Nanotechnology-based approaches for head and neck cancer treatment
Head and neck squamous cell carcinoma (HNSCC) continues to present with a poor prognosis and limited survival gains despite advances in multimodal management. In recent years, novel therapeutic approaches such as immunotherapy, proteolysis-targeting chimeras (PROTACs), and antibody-drug conjugates (ADCs) have expanded the treatment landscape. However, significant challenges remain regarding resistance, toxicity, and patient stratification. Nanotechnology-based drug delivery systems (DDS) represent a complementary strategy with the potential to enhance efficacy and minimize adverse effects by improving solubility, stability, biodistribution, and tumor-specific accumulation of anticancer agents. In this review, we summarize the development of different DDS platforms encapsulating either cisplatin or small-molecule inhibitors, highlighting preclinical studies and clinical trials in HNSCC. A particular emphasis is placed on the distinction between passive and active targeting strategies, offering a comprehensive overview of how nanoparticle functionalization and tumor-selective delivery can further enhance therapeutic outcomes. This dual perspective underscores the translational opportunities of nanomedicine within the evolving landscape of HNSCC treatment.
Authors
- Corina Lorz (ORCID: https://orcid.org/0000-0001-8214-9076)
- Carlos Alonso‐Moreno (ORCID: https://orcid.org/0000-0002-7588-0781)
- Iván Bravo (ORCID: https://orcid.org/0000-0003-1589-5399)
- Almudena del Campo-Balguerías (ORCID: https://orcid.org/0000-0002-0119-6733)
- Alberto Ocaña (ORCID: https://orcid.org/0000-0002-1067-9630)
Institutions
- Research Institute Hospital 12 de Octubre (ES)
- Hospital Universitario Fundación Jiménez Díaz (ES)
- Centro de Investigación Biomédica en Red de Cáncer (ES)
- University of Castilla-La Mancha (ES)
Publication Details
- Journal
- Biomedicine & Pharmacotherapy
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1016/j.biopha.2025.118871
- Primary Topic
- Protein Degradation and Inhibitors
- Type
- article
- Field-Weighted Citation Impact
- 0.00