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Denosumab-associated Osteonecrosis of the Jaw; A Case Series and Literature Review

机译:Denosumab相关的下颌骨坏死;案例系列与文献综述

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Introduction: Medication-related osteonecrosis of the jaw (MRONJ) is a severely debilitating condition of multifactorial pathogenesis. It primarily involves patients receiving intravenous bisphosphonates (BPs) and most recently the new antiresorptive drug, denosumab, for the treatment of skeletal-related malignancies. There is no curative treatment and no consensus exists regarding the clinical management of such patients. This review aims to share our current clinical experience at Sheffield Teaching Hospitals’ Trust and raise awareness of the increase in severity of ONJ in patients receiving denosumab. Patients and Methods: Four new cases with clinical diagnosis of MRONJ were presented to Sheffield Teaching Hospitals' Trust. MRONJ was attributed to denosumab therapy, as all patients were treated solely with denosumab for skeletal-related malignancies. Results: All cases appear to have a more aggressive mode of ONJ compared to that seen with IV and/or oral BPs so far. The cause of MRONJ was observed in the presence of periodontal disease alone and following dental extractions. Progression of the disease occurred considerably faster with the development of widespread suppuration and tooth mobility within weeks. Imaging revealed rather extensive areas of bony destruction, sometimes with associated periosteal reaction in keeping with a chronic bony infection. Conclusion: It is imperative for all dental and medical teams involved in treating these patients to understand the side effects of RANKL inhibitors on bone metabolism and how it affects treatment. Helping patients to understand the chronicity and potential progression of the disease is essential to a satisfactory outcome.
机译:简介:与药物有关的颌骨坏死(MRONJ)是多因素发病机制中的一种严重使人衰弱的疾病。它主要涉及接受静脉内双膦酸盐(BPs)治疗的患者,最近涉及接受新的抗吸收药物denosumab来治疗与骨骼相关的恶性肿瘤。对于此类患者的临床治疗尚无治疗方法,也未达成共识。这篇综述旨在分享我们在谢菲尔德教学医院信托基金会的当前临床经验,并提高人们对接受地诺单抗的ONJ严重程度增加的认识。患者与方法:向谢菲尔德教学医院信托基金呈交了4例新的MRONJ临床诊断病例。 MRONJ归因于denosumab治疗,因为所有患者均仅接受denosumab治疗与骨骼相关的恶性肿瘤。结果:到目前为止,与静脉和/或口服BP相比,所有病例似乎都具有更强的ONJ模式。仅在牙周疾病的存在下和拔牙后观察到MRONJ的原因。随着数周内化脓和牙齿活动性的发展,疾病的进展速度明显加快。影像学检查显示相当广泛的骨破坏区域,有时伴有骨膜反应,与慢性骨感染保持一致。结论:所有参与治疗这些患者的牙科和医疗团队都必须了解RANKL抑制剂对骨代谢的副作用及其对治疗的影响。帮助患者了解疾病的慢性和潜在进展对于取得令人满意的结果至关重要。

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