatment for MSI-H gastric cancer.

## Key findings

- The patient achieved complete pathologic tumor response after chemoimmunotherapy.
- Radiological remission was maintained for over a year following treatment.
- The treatment allowed curative surgery in a previously unresectable case.

## Abstract

The standard of care for patients with operable gastric adenocarcinoma is perioperative chemotherapy and surgical resection. The deficient mismatch repair (dMMR)/microsatellite instability (MSI-H) phenotype is a major predictive biomarker for immune checkpoint inhibitors (ICIs) efficacy in advanced disease. Several phase II and III trials suggest a promising future role of immunotherapy with or without chemotherapy in the neoadjuvant/adjuvant setting, especially in MSI-H localized gastric adenocarcinomas. We present a 38-year-old man diagnosed in March 2022 with poorly differentiated gastric adenocarcinoma clinical stage III (cT4 N0 M0) with deficiency of MLH1 and PMS2, combined positive score (CPS) of 100 and negative HER2 immunohistochemistry, had poor tumor response to preoperative 5-FU, leucovorin, oxaliplatin, and docetaxel (FLOT). It was considered unresectable because of the involvement of the colon, mesocolon, duodenum, pancreas, and retroperitoneum. Then, first-line systemic treatment with 5-FU, leucovorin, and oxaliplatin (FOLFOX)-nivolumab was initiated in August 2022, with a significant radiologic tumor reduction after six cycles, allowing a curative surgery in March 2023 with complete pathologic tumor response, followed by capecitabine and nivolumab for one year, maintaining radiological remission in the last follow-up in April 2024. With this case report, we conclude that it is likely that chemoimmunotherapy or immunotherapy alone may be alternative neoadjuvant treatment choices for MSI-H locally advanced gastric cancer patients.

## Linked entities

- **Genes:** MLH1 (mutL homolog 1) [NCBI Gene 4292], PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064]
- **Chemicals:** 5-FU (PubChem CID 3385), leucovorin (PubChem CID 135403648), oxaliplatin (PubChem CID 9887053), docetaxel (PubChem CID 148124), capecitabine (PubChem CID 60953)
- **Diseases:** gastric adenocarcinoma (MONDO:0005036)

## Full-text entities

- **Genes:** PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395] {aka HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMSL2}, MLH1 (mutL homolog 1) [NCBI Gene 4292] {aka COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** tumor (MESH:D009369), Gastric Adenocarcinoma (MESH:D013274)
- **Chemicals:** 5-FU, leucovorin, and oxaliplatin (-), 5-FU (MESH:D005472), FOLFOX (MESH:C410216), capecitabine (MESH:D000069287), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11288636/full.md

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Source: https://tomesphere.com/paper/PMC11288636