# Conversion Surgery for Alpha-Fetoprotein–Producing Esophagogastric Junction Cancer with Multiple Liver Metastases and Portal Vein Tumor Thrombus after Nivolumab Combination Chemotherapy: A Case Report and Literature Review

**Authors:** Masaaki Akai, Shoji Takagi, Tomohiro Toji, Yoshifumi Mitani, Mikoto Shimabara, Yuta Nobunaga, Toshihisa Matsumura, Masafumi Inoue

PMC · DOI: 10.70352/scrj.cr.25-0808 · Surgical Case Reports · 2026-02-26

## TL;DR

A rare case of esophagogastric junction cancer with liver metastases was successfully treated with a combination of chemotherapy and surgery, leading to long-term remission.

## Contribution

This case report demonstrates the feasibility of conversion surgery after nivolumab-based chemotherapy for AFP-producing cancer with liver metastases.

## Key findings

- Combination therapy with S-1, oxaliplatin, and nivolumab led to rapid disappearance of liver metastases and normalization of AFP levels.
- Conversion surgery achieved a complete pathological response with no recurrence 12 months post-surgery.
- The treatment approach may be effective for selected patients with AFP-producing esophagogastric junction cancer.

## Abstract

Alpha-fetoprotein–producing gastric cancer (AFPGC) is a rare subtype of gastric cancer associated with poor prognosis due to early liver metastasis. There have been limited reports on conversion surgery following nivolumab combination chemotherapy in cases of AFPGC with liver metastasis. Here, we present a case of alpha-fetoprotein–producing esophagogastric junction cancer (AFP-EGJC) successfully treated with this treatment.

The patient was a 31-year-old man. After liver tumors were incidentally detected, he was diagnosed with esophagogastric junction cancer (cT3N1M1) with multiple liver metastases and portal vein tumor thrombus. Combination therapy with S-1 (tegafur/gimeracil/oteracil), oxaliplatin, and nivolumab was initiated. The response was remarkable, with the rapid disappearance of liver metastases. Serum AFP was also abnormally high at 691.9 ng/mL, but it quickly normalized after the start of treatment. Fifteen months later, the patient was diagnosed with progressive disease, and the regimen was switched to nab-paclitaxel and ramucirumab therapy. However, there was no recurrence of liver metastases, and only the primary tumor was poorly controlled. Therefore, a laparoscopic proximal gastrectomy was performed 22 months after the initial treatment. The postoperative diagnosis was ypT2 (MP) N0M0, ypStage IB. The patient remains alive and recurrence-free 12 months after surgery, without adjuvant chemotherapy.

Conversion surgery after nivolumab combination chemotherapy may be feasible in selected patients with AFP-EGJC with liver metastasis.

## Linked entities

- **Chemicals:** S-1 (PubChem CID 1497102), tegafur (PubChem CID 5386), gimeracil (PubChem CID 54679224), oteracil (PubChem CID 4604), oxaliplatin (PubChem CID 9887053), nab-paclitaxel (PubChem CID 36314)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}
- **Diseases:** AFPGC (MESH:D013274), yolk sac tumors (MESH:D018240), esophageal invasion (MESH:D004941), liver lesions (MESH:D008107), Esophagogastric junction cancer (MESH:D009369), adenocarcinoma (MESH:D000230), PRESENTATION (MESH:D001946), lymph node metastasis (MESH:D008207), IV (MESH:D006011), lymph node swelling (MESH:D000072717), vein (MESH:D000071078), liver (MESH:D017093), hepatocellular carcinoma (MESH:D006528), liver tumors (MESH:D008113), Liver Metastases (MESH:D009362), Portal Vein Tumor Thrombus (MESH:D013927), CS (MESH:D006223), Stage IV disease (MESH:D007676)
- **Chemicals:** tegafur (MESH:D005641), oxaliplatin (MESH:D000077150), ramucirumab (MESH:C543333), CS (MESH:D002586), Ram (MESH:C071315), gimeracil (MESH:C104201), eosin (MESH:D004801), Nivo (MESH:D000077594), HE (MESH:D006371), PTX (-), hematoxylin (MESH:D006416), oteracil (MESH:D010094)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946830/full.md

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Source: https://tomesphere.com/paper/PMC12946830