Popovici Ion Alexandru, Kajanto Lidia Anca, Popovici Laura Roxana, Augustin Iolanda Georgiana, Gales Laurentia Nicoleta
Department of Implant Prosthetic Therapy, Faculty of Dentistry, University of Medicine and Pharmacy "Carol Davila" Bucharest, 010221 Bucharest, Romania.
Institute of Oncology "Alexandru Trestioreanu", 022328 Bucharest, Romania.
Cancers (Basel). 2025 Mar 21;17(7):1061. doi: 10.3390/cancers17071061.
This review systematically examines the oral complications associated with conventional and novel anti-cancer therapies. It highlights that while molecularly targeted agents including monoclonal antibodies targeting the vascular endothelial growth factor and its receptor, the epidermal growth factor receptor, tyrosine kinase inhibitors, and immune checkpoint inhibitors tend to exhibit a lower overall toxicity profile compared to traditional cytotoxic chemotherapeutics, they are nonetheless linked to significant oral adverse events. These complications encompass inflammatory mucosal reactions known as mucositis, salivary gland dysfunction leading to a sensation of dryness in the mouth, taste alterations referred to as dysgeusia, and, critically, medication-related osteonecrosis of the jaw. In particular, bone-modifying agents such as bisphosphonates and denosumab disrupt bone remodeling and the formation of new blood vessels, thereby increasing the susceptibility to osteonecrosis of the jaw, especially following invasive dental procedures. The review delineates the multifactorial pathogenesis underlying these toxicities, which involves direct cell toxicity, impaired wound healing, and secondary infections. Furthermore, it emphasizes the importance of pre-treatment dental evaluation and preventive strategies including patient education, prophylactic dental care, and the integration of adjunctive therapies such as laser therapy and autologous platelet concentrates to mitigate these adverse effects. The analysis advocates for interdisciplinary collaboration between oncologists and dental professionals to optimize management protocols, enhance treatment adherence, and ultimately improve the quality of life for oncology patients undergoing anti-cancer therapy.
本综述系统地研究了与传统和新型抗癌疗法相关的口腔并发症。研究强调,虽然包括靶向血管内皮生长因子及其受体的单克隆抗体、表皮生长因子受体、酪氨酸激酶抑制剂和免疫检查点抑制剂在内的分子靶向药物与传统细胞毒性化疗药物相比,总体毒性较低,但它们仍与严重的口腔不良事件有关。这些并发症包括称为黏膜炎的炎症性黏膜反应、导致口腔干燥感的唾液腺功能障碍、称为味觉障碍的味觉改变,以及至关重要的与药物相关的颌骨坏死。特别是,双膦酸盐和地诺单抗等骨改性剂会破坏骨重塑和新血管的形成,从而增加颌骨坏死的易感性,尤其是在进行侵入性牙科手术后。该综述阐述了这些毒性的多因素发病机制,包括直接细胞毒性、伤口愈合受损和继发性感染。此外,它强调了治疗前牙科评估和预防策略的重要性,包括患者教育、预防性牙科护理,以及整合激光治疗和自体血小板浓缩物等辅助疗法以减轻这些不良反应。该分析提倡肿瘤学家和牙科专业人员之间进行跨学科合作,以优化管理方案、提高治疗依从性,并最终改善接受抗癌治疗的肿瘤患者的生活质量。