# Case Report: A neoantigen-targeting peptide vaccine combined with checkpoint inhibition induces tumor regression and long-term remission in a pediatric patient with metastatic hepatocellular carcinoma

**Authors:** Germano Amorelli, Armin Rabsteyn, Claus-Philipp Maier, Finn Trautner, Ursula Holzer, Jürgen Frank Schäfer, Martin Ebinger, Rupert Handgretinger, Sven Nahnsen, Hans-Georg Rammensee, Peter Lang

PMC · DOI: 10.3389/fimmu.2025.1674663 · 2025-10-31

## TL;DR

A personalized vaccine combined with checkpoint inhibition led to complete tumor regression and long-term remission in a child with aggressive liver cancer.

## Contribution

Demonstration of durable remission in pediatric metastatic HCC using neoantigen-targeting vaccine and checkpoint inhibition.

## Key findings

- Complete regression of inoperable metastasis following neoantigen vaccine and checkpoint inhibition.
- Robust and neoepitope-specific T-cell responses confirmed via immunomonitoring and TCR sequencing.
- Patient remained in complete remission for 13 years, exceeding prior survival outcomes in similar therapies.

## Abstract

Pediatric hepatocellular carcinoma (HCC) is a rare and aggressive malignancy with limited treatment options and poor prognosis, highlighting the need for innovative therapeutic strategies. Neoantigen-targeting peptide vaccination is a promising treatment approach with potential for combination therapy with checkpoint inhibition (CPI). Here, we present a case study of a pediatric patient with metastatic HCC treated with a neoantigen-derived peptide vaccine combined with CPI therapy after disease recurrence. Immunomonitoring revealed robust vaccine-induced T-cell responses, further enhanced by CPI. T-cell cloning and T-cell receptor (TCR) sequencing confirmed neoepitope specificity and clonality of the vaccine-induced T-cell response. Following immunotherapy, the inoperable metastasis regressed completely, with no further intervention. A subsequent metastasis was surgically resected, and the patient has remained in complete remission since, with an overall survival (OS) of 13 years. These findings underscore the potential of personalized peptide vaccination and demonstrate the feasibility and efficacy of combinatorial strategies in optimizing therapeutic outcome in pediatric HCC. Importantly, this case illustrates a uniquely durable remission in pediatric metastatic HCC, exceeding survival outcomes reported in previous vaccine or CPI monotherapy studies.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}
- **Diseases:** malignancy (MESH:D009369), metastasis (MESH:D009362), HCC (MESH:D006528)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615373/full.md

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Source: https://tomesphere.com/paper/PMC12615373