Dao Aiken, McDonald Michelle M, Savage Paul B, Little David G, Schindeler Aaron
Bioengineering & Molecular Medicine Laboratory, The Children's Hospital at Westmead and the Westmead Institute for Medical Research, Sydney, New South Wales, Australia.
Children's Hospital Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
J Bone Oncol. 2022 Oct 28;37:100460. doi: 10.1016/j.jbo.2022.100460. eCollection 2022 Dec.
Multiple myeloma is a hematological malignancy affecting the plasma cells. It is the second most common hematologic cancer in adults. Over 90% of patients develop local osteolytic lesions and skeletal-related events at some point during the progression of the disease. Bone lesions can induce severe pain and immobility and can also increase the risk of fractures and osteomyelitis. Skeletal complications are associated with poor clinical outcomes, affecting quality of life and mortality. Current standards of care for myeloma, e.g., autologous stem-cell transplantation (ASCT) and chemotherapy, do not lessen the risk of adverse events in bone. Once bone lesions are present, bone-targeted interventions are limited, with bone antiresorptive drugs being a mainstay of treatment. This review highlights the growing literature surrounding osteolytic lesions and bone infections associated with multiple myeloma and assesses current and emerging treatments. Emerging evidence from clinical trials suggests that denosumab can reduce skeletal-related events, and the potential application of bortezomib/1D11 can reduce bone destruction and pathological fractures in MM patients. Once established, bone lesions are prone to develop osteomyelitis - especially in immunocompromised individuals. Antibiotics and surgical interventions have been used to manage bone infections in most reported cases. As the bone infection risk associated with MM bone lesions become more evident, there is scope to improve patient management by mitigating this risk with prophylactic antimicrobial therapy.
多发性骨髓瘤是一种影响浆细胞的血液系统恶性肿瘤。它是成人中第二常见的血液系统癌症。超过90%的患者在疾病进展的某个阶段会出现局部溶骨性病变和骨相关事件。骨病变可引发严重疼痛和活动障碍,还会增加骨折和骨髓炎的风险。骨骼并发症与不良临床结局相关,影响生活质量和死亡率。目前骨髓瘤的治疗标准,如自体干细胞移植(ASCT)和化疗,并未降低骨骼不良事件的风险。一旦出现骨病变,针对骨骼的干预措施有限,骨吸收抑制剂是主要的治疗手段。本综述重点介绍了围绕多发性骨髓瘤相关溶骨性病变和骨感染的不断增多的文献,并评估了当前及新兴的治疗方法。临床试验的新证据表明,地诺单抗可减少骨相关事件,硼替佐米/1D11的潜在应用可减少MM患者的骨质破坏和病理性骨折。一旦形成,骨病变容易发展为骨髓炎——尤其是在免疫功能低下的个体中。在大多数报告的病例中,抗生素和手术干预已被用于治疗骨感染。随着与MM骨病变相关的骨感染风险变得更加明显,通过预防性抗菌治疗降低这种风险,有改善患者管理的空间。