Evidence map›Paper›PMID 42317269›Full record

ReviewFrontiers in cell and developmental biology2026

Precision immuno-oncology in oral cancer: latest trends in biomarkers, novel drug development and nanoparticle-based therapeutic platforms.

Dominic Augustine, Samudrala Venkatesiah Sowmya, C Pushpalatha, Kavitha Prasad, Hajira Khatoon

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Dominic AugustineDepartment of Oral and Maxillofacial Pathology and Oral Microbiology, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
Samudrala Venkatesiah SowmyaDepartment of Oral and Maxillofacial Pathology and Oral Microbiology, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
C PushpalathaDepartment of Pediatric and Preventive Dentistry, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
Kavitha PrasadDepartment of Oral and Maxillofacial Surgery, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
Hajira KhatoonDepartment of Oral and Maxillofacial Surgery, Faculty of Dental Sciences, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma poses a significant global health burden, with over 370,000 annual cases and poor 5-year survival rates of 50%-60%, driven by risk factors like tobacco and alcohol. Despite advances in surgery, radiotherapy, and chemotherapy, functional morbidity and resistance necessitate precision immuno-oncology approaches. This review explores the tumour immune microenvironment in oral squamous cell carcinoma, characterized by immunosuppressive elements like M2 macrophages, myeloid-derived suppressor cells, and regulatory T cells, alongside spatial heterogeneity that complicates therapy. Biomarkers for patient selection include programmed death-ligand1 expression (via combined positive scoring), tumour mutational burden, neoantigen load, interferon-gamma-γ signatures, cytolytic scores, peripheral circulating tumour DNA, and single-cell/spatial profiling, though standardization remains critical. Immunotherapy has transformed oral squamous cell carcinoma management, with programmed cell death protein-1 inhibitors like nivolumab and pembrolizumab showing survival benefits in trials, particularly in programmed cell death protein-L1-positive cases. Emerging strategies encompass next-generation checkpoints (Lymphocyte activation gene-3, T-cell immunoreceptor with Ig and ITIM domains, OX40), personalized neoantigen vaccines, adoptive cell therapies (Tumour-Infiltrating Lymphocytes, Chimeric Antigen Receptor T-cell therapy), and rational combinations to counter resistance. Nanomedicine platforms-liposomes, polymeric nanoparticles, gold-based systems-enhance drug delivery, reprogram the Tumour and immune microenvironment, and enable chemo-immuno-photothermal synergies, addressing mucosal barriers and toxicity. Future priorities include biomarker validation via prospective registries, scalable Good Manufacturing Practice nanoplatforms, AI-driven multi-omic modeling, and federated learning for predictive analytics. By integrating tumour genomics, immune profiling, and advanced delivery, precision immuno-oncology holds promise to improve response rates, durability, and quality of life in oral squamous cell carcinoma.

Indexed as

biomarkersimmunotherapynanomedicineoral squamous cell carcinomaprecision immuno-oncologyprogrammed death-ligand 1tumor immune microenvironment

Identifiers

PMID42317269
PMCPMC13271877

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.