# SOX combined with apatinib and camrelizumab in the treatment of resectable locally advanced gastric cancer: a case report

**Authors:** JiKe Hu, Xuemei Li, Yunpeng Wang, Bo Xu, Puyi He, Zhuanfang Wang, Lijuan He, Hao Chen

PMC · DOI: 10.3389/fimmu.2024.1410284 · Frontiers in Immunology · 2024-07-12

## TL;DR

A patient with advanced gastric cancer was successfully treated with a combination of SOX, apatinib, and camrelizumab before and after surgery, showing promising results.

## Contribution

This case report demonstrates the potential efficacy of combining SOX, apatinib, and camrelizumab in treating resectable locally advanced gastric cancer.

## Key findings

- The patient achieved a pathological complete response after neoadjuvant therapy with SOX, apatinib, and camrelizumab.
- Postoperative follow-up showed no recurrence or metastasis during adjuvant therapy.
- The treatment was well-tolerated with manageable side effects.

## Abstract

Gastric cancer is highly prevalent in China, yet early diagnosis and overall survival rates are low. The primary treatment strategy is comprehensive therapy centered on surgery. Studies indicate that neoadjuvant chemotherapy can enhance radical resection rates and extend survival in locally advanced gastric cancer. Combining VEGFR inhibitors with chemotherapy improves efficacy in digestive system tumors, while PD-1/PD-L1 inhibitors combined with anti-angiogenesis agents or chemotherapy show synergistic effects. This report presents a case of gastric adenocarcinoma (cT3N1M0) treated with SOX, apatinib mesylate, and camrelizumab as neoadjuvant therapy, followed by D2 distal gastrectomy and postoperative adjuvant therapy with the same regimen. The patient completed all treatment cycles successfully. Post-neoadjuvant therapy, only focal residual cancer cells were found in the lamina propria (pT1a). During postoperative adjuvant therapy follow-up, gastroscopic biopsy indicated a pathological complete response with no recurrence or metastasis. The patient primarily experienced dyspepsia, oropharyngeal pain, capillary proliferation, mild bone marrow suppression, nausea, and vomiting as side effects. Therefore, SOX combined with apatinib mesylate and camrelizumab shows promise for treating resectable locally advanced gastric cancer.

## Linked entities

- **Chemicals:** apatinib mesylate (PubChem CID 45139106)
- **Diseases:** gastric cancer (MONDO:0001056), gastric adenocarcinoma (MONDO:0005036)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** oropharyngeal pain (MESH:D009959), cancer (MESH:D009369), vomiting (MESH:D014839), nausea (MESH:D009325), bone marrow suppression (MESH:D001855), metastasis (MESH:D009362), Gastric cancer (MESH:D013274), dyspepsia (MESH:D004415)
- **Chemicals:** camrelizumab (MESH:C000631724), SOX (-), apatinib (MESH:C553458)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11272450/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC11272450/full.md

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Source: https://tomesphere.com/paper/PMC11272450