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Modelling and validation of a 6 MV compact linear accelerator via Monte Carlo simulation using Geant4 Application for Tomographic Emission (GATE). 基于Geant4应用于断层发射(GATE)的6 MV紧凑型直线加速器的蒙特卡罗仿真建模与验证。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-30 DOI: 10.1088/2057-1976/ada9ef
Maynard E Limbaco, Franklin U Toledo, Renna Mae V Tondo, Salasa A Nawang

Objective. To accurately model and validate the 6 MV Elekta Compact linear accelerator using the Geant4 Application for Tomographic Emission (GATE). In particular, this study focuses on the precise calibration and validation of critical parameters, including jaw collimator positioning, electron source nominal energy, flattening filter geometry, and electron source spot size, which are often not provided in technical documentation.Methods. Simulation of the Elekta CompactTM6 MV linear accelerator was performed using the Geant4 Application for Tomographic Emission (GATE) v.9.1. A 50 cm × 50 cm × 50 cm water phantom was irradiated with a source-to-surface distance of 100 cm. Percentage Depth Dose Profile (PDD) and Lateral Dose Profile (Crossplane and Inplane) were assessed as reference dose measurements. The half-length field difference (FHLD) method was introduced to optimize the jaw collimator setup. Gamma index analysis was used to quantitatively assess the accuracy of the simulated dosimetry data in relation to the actual dose measurements.Results. Crucial parameters of the Linac Head have been successfully optimized. The validation achieved Gamma-Index acceptance rates of 97.93% for the Depth Dose profile, 100% for the Crossplane (X) Dose Profile, and 93.98% for the Inplane (Y) Dose Profile, all meeting the 1%/1 mm Gamma-Index criteria.Conclusion. The simulation and calibration of the Elekta Compact Linac have achieved a reliable model with high fidelity in dosimetry calculations which could pave the way for the future development and application of new techniques using Elekta CompactTMLinear Accelerator.

目的:利用Geant4应用层析发射(GATE)对6 MV Elekta compacttm直线加速器进行精确建模和验证。特别地,本研究侧重于关键参数的精确校准和验证,包括颚准直器定位,电子源标称能量,平坦滤波器几何形状和电子源光斑尺寸,这些通常没有在技术文档中提供。 ;方法:使用Geant4应用程序断层发射(GATE) v.9.1对Elekta CompactTM6 MV线性加速器进行仿真。一个50 cm × 50 cm × 50 cm的水影以源-表面距离100 cm照射。百分比深度剂量分布图(PDD)和横向剂量分布图(横切面和内平面)作为参考剂量测量进行评估。采用半长视场差法对颚式准直器的设置进行了优化。采用Gamma指数分析定量评估模拟剂量学数据与实际剂量测量值的准确性。结果:成功优化了直线磁头的关键参数。验证后,深度剂量谱的γ -指数接受率为97.93%,横面(X)剂量谱为100%,内面(Y)剂量谱为93.98%,均满足1%/1mm的γ -指数标准。通过对Elekta CompactTMLinac的仿真和校准,获得了一个可靠的、具有高保真度的剂量学计算模型,为未来使用Elekta CompactTMLinear Accelerator开发和应用新技术铺平了道路。
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引用次数: 0
Hybrid data augmentation strategies for robust deep learning classification of corneal topographic maptopographic map. 角膜地形图鲁棒深度学习分类的混合数据增强策略。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-30 DOI: 10.1088/2057-1976/adabea
Abir Chaari, Imen Fourati Kallel, Sonda Kammoun, Mondher Frikha

Deep learning has emerged as a powerful tool in medical imaging, particularly for corneal topographic map classification. However, the scarcity of labeled data poses a significant challenge to achieving robust performance. This study investigates the impact of various data augmentation strategies on enhancing the performance of a customized convolutional neural network model for corneal topographic map classification. We propose a hybrid data augmentation approach that combines traditional transformations, generative adversarial networks, and specific generative models. Experimental results demonstrate that the hybrid data augmentation method, achieves the highest accuracy of 99.54%, significantly outperforming individual data augmentation techniques. This hybrid approach not only improves model accuracy but also mitigates overfitting issues, making it a promising solution for medical image classification tasks with limited data availability.

深度学习已经成为医学成像,特别是角膜地形图分类的强大工具。然而,标记数据的稀缺性对实现稳健性能提出了重大挑战。本研究探讨了不同的数据增强策略对增强自定义卷积神经网络角膜地形图分类模型性能的影响。我们提出了一种混合数据增强方法,该方法结合了传统转换、生成对抗网络和特定生成模型。实验结果表明,混合数据增强方法的准确率高达99.54%,显著优于单个数据增强方法。这种混合方法不仅提高了模型精度,而且减轻了过拟合问题,使其成为数据可用性有限的医学图像分类任务的一个有希望的解决方案。
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引用次数: 0
A novel approach in cancer diagnosis: integrating holography microscopic medical imaging and deep learning techniques-challenges and future trends. 癌症诊断的新方法:整合全息显微医学成像和深度学习技术-挑战和未来趋势。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-29 DOI: 10.1088/2057-1976/ad9eb7
Asifa Nazir, Ahsan Hussain, Mandeep Singh, Assif Assad

Medical imaging is pivotal in early disease diagnosis, providing essential insights that enable timely and accurate detection of health anomalies. Traditional imaging techniques, such as Magnetic Resonance Imaging (MRI), Computer Tomography (CT), ultrasound, and Positron Emission Tomography (PET), offer vital insights into three-dimensional structures but frequently fall short of delivering a comprehensive and detailed anatomical analysis, capturing only amplitude details. Three-dimensional holography microscopic medical imaging provides a promising solution by capturing the amplitude (brightness) and phase (structural information) details of biological structures. In this study, we investigate the novel collaborative potential of Deep Learning (DL) and holography microscopic phase imaging for cancer diagnosis. The study comprehensively examines existing literature, analyzes advancements, identifies research gaps, and proposes future research directions in cancer diagnosis through the integrated Quantitative Phase Imaging (QPI) and DL methodology. This novel approach addresses a critical limitation of traditional imaging by capturing detailed structural information, paving the way for more accurate diagnostics. The proposed approach comprises tissue sample collection, holographic image scanning, preprocessing in case of imbalanced datasets, and training on annotated datasets using DL architectures like U-Net and Vision Transformer(ViT's). Furthermore, sophisticated concepts in DL, like the incorporation of Explainable AI (XAI) techniques, are suggested for comprehensive disease diagnosis and identification. The study thoroughly investigates the advantages of integrating holography imaging and DL for precise cancer diagnosis. Additionally, meticulous insights are presented by identifying the challenges associated with this integration methodology.

医学成像在早期疾病诊断中至关重要,它提供了能够及时准确检测健康异常的基本见解。传统的成像技术,如磁共振成像(MRI)、计算机断层扫描(CT)、超声波和正电子发射断层扫描(PET),提供了对三维结构的重要见解,但往往无法提供全面和详细的解剖分析,只能捕获振幅细节。三维全息显微医学成像通过捕获生物结构的振幅(亮度)和相位(结构信息)细节提供了一个有前途的解决方案。在这项研究中,我们探讨了深度学习(DL)和全息显微相位成像在癌症诊断中的新型协作潜力。本研究通过综合定量相位成像(QPI)和DL方法对现有文献进行了全面的研究,分析了研究进展,确定了研究差距,并提出了癌症诊断的未来研究方向。这种新方法通过捕获详细的结构信息,解决了传统成像的一个关键限制,为更准确的诊断铺平了道路。提出的方法包括组织样本收集、全息图像扫描、不平衡数据集的预处理,以及使用U-Net和Vision Transformer(ViT)等DL架构对带注释的数据集进行训练。此外,DL中的复杂概念,如可解释人工智能技术(XAI)的结合,被建议用于全面的疾病诊断和识别。本研究深入探讨了全息成像与深度影像相结合在肿瘤精确诊断中的优势。此外,通过识别与此集成方法相关的挑战,提供了细致的见解。
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引用次数: 0
Biological cell response to electric field: a review of equivalent circuit models and future challenges. 生物细胞对电场的反应:等效电路模型回顾与未来挑战
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-24 DOI: 10.1088/2057-1976/ad8092
MirHojjat Seyedi

Biological cells, characterized by complex and dynamic structures, demand precise models for comprehensive understanding, especially when subjected to external factors such as electric fields (EF) for manipulation or treatment. This interaction is integral to technologies like pulsed electric fields (PEF), inducing reversible and irreversible structural variations. Our study explores both simplified and sophisticated equivalent circuit models for biological cells under the influence of an external EF, covering diverse cell structures from single- to double-shell configurations. The paper highlights challenges in circuit modeling, specifically addressing the incorporation of reversible or irreversible pores in the membrane during external EF interactions, emphasizing the need for further research to refine technical aspects in this field. Additionally, we review a comparative analysis of the performance and applicability of the proposed circuit models, providing insights into their strengths and limitations. This contributes to a deeper insight of the complexities associated with modeling biological cells under external EF influences, paving the way for enhanced applications in medical and technological domains in future.

生物细胞具有复杂而动态的结构,需要精确的模型来全面了解,尤其是在受到电场(EF)等外部因素操纵或治疗时。这种相互作用是脉冲电场(PEF)等技术不可或缺的一部分,会引起可逆和不可逆的结构变化。我们的研究探讨了外部电场影响下生物细胞的简化和复杂等效电路模型,涵盖了从单壳到双壳配置的各种细胞结构。论文强调了电路建模面临的挑战,特别是在外部 EF 相互作用时在膜中加入可逆或不可逆孔的问题,强调了进一步研究以完善该领域技术方面的必要性。此外,我们还对所提出的电路模型的性能和适用性进行了比较分析,深入了解了这些模型的优势和局限性。这有助于更深入地了解与外部 EF 影响下的生物细胞建模相关的复杂性,为今后加强在医疗和技术领域的应用铺平道路。
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引用次数: 0
Determining event-related desynchronization onset latency of foot dorsiflexion in people with multiple sclerosis using the cluster depth tests. 使用聚类深度试验确定多发性硬化症患者足背屈的事件相关非同步发作潜伏期
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-24 DOI: 10.1088/2057-1976/adaaf8
L Carolina Carrere, Julián Furios, José A Biurrun Manresa, Carlos H Ballario, Carolina B Tabernig

Multiple sclerosis (MS) is a disorder in which the body's immune system attacks structures of the central nervous system, resulting in lesions that can occur throughout the brain and spinal cord. Cortical lesions, in particular, can contribute to motor dysfunction. Walking disability is reported as the main impairment by people with MS (pwMS), often due to limited ankle movement. This study explored the event-related desynchronization (ERD) onset latency of the sensorimotor rhythms during foot dorsiflexion in pwMS computed using an objective and independent of human criterion method, as an electroencephalogram (EEG) based biomarker. EEG signals were recorded in eight persons with neither neurological condition nor motor dysfunction and eight pwMS with relapsing-remitting, primary progressive or secondary progressive MS. Recordings were divided into three groups: control, more affected lower limb and less affected lower limb. The ERD-onset latency was determined using a method based on the percent of ERD time course and the cluster depth tests. The median and interquartile range of the ERD-onset latency were 1186.0 (1100.0, 1250.0) ms; 1064.0 (1031.0, 1127.0) ms for the more and less affected groups respectively, whereas the median and interquartile range for the control group was 656.0 (472.2, 950.0) ms. There was a significant delay in the ERD-onset latencies of the pwMS groups compared to the control group (p<0.001 for both comparisons). These findings suggest that the ERD-onset latency computed using the proposed method could be used as an EEG biomarker to evaluate disease progression or therapeutic interventions in pwMS.

多发性硬化症(MS)是一种身体免疫系统攻击中枢神经系统结构的疾病,导致整个大脑和脊髓出现病变。尤其是皮质损伤,可导致运动功能障碍。据报道,行走障碍是多发性硬化症(pwMS)患者的主要损害,通常是由于踝关节活动受限。本研究探讨了pwMS中足背屈过程中感觉运动节律的事件相关去同步(ERD)发作潜伏期,该潜伏期采用客观且独立于人类标准的方法计算,作为基于脑电图(EEG)的生物标志物。记录8名无神经系统疾病或运动功能障碍患者的脑电图信号,以及8名复发缓解型、原发性进行性或继发性进行性ms患者的脑电图信号。记录分为三组:对照组、较重下肢和较轻下肢。使用基于ERD时间过程百分比和聚类深度测试的方法确定ERD发作延迟。erd发病潜伏期中位数和四分位数范围分别为1186.0 (1100.0,1250.0)ms;而对照组的中位数和四分位数范围为656.0 (472.2,950.0)ms。与对照组相比,pwMS组的erd发作潜伏期明显延迟(p . 1)
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引用次数: 0
A novel hollow-core antiresonant fiber-based biosensor for blood component detection in the THz regime. 一种用于太赫兹区血液成分检测的新型空心抗谐振纤维生物传感器。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-24 DOI: 10.1088/2057-1976/ada88a
Maharaja Balaji, Sathiyan Samikannu

This article proposes a novel biosensor based on a five-semi-circular cladding tube hollow core antiresonant fiber (HC-ARF) with a frequency range of 0.5-2.8 THz, using Zeonex as the background material. The HC-ARF biosensor analyses various blood components, namely water, plasma, white blood cells (WBC), hemoglobin (HB), and red blood cells (RBC). We utilized COMSOL Multiphysics to perform the numerical analysis of the sensor model. For water, plasma, WBC, HB, and RBC, the proposed HC-ARF biosensor exhibits the highest sensitivity levels of 99.50%, 99.58%, 99.43%, 99.58%, and 99.46%, respectively. Furthermore, it demonstrates confinement loss (CL) and effective material loss (EML) of 1.3  × 10-3dBcm-1and 5.3  × 10-5dBcm-1, respectively.

本文以Zeonex为背景材料,提出了一种基于五半圆包层管空心抗谐振光纤(HC-ARF)的新型生物传感器,其频率范围为0.5 ~ 2.8太赫兹。HC-ARF生物传感器分析各种血液成分,即水、血浆、白细胞(WBC)、血红蛋白(HB)和红细胞(RBC)。我们利用COMSOL Multiphysics对传感器模型进行数值分析。对于水、血浆、白细胞、血红蛋白和红细胞,所提出的hc - arf生物传感器灵敏度最高,分别为99.50%、99.58%、99.43%、99.58%和99.46%。此外,它还表明约束损耗(CL)和有效材料损耗(EML)分别为1.3 ×10-3 dBcm-1和5.3 ×10-5 dBcm-1。
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引用次数: 0
Simulations of the potential for diffraction enhanced imaging at 8 kev using polycapillary optics. 用多毛细光学模拟8kev衍射增强成像的潜力。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-24 DOI: 10.1088/2057-1976/ada9ed
Carmen A Bittel, Carolyn A MacDonald

Conventional x-ray radiography relies on attenuation differences in the object, which often results in poor contrast in soft tissues. X-ray phase imaging has the potential to produce higher contrast but can be difficult to utilize. Instead of grating-based techniques, analyzer-based imaging, also known as diffraction enhanced imaging (DEI), uses a monochromator crystal with an analyzer crystal after the object. Analyzer-based systems most commonly employ synchrotron sources to provide adequate intensity, and typically use higher photon energies. In this work, a simulation has been devised to assess the potential for a polycapillary-based system. A polycapillary collimating optic has previously been shown to greatly enhance the intensity of the beam diffracted from the monochromatizing crystal. Detailed simulation of the optic is computationally intensive and requires comprehensive knowledge of the internal shape of the optic, so a simple geometric model using easier to obtain optic output data was developed and compared to the more detailed simulation. After verification, refraction band visibility was used as a quality parameter to address the effectiveness of the polycapillary-based DEI system at x-ray photon energies of 8 and 17.5 keV. The result shows promise for a polycapillary-coupled analyzer-based system even at low x-ray photon energy.

传统的x射线摄影依赖于物体的衰减差异,这通常导致软组织的对比度较差。x射线相位成像有可能产生更高的对比度,但很难利用。与基于光栅的技术不同,基于分析仪的成像,也称为衍射增强成像(DEI),使用的是单色器晶体和物体后的分析仪晶体。基于分析仪的系统通常采用同步加速器源来提供足够的强度,并且通常使用更高的光子能量。在这项工作中,已经设计了一个模拟来评估基于多毛细血管的系统的潜力。准直光学先前已被证明可以大大增强单色化晶体衍射光束的强度。光学元件的详细仿真计算量大,需要全面了解光学元件的内部形状,因此开发了一个简单的几何模型,使用更容易获得光学输出数据,并与更详细的仿真进行了比较。在验证后,以折射波段可见性作为质量参数来评价基于多毛细管的DEI系统在x射线光子能量为8和17.5 keV时的有效性。结果表明,即使在低x射线光子能量下,基于多毛细管耦合分析仪的系统也是有希望的。
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引用次数: 0
Multimodal multiview bilinear graph convolutional network for mild cognitive impairment diagnosis. 多模态多视图双线性图卷积网络在轻度认知障碍诊断中的应用。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-22 DOI: 10.1088/2057-1976/ada8af
Guanghui Wu, Xiang Li, Yunfeng Xu, Benzheng Wei

Mild cognitive impairment (MCI) is a significant predictor of the early progression of Alzheimer's disease (AD) and can serve as an important indicator of disease progression. However, many existing methods focus mainly on the image when processing brain imaging data, ignoring other non-imaging data (e.g., genetic, clinical information, etc.) that may have underlying disease information. In addition, imaging data acquired from different devices may exhibit varying degrees of heterogeneity, potentially resulting in numerous noisy connections during network construction. To address these challenges, this study proposes a Multimodal Multiview Bilinear Graph Convolution (MMBGCN) framework for disease risk prediction. Firstly, grey matter (GM), white matter (WM) and cerebrospinal fluid (CSF) features are extracted from magnetic resonance imaging (MRI), and non-imaging information is combined with the features extracted from MRI to construct a multimodal shared adjacency matrix. The shared adjacency matrix is then used to construct the multiview network so that the effect of potential disease information in the non-imaging information on the model can be considered. Finally, the MRI features extracted by the multiview network are weighted to reduce noise, and then the spatial pattern is restored by bilinear convolution. The features of the recovered spatial patterns are then combined with the genetic information for disease prediction. The proposed method is tested on the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset. Extensive experiments demonstrate the superior performance of the proposed framework and its ability to outperform other related algorithms. The average classification accuracy in the binary classification task in this study is 89.6%. The experimental results demonstrate that the method proposed in this study facilitates research on MCI diagnosis using multimodal data.

轻度认知障碍(Mild cognitive impairment, MCI)是阿尔茨海默病早期进展的重要预测因子,可作为疾病进展的重要指标。然而,现有的许多方法在处理脑成像数据时主要关注图像本身,而忽略了其他可能具有潜在疾病信息的非成像数据(如遗传、临床信息等)。此外,从不同设备获取的成像数据可能表现出不同程度的异质性,这可能导致网络构建过程中出现大量噪声连接。为了解决这些挑战,本研究提出了一种用于疾病风险预测的多模态多视图双线性图卷积(MMBGCN)框架。首先从磁共振成像(MRI)中提取灰质(GM)、白质(WM)和脑脊液(CSF)特征,并将非成像信息与MRI提取的特征相结合,构建多模态共享邻接矩阵;然后利用共享邻接矩阵构建多视图网络,以考虑非成像信息中潜在疾病信息对模型的影响。最后,对多视点网络提取的MRI特征进行加权去噪,然后通过双线性卷积恢复空间格局。然后将恢复的空间模式的特征与疾病预测的遗传信息相结合。该方法在阿尔茨海默病神经成像倡议(ADNI)数据集上进行了测试。大量的实验证明了该框架的优越性能和优于其他相关算法的能力。本研究中二元分类任务的平均分类准确率为89.6%。实验结果表明,本文提出的方法为基于多模态数据的MCI诊断研究提供了便利。
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引用次数: 0
Reconstruction of local three-dimensional temperature field of tumor cells with low-toxic nanoscale quantum-dot thermometer and cepstrum spatial localization algorithm. 低毒纳米量子点温度计和倒谱空间定位算法重建肿瘤细胞局部三维温度场。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-22 DOI: 10.1088/2057-1976/ada9ee
Jun Yang, Lingyu Huang, HanLiang Du, Lei Zhang, Ben Q Li, Mutian Xu

The optimal method for three-dimensional thermal imaging within cells involves collecting intracellular temperature responses while simultaneously obtaining corresponding 3D positional information. Current temperature measurement techniques based on the photothermal properties of quantum dots face several limitations, including high cytotoxicity and low fluorescence quantum yields. These issues affect the normal metabolic processes of tumor cells. This study synthesizes a low-toxicity cell membrane-targeted quantum dot temperature sensor by optimizing the synthesis method of CdTe/CdS/ZnS core-shell structured quantum dots. Compared to CdTe-targeted quantum dot temperature sensors, the cytotoxicity of CdTe/CdS/ZnS-targeted quantum dot temperature sensors is reduced by 40.79%. Additionally, a novel cepstrum-based spatial localization algorithm is proposed to achieve rapidly compute the three-dimensional positions of densely distributed quantum dot temperature sensors. Ultimately, both targeted and non-targeted CdTe/CdS/ZnS quantum dot temperature sensors were used simultaneously to label the internal and external regions of human osteosarcoma cells to obtain temperature data at these labeling positions. By combining this with the cepstrum-based spatial localization algorithm, the spatial coordinates of the quantum dot temperature sensors were obtained. Three-dimensional temperature field reconstruction of three local regions was achieved within a 12 μm axial range in living cells. The method described in this paper can be widely applied to the quantitative study of intracellular thermal responses.

细胞内三维热成像的最佳方法是收集细胞内温度响应,同时获得相应的三维位置信息。目前基于量子点光热特性的温度测量技术面临着一些限制,包括高细胞毒性和低荧光量子产率。这些问题影响肿瘤细胞的正常代谢过程。本研究通过优化CdTe/CdS/ZnS核壳结构量子点的合成方法,合成了一种低毒性的细胞膜靶向量子点温度传感器。与CdTe靶向量子点温度传感器相比,CdTe/CdS/ zns靶向量子点温度传感器的细胞毒性降低了40.79%。此外,提出了一种新的基于倒谱的空间定位算法,实现了密集分布量子点温度传感器三维位置的快速计算。最后,同时使用靶向和非靶向CdTe/CdS/ZnS量子点温度传感器对人骨肉瘤细胞的内部和外部区域进行标记,获得这些标记位置的温度数据。将该方法与基于倒谱的空间定位算法相结合,得到了量子点温度传感器的空间坐标。在活细胞的轴向12 μm范围内实现了三个局部区域的三维温度场重建。该方法可广泛应用于细胞内热反应的定量研究。
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引用次数: 0
GradeDiff-IM: an ensembles model-based grade classification of breast cancer. gradiff - im:基于集成模型的乳腺癌分级。
IF 1.3 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-01-22 DOI: 10.1088/2057-1976/ada8ae
Sweta Manna, Sujoy Mistry, Keshav Dahal

Cancer grade classification is a challenging task identified from the cell structure of healthy and abnormal tissues. The practitioners learns about the malignant cell through the grading and plans the treatment strategy accordingly. A major portion of researchers used DL models for grade classification. However, the behavior of DL models is hidden type, it is unknown which features contribute to the accuracy and how the features are chosen for grading. To address the issue the study proposes a Grade Differentiation Integrated Model (GradeDiff-IM) to classify the grades G1, G2, and G3. In GradeDiff-IM, different ML models, are used for grade classification from clinical and pathological reports. The biological-significant features with ranking technique prioritize influential features are used to identify grades G. Subsequently, histopathological images are used by DL models for grade classification and compared with ML models. Instead of employing a single ML model, the GradeDiff-IM model uses the stack-ensembled approach to improve the grade G classification performance. The maximum accuracy is attained by stacking G1-98.2, G2-97.6, and G3-97.5. The proposed study shows that the ML ensemble model is more accurate than the DL models. As a result, the proposed model achieved higher accuracy for G by implementing the stacking technique than the other state-of-the-art models.

从健康组织和异常组织的细胞结构来确定癌症分级是一项具有挑战性的任务。分割者通过分级了解恶性细胞,并制定相应的治疗策略。大部分研究者使用深度学习模型进行等级分类。然而,深度学习模型的行为是隐藏型的,不知道哪些特征有助于准确性以及如何选择特征进行分级。为解决这一问题,本研究提出了等级分化积分法 ;模型(gradeff - im)对G1、G2、G3三个等级进行分类。在gradeff - im中,根据临床和病理报告使用不同的ML模型进行级别划分。采用生物显著性特征和排序技术对影响特征进行优先排序 ;随后,DL模型使用组织病理学图像进行级别分类,并与ML模型进行比较。gradiff - im模型没有使用单个ML模型,而是使用堆栈集成方法来改进grade ;G分类性能。通过叠加G1-98.2, G2-97.6和G3-97.5,可以获得最大的精度。研究表明,ML集成模型比DL模型更准确。结果表明,该模型具有较高的精度 ;对于G,通过实现叠加技术比其他最先进的模型。
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引用次数: 0
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