Katzel Jed A, Hari Parameswaran, Vesole David H
St. Vincent's Comprehensive Cancer Center, New York, NY, USA.
CA Cancer J Clin. 2007 Sep-Oct;57(5):301-18. doi: 10.3322/CA.57.5.301.
Multiple myeloma (MM) is an incurable clonal B-cell malignancy with terminally differentiated plasma cells. It afflicts approximately 55,000 people in the United States. Over the past 5 years, significant progress has been made in the diagnosis and assessment of patients with MM. Significant advances include a simplified staging system, which has replaced the more cumbersome Durie-Salmon staging system; an updated uniform international response criteria; the development of a sensitive new serum test to detect free light chain production (free light chain assay); the recognition of specific adverse cytogenetic abnormalities; and the evolution of genomics, which will identify specific and targeted therapies for individual MM patients. For the first time in decades, major therapeutic advances have been implemented in the treatment of MM patients. These include 2 new classes of agent: immunomodulatory drugs and proteosome inhibitors. In addition, clinical trials have solidified the role of hematopoietic stem cell transplant and established the benefits of post-transplant maintenance therapy. Finally, a number of new agents are in development that specifically target the myeloma cells and/or the bone marrow microenvironment. These advances have resulted in expanded treatment options, prolonged disease control and survival, and improved quality of life for patients with MM.
多发性骨髓瘤(MM)是一种无法治愈的克隆性B细胞恶性肿瘤,由终末分化的浆细胞构成。在美国,约有55000人罹患此病。在过去5年里,MM患者的诊断和评估取得了显著进展。重大进展包括:一个简化的分期系统取代了更为繁琐的Durie-Salmon分期系统;更新的统一国际缓解标准;一种用于检测游离轻链产生的新型敏感血清检测方法(游离轻链分析)的开发;特定不良细胞遗传学异常的识别;以及基因组学的发展,这将为个体MM患者确定特定的靶向治疗方法。几十年来,MM患者的治疗首次取得了重大进展。这些进展包括两类新型药物:免疫调节药物和蛋白酶体抑制剂。此外,临床试验巩固了造血干细胞移植的作用,并确立了移植后维持治疗的益处。最后,一些专门针对骨髓瘤细胞和/或骨髓微环境的新型药物正在研发中。这些进展为MM患者带来了更多的治疗选择、延长了疾病控制时间和生存期,并改善了生活质量。