Sanwick Alexis M, Chaple Ivis F
Department of Nuclear Engineering, University of Tennessee, Knoxville, TN, United States.
Front Oncol. 2024 Aug 22;14:1445191. doi: 10.3389/fonc.2024.1445191. eCollection 2024.
Head and neck squamous cell carcinoma (HNSCC) is a type of head and neck cancer that is aggressive, difficult to treat, and often associated with poor prognosis. HNSCC is the sixth most common cancer worldwide, highlighting the need to develop novel treatments for this disease. The current standard of care for HNSCC usually involves a combination of surgical resection, radiation therapy, and chemotherapy. Chemotherapy is notorious for its detrimental side effects including nausea, fatigue, hair loss, and more. Radiation therapy can be a challenge due to the anatomy of the head and neck area and presence of normal tissues. In addition to the drawbacks of chemotherapy and radiation therapy, high morbidity and mortality rates for HNSCC highlight the urgent need for alternative treatment options. Immunotherapy has recently emerged as a possible treatment option for cancers including HNSCC, in which monoclonal antibodies are used to help the immune system fight disease. Combining monoclonal antibodies approved by the US Food and Drug Administration, such as cetuximab and pembrolizumab, with radiotherapy or platinum-based chemotherapy for patients with locally advanced, recurrent, or metastatic HNSCC is an accepted first-line therapy. Targeted radionuclide therapy can potentially be used in conjunction with the first-line therapy, or as an additional treatment option, to improve patient outcomes and quality of life. Epidermal growth factor receptor is a known molecular target for HNSCC; however, other targets such as human epidermal growth factor receptor 2, human epidermal growth factor receptor 3, programmed cell death protein 1, and programmed death-ligand 1 are emerging molecular targets for the diagnosis and treatment of HNSCC. To develop successful radiopharmaceuticals, it is imperative to first understand the molecular biology of the disease of interest. For cancer, this understanding often means detection and characterization of molecular targets, such as cell surface receptors, that can be used as sensitive targeting agents. The goal of this review article is to explore molecular targets for HNSCC and dissect previously conducted research in nuclear medicine and provide a possible path forward for the development of novel radiopharmaceuticals used in targeted radionuclide therapy for HNSCC, which has been underexplored to date.
头颈部鳞状细胞癌(HNSCC)是一种侵袭性强、难以治疗且预后通常较差的头颈部癌症。HNSCC是全球第六大常见癌症,这凸显了开发针对该疾病新疗法的必要性。HNSCC目前的标准治疗通常包括手术切除、放射治疗和化疗。化疗因其有害的副作用而声名狼藉,这些副作用包括恶心、疲劳、脱发等等。由于头颈部区域的解剖结构以及正常组织的存在,放射治疗可能具有挑战性。除了化疗和放射治疗的缺点外,HNSCC的高发病率和死亡率凸显了对替代治疗方案的迫切需求。免疫疗法最近已成为包括HNSCC在内的癌症的一种可能治疗选择,其中单克隆抗体用于帮助免疫系统对抗疾病。将美国食品药品监督管理局批准的单克隆抗体,如西妥昔单抗和帕博利珠单抗,与放疗或铂类化疗联合用于局部晚期、复发或转移性HNSCC患者是一种公认的一线治疗方法。靶向放射性核素治疗有可能与一线治疗联合使用,或作为一种额外的治疗选择,以改善患者的治疗效果和生活质量。表皮生长因子受体是HNSCC已知的分子靶点;然而,其他靶点,如人表皮生长因子受体2、人表皮生长因子受体3、程序性细胞死亡蛋白1和程序性死亡配体1,正成为HNSCC诊断和治疗的新兴分子靶点。为了开发成功的放射性药物,首先必须了解相关疾病的分子生物学。对于癌症来说,这种了解通常意味着检测和表征分子靶点,如细胞表面受体,这些靶点可用作敏感的靶向剂。这篇综述文章的目的是探索HNSCC的分子靶点,剖析先前在核医学方面进行的研究,并为开发用于HNSCC靶向放射性核素治疗的新型放射性药物提供一条可能的前进道路,而这一领域迄今为止尚未得到充分探索。