Abstract

Head and neck cancer (HNC) is a heterogeneous disease that includes a variety of tumors originating in the hypopharynx, oropharynx, lip, oral cavity, nasopharynx, or larynx. HNC is the sixth most common malignancy worldwide and affects thousands of people in terms of incidence and mortality. Various factors can trigger the development of the disease such as smoking, alcohol consumption, and repetitive viral infections. HNC is currently treated by single or multimodality approaches, which are based on surgery, radiotherapy, chemotherapy, and biotherapeutic antibodies. The latter approach will be the focus of this article. There are currently three approved antibodies against HNCs (cetuximab, nivolumab, and pembrolizumab), and 48 antibodies under development. The majority of these antibodies are of humanized (23 antibodies) or human (19 antibodies) origins, and subclass IgG1 represents a total of 32 antibodies. In addition, three antibody drug conjugates (ADCs: telisotuzumab-vedotin, indatuximab-ravtansine, and W0101) and two bispecific antibodies (GBR 1372 and ABL001) have been under development. Despite the remarkable success of antibodies in treating different tumors, success was limited in HNCs. This limitation is attributed to efficacy, resistance, and the appearance of various side effects. However, the efficacy of these antibodies could be enhanced through conjugation to gold nanoparticles (GNPs). These conjugates combine the high specificity of antibodies with unique spectral properties of GNPs to generate a treatment approach known as photothermal therapy. This approach can provide promising outcomes due to the ability of GNPs to convert light into heat, which can specifically destroy cancer cells and treat HNC in an effective manner.

Highlights

  • Antibodies for the Treatment of Head and Neck Cancer: Current Approaches and Future Considerations of Photothermal Therapies

  • The current treatment standard for recurring or metastatic Head and neck cancer (HNC) is based on cetuximab and platinum based cisplatin or carboplatin CT plus methotrexate and 5-flurouracil; which is further strengthened by surgery and RT, and occasionally augmented by paclitaxel and docetaxel [11]

  • The HNC treatment approaches are based on surgery, RT, CT, and biotherapeutic antibodies

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Summary

13 Monalizumab Innate Pharma SA and AstraZeneca

Utomilumab MorphoSys AG, Pfizer Inc IgG2 Cixutumumab ImClone Systems (Eli Lilly) IgG1. CD94/NK group 2 member A (NKG2A) CD137 (4-1BB) Insulin-like growth factor 1 (IGF-1) receptor HER3. NCT03019003 (phase I/II) NCT03162224 (phase I/II) NCT02291055 (phase I/II) NCT02997332 (phase I) NCT02551159 (phase III) NCT03829007 (phase I/II) NCT02369874 (phase III) NCT03737968 (phase II) NCT03051906 (phase I/II) NCT03258554 (phase II/III) NCT03691714 (phase II) NCT02207530 (phase II) NCT02319044 (phase II) NCT03292250 (phase II) NCT02318277 (phase I/II) NCT02423863 (phase II) NCT03518606 (phase I/II) NCT02499328 (phase I/II) NCT04262388 (phase II) NCT03983954 (phase I) NCT03212469 (phase I/II) NCT03739931 (phase I) NCT02052960 (phase II)

38 Hu5F9-G4 39 W0101
48 Ipilimumab
Albumin stabilized NP and paclitaxel
Findings
CONCLUSIONS
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