de Daniel Anna, Rodríguez-Lobato Luis Gerardo, Tovar Natalia, Cibeira M Teresa, Moreno David F, Oliver-Caldés Aina, Isola Ignacio, Lozano Ester, Bladé Joan, Rosiñol Laura, Fernández de Larrea Carlos
Amyloidosis and Multiple Myeloma Unit, Department of Hematology, Hospital Clínic of Barcelona Universitat de Barcelona Barcelona Spain.
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Barcelona Spain.
Hemasphere. 2024 May 6;8(5):e76. doi: 10.1002/hem3.76. eCollection 2024 May.
The 2/20/20 International Myeloma Working Group (IMWG) score is the most employed risk score in clinical practice to evaluate the risk of progression from smoldering multiple myeloma (SMM) to symptomatic multiple myeloma. However, it faces a serious limitation: The risk score is applied at diagnosis and cannot be reapplied. Since a dynamic accurate patient risk assessment for progression is necessary, we aimed to investigate whether the detection of an evolving pattern in serum M-protein (SMP) improves the identification of high-risk patients. Eighty-three patients diagnosed with SMM between 2011 and 2020 were included. Patients were initially classified applying the 2/20/20 IMWG score at baseline and later reclassified depending on the presence of an SMP evolving pattern into six groups. We regrouped the patients into three final risk groups: low-risk, intermediate-risk, and high-risk. The risk of progression at two years for the high-risk group was 88% and all patients had progressed at 4 years. The performance measurements were superior for the new 2/20/20-Evolving score independently for the detection of high-risk patients. We show that the sequential measurement of the SMP is a noninvasive and widely available test that improves the 2/20/20 IMWG risk score.
2020年2月20日国际骨髓瘤工作组(IMWG)评分是临床实践中用于评估冒烟型多发性骨髓瘤(SMM)进展为症状性多发性骨髓瘤风险时最常用的风险评分。然而,它面临一个严重的局限性:该风险评分在诊断时应用,不能再次应用。由于对疾病进展进行动态准确的患者风险评估是必要的,我们旨在研究血清M蛋白(SMP)演变模式的检测是否能改善高危患者的识别。纳入了2011年至2020年间诊断为SMM的83例患者。患者最初在基线时应用2020年2月20日IMWG评分进行分类,随后根据SMP演变模式的存在情况重新分类为六组。我们将患者重新分组为三个最终风险组:低风险、中风险和高风险。高危组两年时的进展风险为88%,所有患者在4年时均已进展。新的2020年2月20日-演变评分在检测高危患者方面的性能指标独立更优。我们表明,SMP的序贯测量是一种非侵入性且广泛可用的检测方法,可改善2020年2月20日IMWG风险评分。