Borumandi Farzad, Aghaloo Tara, Cascarini Luke, Gaggl Alexander, Fasanmade Kunmi
Oxford University Hospitals, Department of Oral, and Maxillofacial Surgery, Churchill Hospital and, John Radcliffe Hospital, Oxford, United Kingdom.
Anticancer Agents Med Chem. 2015;15(6):736-43. doi: 10.2174/1871520615666150325232857.
This article aims to give an overview on etiology, diagnosis and treatment options of osteonecrosis of the jaw bone among cancer patients receiving anti-resorptive drugs (ARDs). The physiologic bone function of continuous resorption and buildup is modified by the use of ARDs. Although ARDs proved to reduce pain and to improve the quality of life in patients with metastasizing bone disease, side effects such as medication related osteonecrosis of jaw bone (MRONJ) have been frequently reported since ARDs were firstly introduced. The new generation of ARDs such as Denosumab is associated with the same incidence of MRONJ among cancer patients. The etiology of MRONJ is not entirely understood and many hypotheses have been proposed. ARDs can modify the hard tissues directly by accumulation in the bone, or indirectly by suppression of the osteoclasts, inhibition of angiogenesis and vascularity. Some ARDs such as Bisphosphonates have reportedly the capacity to interfere directly and indirectly with the bone physiology. MRONJ can be a debilitating disease with non healing freely exposed bone in the oral cavity in patients, who already suffer from a primary cancerous disease. Knowledge of MRONJ as a potential side effect of ARDs is crucial for health professionals treating patients with bone modulating drugs.
本文旨在概述接受抗吸收药物(ARDs)的癌症患者颌骨坏死的病因、诊断和治疗选择。ARDs的使用改变了骨持续吸收和重塑的生理功能。尽管ARDs已被证明可减轻转移性骨病患者的疼痛并改善其生活质量,但自首次引入ARDs以来,诸如药物相关性颌骨坏死(MRONJ)等副作用屡有报道。新一代的ARDs,如地诺单抗,在癌症患者中与MRONJ的发生率相同。MRONJ的病因尚未完全明确,人们提出了许多假说。ARDs可通过在骨中蓄积直接改变硬组织,或通过抑制破骨细胞、抑制血管生成和血管形成间接改变硬组织。据报道,一些ARDs,如双膦酸盐,有直接和间接干扰骨生理的能力。MRONJ可能是一种使人衰弱的疾病,对于已经患有原发性癌症的患者,其口腔内的骨暴露无法自行愈合。了解MRONJ作为ARDs的潜在副作用,对于治疗使用骨调节药物患者的医疗专业人员至关重要。