• Review of 37 RCTs on chemopreventive agents for OSCC and OPMDs. • Retinoids show efficacy but limited by toxicity and recurrence. • Antioxidants inconsistent, some with harmful effects. • Herbal and natural agents show promising lesion regression. • Combination and targeted therapies offer future potential. Oral squamous cell carcinoma (OSCC) is a significant global health concern, often developing from oral potentially malignant disorders (OPMDs). Given the poor prognosis associated with late-stage OSCC, there is growing interest in chemoprevention as a strategy to halt or reverse malignant transformation. This systematic review evaluated 37 randomised controlled trials examining the effectiveness of various chemopreventive agents, including retinoids, antioxidants, herbal compounds, immune checkpoint inhibitors, and anti-inflammatory drugs. Retinoids demonstrated potential in reducing second primary tumors and malignant progression but were hindered by toxicity and high recurrence rates. Antioxidants showed limited preventive benefit, though they may alleviate treatment-related side effects. Herbal agents and combination therapies, such as those containing β-carotene, isotretinoin, IFN-α 2a, and vitamin E, have shown encouraging results, although the long-term benefits remain uncertain. Novel approaches, including COX-2 inhibitors and immunotherapies, appear promising but need further validation. While chemopreventive strategies offer potential, their clinical application remains limited by inconsistent outcomes and adverse effects. Advancing this field requires the development of targeted therapies, personalised approaches based on molecular profiling, and innovative delivery systems like nanocarriers to improve therapeutic efficacy and safety.
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Faris M Alabeedi
The University of Western Australia
Mengwen Zheng
The University of Western Australia
Anchal Kataria
Oral Oncology
The University of Western Australia
Qatar University
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Alabeedi et al. (Sat,) studied this question.
synapsesocial.com/papers/69d49ecbb33cc4c35a2277ed — DOI: https://doi.org/10.1016/j.oraloncology.2026.107961
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