Division of Medical Oncology, Department of Medicine, University of Washington, Seattle.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
JAMA. 2022 Feb 1;327(5):464-477. doi: 10.1001/jama.2022.0003.
Multiple myeloma is a hematologic malignancy characterized by presence of abnormal clonal plasma cells in the bone marrow, with potential for uncontrolled growth causing destructive bone lesions, kidney injury, anemia, and hypercalcemia. Multiple myeloma is diagnosed in an estimated 34 920 people in the US and in approximately 588 161 people worldwide each year.
Among patients with multiple myeloma, approximately 73% have anemia, 79% have osteolytic bone disease, and 19% have acute kidney injury at the time of presentation. Evaluation of patients with possible multiple myeloma includes measurement of hemoglobin, serum creatinine, serum calcium, and serum free light chain levels; serum protein electrophoresis with immunofixation; 24-hour urine protein electrophoresis; and full-body skeletal imaging with computed tomography, positron emission tomography, or magnetic resonance imaging. The Revised International Staging System combines data from the serum biomarkers β2 microglobulin, albumin, and lactate dehydrogenase in conjunction with malignant plasma cell genomic features found on fluorescence in situ hybridization-t(4;14), del(17p), and t(14;16)-to assess estimated progression-free survival and overall survival. At diagnosis, 28% of patients are classified as having Revised International Staging stage I multiple myeloma, and these patients have a median 5-year survival of 82%. Among all patients with multiple myeloma, standard first-line (induction) therapy consists of a combination of an injectable proteasome inhibitor (ie, bortezomib), an oral immunomodulatory agent (ie, lenalidomide), and dexamethasone and is associated with median progression-free survival of 41 months, compared with historical reports of 8.5 months without therapy. This induction therapy combined with autologous hematopoietic stem cell transplantation followed by maintenance lenalidomide is standard of care for eligible patients.
Approximately 34 920 people in the US and 155 688 people worldwide are diagnosed with multiple myeloma each year. Induction therapy with an injectable proteasome inhibitor, an oral immunomodulatory agent and dexamethasone followed by treatment with autologous hematopoietic stem cell transplantation, and maintenance therapy with lenalidomide are among the treatments considered standard care for eligible patients.
多发性骨髓瘤是一种血液恶性肿瘤,其特征是骨髓中存在异常克隆浆细胞,具有潜在的不受控制的生长能力,导致破坏性骨病变、肾损伤、贫血和高钙血症。在美国,每年约有 34920 人被诊断为多发性骨髓瘤,在全球约有 588161 人。
在多发性骨髓瘤患者中,约 73%有贫血,79%有溶骨性骨病,19%在就诊时患有急性肾损伤。对疑似多发性骨髓瘤患者的评估包括血红蛋白、血清肌酐、血清钙和血清游离轻链水平的测量;血清蛋白电泳加免疫固定;24 小时尿蛋白电泳;以及全身骨骼 CT、正电子发射断层扫描或磁共振成像。修订后的国际分期系统结合了血清生物标志物β2 微球蛋白、白蛋白和乳酸脱氢酶的数据,以及荧光原位杂交检测到的恶性浆细胞基因组特征 t(4;14)、del(17p)和 t(14;16),以评估估计的无进展生存期和总生存期。在诊断时,28%的患者被归类为修订后的国际分期系统 I 期多发性骨髓瘤,这些患者的中位 5 年生存率为 82%。在所有多发性骨髓瘤患者中,标准一线(诱导)治疗包括注射用蛋白酶体抑制剂(如硼替佐米)、口服免疫调节剂(如来那度胺)和地塞米松联合治疗,中位无进展生存期为 41 个月,而历史上无治疗的中位无进展生存期为 8.5 个月。这种诱导治疗联合自体造血干细胞移植,随后用来那度胺维持治疗是适合患者的标准治疗。
在美国,每年约有 34920 人,全球约有 155688 人被诊断为多发性骨髓瘤。注射用蛋白酶体抑制剂、口服免疫调节剂和地塞米松联合诱导治疗,随后自体造血干细胞移植治疗,以及来那度胺维持治疗是适合患者的标准治疗之一。