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不明意义单克隆丙种球蛋白血症患者中既定风险分层模型的纵向评估。

Longitudinal assessment of established risk stratification models in patients with monoclonal gammopathy of undetermined significance.

机构信息

Heidelberg Myeloma Center, Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.

Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Blood Cancer J. 2024 Aug 27;14(1):148. doi: 10.1038/s41408-024-01126-3.

Abstract

Risk of progression of monoclonal gammopathy of undetermined significance (MGUS) into multiple myeloma and related plasma cell disorders can be determined by three major risk stratification models, namely Mayo2005, Sweden2014, and NCI2019. This retrospective study of 427 patients with MGUS diagnosed according to the 2014 International Myeloma Working Group criteria aimed to describe and analyze the longitudinal applicability of these risk models. In all three models, the majority of patients remained at their baseline risk group, whereas small numbers of patients migrated to a different risk group. Proportions of patients among risk groups remained stable over time (e.g. Mayo2005 model, low-risk group, at baseline: 43%, after 1, 2, 3, 4, 5, and 8 years: 40%, 37%, 37%, 43%, 44%, and 43%). All three risk models reliably distinguished risk of progression at baseline, upon yearly reassessment (e.g. 1 year from diagnosis) and in time-dependent analyses. Upstaging to a high-risk category was associated with an increased risk of progression in all three models (Mayo2005: hazard ratio [HR] = 5.43, 95% confidence interval [95% CI] 1.21-24.39, p = 0.027; Sweden2014: HR = 13.02, 95% CI 5.25-32.28, p < 0.001; NCI2019: HR = 5.85, 95% CI 2.49-13.74, p < 0.001). Our study shows that MGUS risk stratification models can be applied longitudinally to repeatedly determine and improve individual risk of progression. Patient migration to higher risk categories during follow up should prompt more frequent monitoring in clinical routine.

摘要

风险进展多发性骨髓瘤和相关浆细胞疾病的单克隆丙种球蛋白血症的不确定意义(MGUS)可以通过三个主要的风险分层模型来确定,即 Mayo2005、瑞典 2014 年和 NCI2019。本研究回顾性分析了 427 例按照 2014 年国际骨髓瘤工作组标准诊断为 MGUS 的患者,旨在描述和分析这些风险模型的纵向适用性。在所有三种模型中,大多数患者仍处于基线风险组,而少数患者转移到不同的风险组。随着时间的推移,风险组中的患者比例保持稳定(例如 Mayo2005 模型,低风险组,基线:43%,1、2、3、4、5 和 8 年后:40%、37%、37%、43%、44%和 43%)。所有三种风险模型都能可靠地区分基线时的进展风险,每年重新评估(例如诊断后 1 年)和时间依赖性分析。在所有三种模型中,向高危类别升级与进展风险增加相关(Mayo2005:风险比[HR] = 5.43,95%置信区间[95%CI]1.21-24.39,p = 0.027;瑞典 2014:HR = 13.02,95%CI 5.25-32.28,p < 0.001;NCI2019:HR = 5.85,95%CI 2.49-13.74,p < 0.001)。我们的研究表明,MGUS 风险分层模型可以纵向应用于反复确定和改善个体进展风险。在随访期间,患者向更高风险类别转移应促使在临床常规中更频繁地监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdb/11349746/a4b4e9af0258/41408_2024_1126_Fig1_HTML.jpg

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