Automatic classification and segmentation of blast cells using deep transfer learning and active contours

IF 2.2 4区 医学 Q3 HEMATOLOGY International Journal of Laboratory Hematology Pub Date : 2024-05-10 DOI:10.1111/ijlh.14305
Divine Senanu Ametefe, Suzi Seroja Sarnin, Darmawaty Mohd Ali, George Dzorgbenya Ametefe, Dah John, Abdulmalik Adozuka Aliu, Zadok Zoreno
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Abstract

Introduction

Acute lymphoblastic leukemia (ALL) presents a formidable challenge in hematological malignancies, necessitating swift and precise diagnostic techniques for effective intervention. The conventional manual microscopy of blood smears, although widely practiced, suffers from significant limitations including labor-intensity and susceptibility to human error, particularly in distinguishing the subtle differences between normal and leukemic cells.

Methods

To overcome these limitations, our research introduces the ALLDet classifier, an innovative tool employing deep transfer learning for the automated analysis and categorization of ALL from White Blood Cell (WBC) nuclei images. Our investigation encompassed the evaluation of nine state-of-the-art pre-trained convolutional neural network (CNN) models, namely VGG16, VGG19, ResNet50, ResNet101, DenseNet121, DenseNet201, Xception, MobileNet, and EfficientNetB3. We augmented this approach by incorporating a sophisticated contour-based segmentation technique, derived from the Chan-Vese model, aimed at the meticulous segmentation of blast cell nuclei in blood smear images, thereby enhancing the accuracy of our analysis.

Results

The empirical assessment of these methodologies underscored the superior performance of the EfficientNetB3 model, which demonstrated exceptional metrics: a recall specificity of 98.5%, precision of 95.86%, F1-score of 97.16%, and an overall accuracy rate of 97.13%. The Chan-Vese model's adaptability to the irregular shapes of blast cells and its noise-resistant segmentation capability were key to capturing the complex morphological changes essential for accurate segmentation.

Conclusion

The combined application of the ALLDet classifier, powered by EfficientNetB3, with our advanced segmentation approach, emerges as a formidable advancement in the early detection and accurate diagnosis of ALL. This breakthrough not only signifies a pivotal leap in leukemia diagnostic methodologies but also holds the promise of significantly elevating the standards of patient care through the provision of timely and precise diagnoses. The implications of this study extend beyond immediate clinical utility, paving the way for future research to further refine and enhance the capabilities of artificial intelligence in medical diagnostics.

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利用深度迁移学习和主动轮廓对爆炸细胞进行自动分类和分割。
导言:急性淋巴细胞白血病(ALL)是血液恶性肿瘤中的一项严峻挑战,需要快速、精确的诊断技术才能进行有效干预。传统的手工显微镜检查血液涂片的方法虽然被广泛使用,但存在很大的局限性,包括劳动强度大、容易出现人为错误,尤其是在区分正常细胞和白血病细胞的细微差别方面:为了克服这些局限性,我们的研究引入了 ALLDet 分类器,这是一种采用深度迁移学习的创新工具,可自动分析白细胞(WBC)核图像并对 ALL 进行分类。我们的研究包括评估九种最先进的预训练卷积神经网络(CNN)模型,即 VGG16、VGG19、ResNet50、ResNet101、DenseNet121、DenseNet201、Xception、MobileNet 和 EfficientNetB3。我们在这一方法的基础上,加入了源自 Chan-Vese 模型的复杂轮廓分割技术,旨在对血液涂片图像中的爆炸细胞核进行细致分割,从而提高分析的准确性:对这些方法进行的实证评估凸显了 EfficientNetB3 模型的卓越性能,该模型的指标非常出色:召回特异性为 98.5%,精确度为 95.86%,F1 分数为 97.16%,总体准确率为 97.13%。Chan-Vese 模型对爆炸细胞不规则形状的适应性及其抗噪分割能力是捕捉复杂形态变化的关键,而复杂形态变化对准确分割至关重要:由 EfficientNetB3 支持的 ALLDet 分类器与我们先进的分割方法的结合应用,在 ALL 的早期检测和准确诊断方面取得了巨大进步。这一突破不仅标志着白血病诊断方法的关键性飞跃,而且有望通过提供及时准确的诊断大大提高患者护理标准。这项研究的意义不仅限于直接的临床应用,它还为未来的研究铺平了道路,以进一步完善和提高人工智能在医疗诊断方面的能力。
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来源期刊
CiteScore
4.50
自引率
6.70%
发文量
211
审稿时长
6-12 weeks
期刊介绍: The International Journal of Laboratory Hematology provides a forum for the communication of new developments, research topics and the practice of laboratory haematology. The journal publishes invited reviews, full length original articles, and correspondence. The International Journal of Laboratory Hematology is the official journal of the International Society for Laboratory Hematology, which addresses the following sub-disciplines: cellular analysis, flow cytometry, haemostasis and thrombosis, molecular diagnostics, haematology informatics, haemoglobinopathies, point of care testing, standards and guidelines. The journal was launched in 2006 as the successor to Clinical and Laboratory Hematology, which was first published in 1979. An active and positive editorial policy ensures that work of a high scientific standard is reported, in order to bridge the gap between practical and academic aspects of laboratory haematology.
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