# Case Report: Long-term disease-free survival in an advanced hepatocellular carcinoma patient: an exceptional response to PD-1 inhibitor therapy

**Authors:** Qinliang Fang, Shuqi Yu, Yu Xiong, Yibin Zhang, Xiaomin Wang, Jianyin Zhou, Fuqiang Wang, Zhenyu Yin

PMC · DOI: 10.3389/fimmu.2025.1677724 · Frontiers in Immunology · 2025-11-11

## TL;DR

A patient with advanced liver cancer achieved long-term remission using a reduced dose of a PD-1 inhibitor, offering hope for similar treatments.

## Contribution

Demonstrates exceptional long-term disease-free survival with reduced-dose PD-1 inhibitor in advanced HCC.

## Key findings

- A 55-year-old male achieved complete remission after four cycles of reduced-dose pembrolizumab.
- The patient remained disease-free for over seven years, highlighting the potential of personalized dosing.
- The case provides insights into managing immune-related adverse events with PD-1 inhibitors.

## Abstract

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death, with most patients diagnosed at advanced stages, often precluding surgical resection. Recently, immune checkpoint inhibitors, particularly PD-1 inhibitors, have emerged as promising therapies, though long-term disease-free survival (DFS) remains rare. We report a case of an advanced HCC patient who achieved complete remission (CR) after just four cycles of reduced-dose pembrolizumab and maintained a disease-free status for more than seven years.

A 55-year-old male with chronic hepatitis B and alcohol-related liver disease presented with a ruptured HCC. After initial treatments, including surgery and chemotherapy, the patient was started on reduced-dose pembrolizumab (100 mg). After four cycles, the patient achieved CR.

This case highlights the potential for long-term survival with reduced-dose PD-1 inhibitor therapy in advanced HCC. The patient’s exceptional response provides important insights into the role of personalized dosing, immune checkpoint inhibitors, and the management of immune-related adverse events.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), chronic hepatitis B (MONDO:0005344)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** cancer (MESH:D009369), death (MESH:D003643), HCC (MESH:D006528), chronic hepatitis B (MESH:D019694), alcohol-related liver disease (MESH:D008108)
- **Chemicals:** pembrolizumab (MESH:C582435)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12643963/full.md

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Source: https://tomesphere.com/paper/PMC12643963