The Treatment of Oral Squamous Cell Carcinoma with PD-1/PD-L1 Inhibitors
DOI:
https://doi.org/10.61173/2s7j6h84Keywords:
Oral squamous cell carcinoma, PD-1/PD-L1 inhibitor, immunotherapyAbstract
Oral squamous cell carcinoma (OSCC) often presents insidiously and has a high proportion of late-stage diagnosis, with a five-year survival rate of only 50% to 60% for traditional combined treatment, indicating a poor overall prognosis. Immunotherapy has now become a hotspot in tumor research, yet there are still many research shortcomings in the immunotherapy of OSCC. This article reviews the application of PD-1/PD-L1 inhibitors in OSCC. The results show that this target is highly expressed in cancer tissues, promoting tumor progression and indicating a poor prognosis. These drugs can rebuild the body's anti-tumor immunity and effectively improve the survival outcomes of patients with advanced disease and platinum resistance. However, the efficacy of monotherapy is limited, with an effective rate of only 20% to 30%, accompanied by the risk of resistance and various adverse reactions. This study provides a theoretical reference for the clinical practice of immunotherapy for OSCC. Currently, the mechanisms of resistance and individualized treatment options remain unclear. In the future, it is necessary to precisely screen suitable candidates, continuously optimize combination treatment modes, and promote the standardized development of immunotherapy for OSCC.
References
[1] Loganathan S K, Schleicher K, Malik A, et al. Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signaling[J]. Science, 2020, 367(6483): 1264-1269.
[2] Wu X H. Study on the role and mechanism of STC1 in paclitaxel resistance of oral squamous cell carcinoma[D]. Beijing: Peking Union Medical College, 2025.
[3] Rahman R, Gopinath D, Buajeeb W, et al. Potential role of Epstein-Barr virus in oral potentially malignant disorders and oral squamous cell carcinoma: a scoping review[J]. Viruses, 2022, 14(4).
[4] Katirachi S K, Grønlund M P, Jakobsen K K, et al. The prevalence of HPV in oral cavity squamous cell carcinoma[J]. Viruses, 2023, 15(2).
[5] Glogauer J E, Sun C X, Bradley G, et al. Neutrophils increase oral squamous cell carcinoma invasion through an invadopodiadependent pathway[J]. Cancer Immunology Research, 2015, 3(11): 1218-1226.
[6] Wang Z Y. Study on the dynamic changes and targeting value of Treg cells in the occurrence and development of oral squamous cell carcinoma[D]. Beijing: Peking Union Medical College, 2025.
[7] Chen J, Jiang C C, Jin L, et al. Regulation of PD-L1: a novel emerging signalling in cancer[J]. Annals of Oncology, 2016, 27: 409-416.
[8] Burrack A L, Spartz E J, Raynor J F, et al. Combination PD-1 and PD-L1 blockade promotes durable neoantigen-specific T cell-mediated immunity in pancreatic ductal adenocarcinoma[J]. Cell Reports, 2019, 28(8): 2140-2155.e6.
[9] Boxberg M, Leising L, Steiger K, et al. Composition and clinical impact of the immunologic tumor microenvironment in oral squamous cell carcinoma[J]. Journal of Immunology, 2019, 202(1): 278-291.
[10] Tian G Y, Lu G Y, Lv Z J, et al. Expression significance of PD-1 and PD-L1 in oral squamous cell carcinoma and their prognostic value[J]. Journal of Practical Stomatology, 2021, 37(6): 841-844.
[11] Ma L J, Feng F L, Dong L Q, et al. Clinical significance of PD-1/PD-Ls gene amplification and overexpression in patients with hepatocellular carcinoma[J]. Theranostics, 2018, 8(20): 5690-5702.
[12] Jie W W, Qian L, Gen P A, et al. Neoadjuvant tislelizumab combined with chemotherapy in locally advanced oral or oropharyngeal squamous cell carcinoma: a real-world retrospective study[J]. Frontiers in Immunology, 2023, 14: 1282629.
Downloads
Published
Issue
Section
License
Copyright (c) 2026 by the authors.

This work is licensed under a Creative Commons Attribution 4.0 International License.
