{"title":"A Deep Learning Model for IMMP-Based Residual Disease Monitoring in AML with Monocytic Differentiation.","authors":"Jing Ding, Huiying Qiu, Chunling Zhang, Weilin Liu, Xinyi Jin, Ting Xu, Zongyue Lu, Jiatao Lou, Huidan Li","doi":"10.3390/diagnostics16081244","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Acute myeloid leukemia (AML) with monocytic differentiation poses significant clinical challenges, including high relapse rates and chemotherapy resistance. Current morphological assessment is limited by inter-observer variability, low sensitivity, and inefficiency, especially for detecting low-level residual disease. This creates an urgent need for automated, objective tools to improve diagnostic consistency and monitoring. Artificial intelligence, particularly deep learning, offers potential for extracting high-dimensional cytomorphological features to address these gaps. <b>Methods:</b> A retrospective cohort of 184 bone marrow smear slides from patients with monocytic leukemia was used. The core biomarker was the immature monocyte percentage (IMMP), defined as monoblasts plus promonocytes among nucleated cells, with a 2.0% clinical cutoff. An EfficientNet-based convolutional neural network was developed via transfer learning and trained to classify four cell types: monoblasts, promonocytes, monocytes, and other cells. <b>Results:</b> The model achieved robust cell-level classification, with F1 scores of 0.82 for monoblasts and 0.34 for promonocytes. At the slide level, using an optimized IMMP threshold of 0.045, it accurately assessed persistent leukemic cell burden with 78.9% <i>Accuracy</i>, 81.1% <i>Recall</i>, and 76.9% <i>Specificity</i>. Model-predicted IMMP values showed strong correlation with expert-derived values (Pearson r = 0.827), demonstrating reliable quantitative agreement. <b>Conclusions:</b> This deep learning model provides an automated, objective tool for quantifying immature monocytes, addressing key limitations in morphological assessment of monocytic AML. The IMMP metric shows promise for monitoring treatment response, predicting relapse, and potentially identifying patients at risk of venetoclax-based therapy resistance. While promising, prospective multicenter validation is needed to translate these findings into routine clinical practice.</p>","PeriodicalId":11225,"journal":{"name":"Diagnostics","volume":"16 8","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13115004/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/diagnostics16081244","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Acute myeloid leukemia (AML) with monocytic differentiation poses significant clinical challenges, including high relapse rates and chemotherapy resistance. Current morphological assessment is limited by inter-observer variability, low sensitivity, and inefficiency, especially for detecting low-level residual disease. This creates an urgent need for automated, objective tools to improve diagnostic consistency and monitoring. Artificial intelligence, particularly deep learning, offers potential for extracting high-dimensional cytomorphological features to address these gaps. Methods: A retrospective cohort of 184 bone marrow smear slides from patients with monocytic leukemia was used. The core biomarker was the immature monocyte percentage (IMMP), defined as monoblasts plus promonocytes among nucleated cells, with a 2.0% clinical cutoff. An EfficientNet-based convolutional neural network was developed via transfer learning and trained to classify four cell types: monoblasts, promonocytes, monocytes, and other cells. Results: The model achieved robust cell-level classification, with F1 scores of 0.82 for monoblasts and 0.34 for promonocytes. At the slide level, using an optimized IMMP threshold of 0.045, it accurately assessed persistent leukemic cell burden with 78.9% Accuracy, 81.1% Recall, and 76.9% Specificity. Model-predicted IMMP values showed strong correlation with expert-derived values (Pearson r = 0.827), demonstrating reliable quantitative agreement. Conclusions: This deep learning model provides an automated, objective tool for quantifying immature monocytes, addressing key limitations in morphological assessment of monocytic AML. The IMMP metric shows promise for monitoring treatment response, predicting relapse, and potentially identifying patients at risk of venetoclax-based therapy resistance. While promising, prospective multicenter validation is needed to translate these findings into routine clinical practice.
背景:单核细胞分化的急性髓性白血病(AML)具有显著的临床挑战,包括高复发率和化疗耐药。目前的形态学评估受到观察者间可变性、低灵敏度和低效率的限制,特别是在检测低水平残留疾病时。这就迫切需要自动化、客观的工具来提高诊断一致性和监测。人工智能,特别是深度学习,提供了提取高维细胞形态学特征的潜力,以解决这些空白。方法:对184例单核细胞白血病患者骨髓涂片进行回顾性分析。核心生物标志物是未成熟单核细胞百分比(IMMP),定义为单核细胞加上有核细胞中的前单核细胞,临床临界值为2.0%。通过迁移学习开发了一个基于efficientnet的卷积神经网络,并训练其对四种细胞类型进行分类:单核细胞、单核细胞、单核细胞和其他细胞。结果:该模型实现了稳健的细胞水平分类,单核细胞F1得分为0.82,单核细胞F1得分为0.34。在载片水平,使用优化的IMMP阈值0.045,它准确地评估了持续白血病细胞负荷,准确率为78.9%,召回率为81.1%,特异性为76.9%。模型预测的IMMP值与专家推导值有很强的相关性(Pearson r = 0.827),证明了可靠的定量一致性。结论:该深度学习模型为量化未成熟单核细胞提供了一种自动化、客观的工具,解决了单核细胞AML形态学评估的关键限制。IMMP指标有望监测治疗反应,预测复发,并潜在地识别有venetoclax基础治疗耐药风险的患者。虽然有希望,但需要前瞻性多中心验证才能将这些发现转化为常规临床实践。
DiagnosticsBiochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍:
Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.