Predicting the Progression from Asymptomatic to Symptomatic Multiple Myeloma and Stage Classification Using Gene Expression Data.

IF 4.4 2区 医学 Q1 ONCOLOGY Cancers Pub Date : 2025-01-20 DOI:10.3390/cancers17020332
Nestoras Karathanasis, George M Spyrou
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Abstract

Background: The accurate staging of multiple myeloma (MM) is essential for optimizing treatment strategies, while predicting the progression of asymptomatic patients, also referred to as monoclonal gammopathy of undetermined significance (MGUS), to symptomatic MM remains a significant challenge due to limited data. This study aimed to develop machine learning models to enhance MM staging accuracy and stratify asymptomatic patients by their risk of progression.

Methods: We utilized gene expression microarray datasets to develop machine learning models, combined with various data transformations. For multiple myeloma staging, models were trained on a single dataset and validated across five independent datasets, with performance evaluated using multiclass area under the curve (AUC) metrics. To predict progression in asymptomatic patients, we employed two approaches: (1) training models on a dataset comprising asymptomatic patients who either progressed or remained stable without progressing to multiple myeloma, and (2) training models on multiple datasets combining asymptomatic and multiple myeloma samples and then testing their ability to distinguish between asymptomatic and asymptomatic that progressed. We performed feature selection and enrichment analyses to identify key signaling pathways underlying disease stages and progression.

Results: Multiple myeloma staging models demonstrated high efficacy, with ElasticNet achieving consistent multiclass AUC values of 0.9 across datasets and transformations, demonstrating robust generalizability. For asymptomatic progression, both modeling approaches yielded similar results, with AUC values exceeding 0.8 across datasets and algorithms (ElasticNet, Boosting, and Support Vector Machines), underscoring their potential in identifying progression risk. Enrichment analyses revealed key pathways, including PI3K-Akt, MAPK, Wnt, and mTOR, as central to MM pathogenesis.

Conclusions: To the best of our knowledge, this is the first study to utilize gene expression datasets for classifying patients across different stages of multiple myeloma and to integrate multiple myeloma with asymptomatic cases to predict disease progression, offering a novel methodology with potential clinical applications in patient monitoring and early intervention.

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利用基因表达数据预测多发性骨髓瘤从无症状到有症状的进展及分期
背景:多发性骨髓瘤(MM)的准确分期对于优化治疗策略至关重要,而由于数据有限,预测无症状患者(也称为未确定意义的单克隆γ病(MGUS))向症状性MM的进展仍然是一个重大挑战。本研究旨在开发机器学习模型,以提高MM分期准确性,并根据进展风险对无症状患者进行分层。方法:利用基因表达微阵列数据集开发机器学习模型,并结合各种数据转换。对于多发性骨髓瘤分期,模型在单个数据集上进行训练,并在五个独立数据集上进行验证,使用多类别曲线下面积(AUC)指标评估性能。为了预测无症状患者的进展,我们采用了两种方法:(1)在包含进展或保持稳定但未进展为多发性骨髓瘤的无症状患者的数据集上训练模型,以及(2)在包含无症状和多发性骨髓瘤样本的多个数据集上训练模型,然后测试它们区分无症状和无症状进展的能力。我们进行了特征选择和富集分析,以确定疾病分期和进展的关键信号通路。结果:多发性骨髓瘤分期模型显示出很高的疗效,ElasticNet在数据集和转换中实现了一致的多类别AUC值0.9,显示出强大的泛化能力。对于无症状进展,两种建模方法产生了相似的结果,在数据集和算法(ElasticNet、Boosting和支持向量机)中,AUC值都超过0.8,强调了它们在识别进展风险方面的潜力。富集分析揭示了关键通路,包括PI3K-Akt、MAPK、Wnt和mTOR,是MM发病机制的核心。结论:据我们所知,这是第一个利用基因表达数据集对不同阶段多发性骨髓瘤患者进行分类,并将多发性骨髓瘤与无症状病例结合起来预测疾病进展的研究,为患者监测和早期干预提供了一种具有潜在临床应用价值的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancers
Cancers Medicine-Oncology
CiteScore
8.00
自引率
9.60%
发文量
5371
审稿时长
18.07 days
期刊介绍: Cancers (ISSN 2072-6694) is an international, peer-reviewed open access journal on oncology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
期刊最新文献
Correction: Berezowski et al. Biomarkers in Renal Cell Carcinoma: A Systematic Review and Immunohistochemical Validation Study. Cancers 2025, 17, 2588. RETRACTED: Li et al. TRIM10 Is Downregulated in Acute Myeloid Leukemia and Plays a Tumor Suppressive Role via Regulating NF-κB Pathway. Cancers 2023, 15, 417. Diagnostic Utility of Endoscopic Features and Endoscopic Ultrasonography for Ulcerative Colitis-Associated Neoplasia: A Retrospective Study on the Role of Endoscopic Submucosal Dissection as a Total Biopsy. Commentary on "Shifting Paradigm: Utilization and Outcomes with Neoadjuvant Chemotherapy for cT4 and cN2 Colon Cancers". Correction: Chitoran et al. A Systematic Review and Meta-Analysis on Opioid Management of Dyspnea in Cancer Patients. Cancers 2025, 17, 1368.
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