Predictive factors in the treatment of oral squamous cell carcinoma using PD-1/PD-L1 inhibitors
- PMID: 33594603
- DOI: 10.1007/s10637-021-01082-w
Predictive factors in the treatment of oral squamous cell carcinoma using PD-1/PD-L1 inhibitors
Abstract
Due to immune impairment and lymphocyte enrichment of oral squamous cell carcinoma (OSCC), anti-PD-1/PD-L1 therapy is regarded as a potential treatment option. However, tumor heterogeneity, differences in the immune conditions of patients, and the interrelation between tumor cells and stromal cells within the tumor microenvironment (TME) could affect the therapeutic efficacy of immune checkpoint blockades. Therefore, to maximize the benefit of blockade PD-1/PD-L1 axis, to find an efficient predictor (the possible clinical parameters or biological factors) before treatment are of great importance. In this review, we discuss the advantages of anti-PD-1/PD-L1 therapy for OSCC patients and find three respects that are currently available in predicting curative effect. Firstly, OSCC with high PD-L1 expression evaluating by immunohistochemistry (high tumor proportion score (TPS) and combined positive score (CPS)) are considered to be suitable for anti-PD-1/PD-L1 therapy. Secondly, gene-level predictive biomarkers including high metastatic mismatch repair deficiency (dMMR) signature or enrichment of interferon-γ and PD1 signaling pathway is expected to be favorable factors. Besides, PET/CT parameters (SUVmax, MTV, TLG) are proved to be correlated with PD-L1 expression, and some newly developed immunoPET probes are enlarging the application of PET/CT in predicting therapeutic efficacy of PD-1/PD-L1 inhibitors.
Keywords: Gene signature; Immunohistochemistry; Oral squamous cell carcinoma; PD-1/PD-L1 inhibitors; PET-CT.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.
Similar articles
-
Triptolide suppresses oral cancer cell PD-L1 expression in the interferon-γ-modulated microenvironment in vitro, in vivo, and in clinical patients.Biomed Pharmacother. 2021 Jan;133:111057. doi: 10.1016/j.biopha.2020.111057. Epub 2020 Dec 4. Biomed Pharmacother. 2021. PMID: 33378962
-
The Evolving Landscape of PD-1/PD-L1 Pathway in Head and Neck Cancer.Front Immunol. 2020 Sep 18;11:1721. doi: 10.3389/fimmu.2020.01721. eCollection 2020. Front Immunol. 2020. PMID: 33072064 Free PMC article. Review.
-
Clinical and Biological Significance of PD-L1 Expression Within the Tumor Microenvironment of Oral Squamous Cell Carcinoma.Anticancer Res. 2019 Jun;39(6):3039-3046. doi: 10.21873/anticanres.13437. Anticancer Res. 2019. PMID: 31177146
-
Cytotoxic T Lymphocyte Density and PD-L1 Expression Predict the Response to Anti-PD1 Therapy in Recurrent Oral Squamous Cell Carcinoma.Microbiol Immunol. 2025 Jun;69(6):350-358. doi: 10.1111/1348-0421.13220. Epub 2025 Apr 13. Microbiol Immunol. 2025. PMID: 40221937
-
PD-L1 expression in the microenvironment and the response to checkpoint inhibitors in head and neck squamous cell carcinoma.Oncoimmunology. 2020 Nov 19;9(1):1844403. doi: 10.1080/2162402X.2020.1844403. Oncoimmunology. 2020. PMID: 33299655 Free PMC article. Review.
Cited by
-
Inhibition of UFM1 expression suppresses cancer progression and is linked to the dismal prognosis and immune infiltration in oral squamous cell carcinoma.Aging (Albany NY). 2023 Nov 17;15(22):13059-13076. doi: 10.18632/aging.205219. Epub 2023 Nov 17. Aging (Albany NY). 2023. PMID: 37980168 Free PMC article.
-
Integrative analysis revealed a correlation of PIAS family genes expression with prognosis, immunomodulation and chemotherapy.Eur J Med Res. 2024 Mar 25;29(1):195. doi: 10.1186/s40001-024-01795-7. Eur J Med Res. 2024. PMID: 38528630 Free PMC article.
-
Expression of PD-L1 and p-RPS6 in epithelial dysplasia and squamous cell carcinoma of the oral cavity.Front Oral Health. 2024 Feb 2;5:1337582. doi: 10.3389/froh.2024.1337582. eCollection 2024. Front Oral Health. 2024. PMID: 38370876 Free PMC article.
-
Towards multiomic analysis of oral mucosal pathologies.Semin Immunopathol. 2023 Jan;45(1):111-123. doi: 10.1007/s00281-022-00982-0. Epub 2023 Feb 15. Semin Immunopathol. 2023. PMID: 36790488 Free PMC article. Review.
-
Nanosized Shikonin Disrupts Tumor-Cell Mismatch Repair and Synergizes with Manganese to Sensitize Squamous Carcinoma to Immunotherapy.ACS Nano. 2025 Apr 15;19(14):13889-13905. doi: 10.1021/acsnano.4c17090. Epub 2025 Apr 7. ACS Nano. 2025. PMID: 40190094 Free PMC article.
References
-
- de Vicente JC, Rodriguez-Santamarta T, Rodrigo JP, Blanco-Lorenzo V, Allonca E, Garcia-Pedrero JM (2019) PD-L1 expression in tumor cells is an independent unfavorable prognostic factor in oral squamous cell carcinoma. Cancer Epidemiol Biomark Prev 28(3):546–554. https://doi.org/10.1158/1055-9965.EPI-18-0779 - DOI
-
- Seiwert TY, Burtness B, Mehra R, Weiss J, Berger R, Eder JP, Heath K, McClanahan T, Lunceford J, Gause C, Cheng JD, Chow LQ (2016) Safety and clinical activity of pembrolizumab for treatment of recurrent or metastatic squamous cell carcinoma of the head and neck (KEYNOTE-012): an open-label, multicentre, phase 1b trial. Lancet Oncol 17(7):956–965. https://doi.org/10.1016/S1470-2045(16)30066-3 - DOI - PubMed
-
- Ferris RL, Blumenschein G Jr, Fayette J, Guigay J, Colevas AD, Licitra L, Harrington K, Kasper S, Vokes EE, Even C, Worden F, Saba NF, Iglesias Docampo LC, Haddad R, Rordorf T, Kiyota N, Tahara M, Monga M, Lynch M, Geese WJ, Kopit J, Shaw JW, Gillison ML (2016) Nivolumab for recurrent squamous-cell carcinoma of the head and neck. N Engl J Med 375(19):1856–1867. https://doi.org/10.1056/NEJMoa1602252 - DOI - PubMed - PMC
-
- Kaidar-Person O, Gil Z, Billan S (2018) Precision medicine in head and neck cancer. Drug Resist Updat 40:13–16. https://doi.org/10.1016/j.drup.2018.09.001 - DOI - PubMed
-
- Takahashi H, Sakakura K, Arisaka Y, Tokue A, Kaira K, Tada H, Higuchi T, Okamoto A, Tsushima Y, Chikamatsu K (2019) Clinical and Biological Significance of PD-L1 Expression Within the Tumor Microenvironment of Oral Squamous Cell Carcinoma. Anticancer Res 39(6):3039–3046. https://doi.org/10.21873/anticanres.13437 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials