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
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

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.
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…
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Taxonomy
TopicsHepatocellular Carcinoma Treatment and Prognosis · Immunotherapy and Immune Responses · Cancer Immunotherapy and Biomarkers
