21世纪多发性骨髓瘤的单中心真实世界经验

Hyungwoo Cho, S. Kim, Kyoungmin Lee, E. Kang, J. Park, C. Suh
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摘要

背景/目的:韩国多发性骨髓瘤(MM)的发病率正在迅速上升。MM的诊断标准已经更新,新的治疗药物可用。本研究探讨在峨山医疗中心(AMC)登记的MM患者的特点和过去15年的预后。方法:数据来自AMC MM登记处,该登记处一直在前瞻性地收集MM患者的数据。我们分析中包括的774名MM患者是在2003年沙利度胺作为一种新型治疗剂可用时被诊断出来的,直到2019年4月。评估这些患者的2年生存率。患者根据年龄是否大于或小于65岁(65岁是自体干细胞移植适应症的截止年龄)分为两组。患者也根据诊断年份进行分组:到2006年,当硼替佐米可用,到2010年,当来那度胺的费用得到报销。结果:< 65岁的患者预后较好,表现为表现较好,病程较晚,FISH分析结果异常较少。将我们的韩国患者与澳大利亚和新西兰骨髓瘤相关疾病登记处登记的患者进行比较,发现了种族差异。所有患者的中位总生存期为3.7年,5年生存率为41.8%,10年生存率为23.4%。晚期确诊患者的生存率逐渐提高。年龄、运动状态、肾功能、c反应蛋白水平、乳酸脱氢酶水平和细胞遗传学结果被认为是重要的预后因素。结论:这项真实世界的调查揭示了21世纪初在韩国一家三级医院被诊断为MM的患者的临床特征和生存率。
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Single-Center Real-World Experience of Multiple Myeloma in the 21st Century
Background/Aims: The incidence of multiple myeloma (MM) in Korea is rapidly increasing. The diagnostic criteria of MM have been updated and novel therapeutic agents are available. This study explored the features of MM patients registered at Asan Medical Center (AMC) and the outcomes over the past 15 years.Methods: Data were obtained from the AMC MM registry, which has been collecting the data of MM patients prospectively. The 774 MM patients included in our analysis were diagnosed from 2003, when thalidomide became available as a novel therapeutic agent, until April 2019. The 2-year survival rate of these patients was assessed. Patients were divided into two groups based on whether they were older or younger than 65 years, which is the cutoff age for the indication of autologous stem cell transplantation. Patients were also grouped according to the year of diagnosis: up to 2006, when bortezomib became available, and up to 2010, when the cost of lenalidomide was reimbursed.Results: Patients < 65 years of age had better prognostic features, including a better performance, less advanced disease stage, and fewer abnormalities in their fluorescent in-situ hybridization (FISH) analysis results. A comparison of our Korean patients with patients registered in the Myeloma Related Disorder Registry data of Australia and New Zealand, showed ethnic discrepancies. The median overall survival of all patients was 3.7 years, with a 5-year survival rate of 41.8% and a 10-year survival rate of 23.4%. Survival progressively improved in patients diagnosed later. Age, performance status, renal function, C-reactive protein level, lactate dehydrogenase level, and cytogenetic findings were identified as significant prognostic factors.Conclusions: This real-world survey revealed the clinical features and survival rates of patients at a tertiary Korean Hospital who were diagnosed with MM at the beginning of 21st century.
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