# Case Report: Complete response to four cycles of camrelizumab in a PD-L1 negative patient with advanced oral squamous cancer

**Authors:** Jianqiao He, Guoning Yu, Yi Ma, Xiaoqiong Shi, Yingna Gao, Hongliang Zheng, Minhui Zhu, Caiyun Zhang

PMC · DOI: 10.3389/fimmu.2025.1476455 · Frontiers in Immunology · 2025-02-24

## TL;DR

A patient with advanced oral cancer achieved complete recovery after four cycles of immunotherapy, despite lacking a key biomarker typically used to predict treatment success.

## Contribution

This case report highlights an unexpected complete response to short-term immunotherapy in a PD-L1 negative patient, suggesting new biomarkers may exist.

## Key findings

- A PD-L1 negative patient achieved complete response after four cycles of camrelizumab.
- TP53/FANCA/FAT1 gene mutations were identified in the patient's tumor.
- The patient remained disease-free for four years without recurrence or metastasis.

## Abstract

Immunotherapy has brought better survival benefits in the treatment of recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC). However, owing to the lack of relevant biomarkers that could predict the efficacy of this treatment, it often has to be maintained. Here we report on a patient with stage IVA squamous cell carcinoma of the tongue who developed an unresectable lesion in the neck after surgery and radical chemoradiotherapy. After four cycles of intermittent immunotherapy with camrelizumab, complete response (CR) was achieved. Next-generation sequencing showed that the TP53/FANCA/FAT1 gene mutations and negative PD-L1 expression were involved. The patient has been followed up for 4 years without R/M. This situation has not been reported previously, suggesting that some patients can benefit from short-term immunotherapy and even achieve CR; moreover, there may be more molecular markers to be discovered that can predict the efficacy of immunotherapy. We can conduct in-depth research on relevant molecular markers, formulate personalized immunotherapy strategies and plans, and facilitate the development of new precision treatment strategies for HNSCC.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], FANCA (FA complementation group A) [NCBI Gene 2175], FAT1 (FAT atypical cadherin 1) [NCBI Gene 2195]
- **Diseases:** oral squamous cell carcinoma (MONDO:0004958), head and neck squamous cell carcinoma (MONDO:0010150)

## Full-text entities

- **Genes:** FAT1 (FAT atypical cadherin 1) [NCBI Gene 2195] {aka CDHF7, CDHR8, FAT, ME5, hFat1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, FANCA (FA complementation group A) [NCBI Gene 2175] {aka FA, FA-H, FA1, FAA, FACA, FAH}
- **Diseases:** oral squamous cancer (MESH:D018307), HNSCC (MESH:D000077195), IVA (MESH:C538167)
- **Chemicals:** camrelizumab (MESH:C000631724)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11891172/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC11891172/full.md

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Source: https://tomesphere.com/paper/PMC11891172