Advances in Nanoplatform Design and Theranostics for HNC via the Tumor Microenvironment

Ngwu Chukwuebuka Vitalis, Ying Wang, Afreh Paul, Anidobu Chinaecherem Grace

Head and neck cancer; Tumor microenvironment; Nanoplatform; Nanotheranostics; Imaging; Targeted therapy.

Head and neck cancer (HNC) accounts for approximately 930,000 new cases and 470,000 deaths annually, with squamous cell carcinoma (HNSCC) of the upper aerodigestive tract representing the dominant histology. Tobacco use, alcohol consumption and high-risk human papillomavirus infection are the principal risk factors. Standard-of-care modalities such as surgery, radiotherapy, chemotherapy and photodynamic therapy frequently fail in advanced disease because of off-target toxicity and inherent or acquired resistance. Recent insights into the tumor microenvironment (TME) characterized by hypoxia, acidic pH, extracellular-matrix remodeling and immunosuppression have revealed actionable therapeutic targets. This review synthesizes how nanotechnology exploits these TME features to enhance HNC diagnosis and treatment. We first delineate the unique TME landscape of HNSCC and then classify TME-responsive nanoplatforms according to their design principles: pH, redox, enzyme or hypoxia-triggered release; active targeting of overexpressed receptors; and multimodal theranostics. Subsequent sections evaluate diagnostic applications (MRI, CT, PET, optical and molecular imaging) and therapeutic strategies, including chemotherapy delivery, immunomodulation and combination regimens. Finally, we address translational bottlenecks biocompatibility, manufacturing scalability, tumor heterogeneity, regulatory complexity and propose precision-nanomedicine solutions. Pre-clinical studies demonstrate that TME-activated nanoplatforms achieve superior tumor accumulation, reduced systemic toxicity and integrated imaging-therapy functions. Multifunctional nanocarriers that co-load chemotherapeutics, photosensitizers and immune checkpoint inhibitors further exhibit synergistic anti-tumor activity. Although challenges related to biodistribution, batch-to-batch reproducibility and patient stratification persist. Interdisciplinary efforts spanning materials science, oncology and regulatory science are poised to accelerate the clinical translation of TME-focused nanotheranostics toward individualized HNC management.

Received: 25 Aug 2025, Received in revised form: 23 Sep 2025, Accepted: 27 Sep 2025, Available online: 30 Sep 2025

10.22161/ijaers.1210.1