As machine learning (ML) continuously develops in cancer diagnosis and treatment, some researchers have attempted to predict the expression of programmed death ligand-1 (PD-L1) in non-small cell lung cancer (NSCLC) by ML. However, there is a lack of systematic evidence on the effectiveness of ML. We conducted a thorough search across Embase, PubMed, the Cochrane Library, and Web of Science from inception to December 14th, 2023.A systematic review and meta-analysis was conducted to assess the value of ML for predicting PD-L1 expression in NSCLC. Totally 30 studies with 12,898 NSCLC patients were included. The thresholds of PD-L1 expression level were < 1%, 1-49%, and ≥ 50%. In the validation set, in the binary classification for PD-L1 ≥ 1%, the pooled C-index was 0.646 (95%CI: 0.587-0.705), 0.799 (95%CI: 0.782-0.817), 0.806 (95%CI: 0.753-0.858), and 0.800 (95%CI: 0.717-0.883), respectively, for the clinical feature-, radiomics-, radiomics + clinical feature-, and pathomics-based ML models; in the binary classification for PD-L1 ≥ 50%, the pooled C-index was 0.649 (95%CI: 0.553-0.744), 0.771 (95%CI: 0.728-0.814), and 0.826 (95%CI: 0.783-0.869), respectively, for the clinical feature-, radiomics-, and radiomics + clinical feature-based ML models. At present, radiomics- or pathomics-based ML methods are applied for the prediction of PD-L1 expression in NSCLC, which both achieve satisfactory accuracy. In particular, the radiomics-based ML method seems to have wider clinical applicability as a non-invasive diagnostic tool. Both radiomics and pathomics serve as processing methods for medical images. In the future, we expect to develop medical image-based DL methods for intelligently predicting PD-L1 expression.

To evaluate the variability of fully automated airway quantitative CT (QCT) measures caused by different kernels and the effect of kernel conversion. This retrospective study included 96 patients who underwent non-enhanced chest CT at two centers. CT scans were reconstructed using four kernels (medium soft, medium sharp, sharp, very sharp) from three vendors. Kernel conversion targeting the medium soft kernel as reference was applied to sharp kernel images. Fully automated airway quantification was performed before and after conversion. The effects of kernel type and conversion on airway quantification were evaluated using analysis of variance, paired t-tests, and concordance correlation coefficient (CCC). Airway QCT measures (e.g., Pi10, wall thickness, wall area percentage, lumen diameter) decreased with sharper kernels (all, p < 0.001), with varying degrees of variability across variables and vendors. Kernel conversion substantially reduced variability between medium soft and sharp kernel images for vendors A (pooled CCC: 0.59 vs. 0.92) and B (0.40 vs. 0.91) and lung-dedicated sharp kernels of vendor C (0.26 vs. 0.71). However, it was ineffective for non-lung-dedicated sharp kernels of vendor C (0.81 vs. 0.43) and showed limited improvement in variability of QCT measures at the subsegmental level. Consistent airway segmentation and identical anatomic labeling improved subsegmental airway variability in theoretical tests. Deep learning-based kernel conversion reduced the measurement variability of airway QCT across various kernels and vendors but was less effective for non-lung-dedicated kernels and subsegmental airways. Consistent airway segmentation and precise anatomic labeling can further enhance reproducibility for reliable automated quantification. Question How do different CT reconstruction kernels affect the measurement variability of automated airway measurements, and can deep learning-based kernel conversion reduce this variability? Findings Kernel conversion improved measurement consistency across vendors for lung-dedicated kernels, but showed limited effectiveness for non-lung-dedicated kernels and subsegmental airways. Clinical relevance Understanding kernel-related variability in airway quantification and mitigating it through deep learning enables standardized analysis, but further refinements are needed for robust airway segmentation, particularly for improving measurement variability in subsegmental airways and specific kernels.

Current brain tumor segmentation methods often utilize a U-Net architecture based on efficient convolutional neural networks. While effective, these architectures primarily model local dependencies, lacking the ability to capture global interactions like pure Transformer. However, using pure Transformer directly causes the network to lose local feature information. To address this limitation, we propose the Generative Adversarial Dilated Attention Convolutional Transformer(GDacFormer). GDacFormer enhances interactions between tumor regions while balancing global and local information through the integration of adversarial learning with an improved transformer module. Specifically, GDacFormer leverages a generative adversarial segmentation network to learn richer and more detailed features. It integrates a novel Transformer module, DacFormer, featuring multi-scale dilated attention and a next convolution block. This module, embedded within the generator, aggregates semantic multi-scale information, efficiently reduces the redundancy in the self-attention mechanism, and enhances local feature representations, thus refining the brain tumor segmentation results. GDacFormer achieves Dice values for whole tumor, core tumor, and enhancing tumor segmentation of 90.9%/90.8%/93.7%, 84.6%/85.7%/93.5%, and 77.9%/79.3%/86.3% on BraTS2019-2021 datasets. Extensive evaluations demonstrate the effectiveness and competitiveness of GDacFormer. The code for GDacFormer will be made publicly available at https://github.com/MuqinZ/GDacFormer.

Autism spectrum disorder (ASD) is a multifaceted neurodevelopmental disorder featuring impaired social interactions and communication abilities engaging the individuals in a restrictive or repetitive behaviour. Though incurable early detection and intervention can reduce the severity of symptoms. Structural magnetic resonance imaging (sMRI) can improve diagnostic accuracy, facilitating early diagnosis to offer more tailored care. With the emergence of deep learning (DL), neuroimaging-based approaches for ASD diagnosis have been focused. However, many existing models lack interpretability of their decisions for diagnosis. The prime objective of this work is to perform ASD classification precisely and to interpret the classification process in a better way so as to discern the major features that are appropriate for the prediction of disorder. The proposed model employs neural architecture search network - mobile(NASNet-Mobile) model for ASD detection, which is integrated with an explainable artificial intelligence (XAI) technique called local interpretable model-agnostic explanations (LIME) for increased transparency of ASD classification. The model is trained on sMRI images of two age groups taken from autism brain imaging data exchange-I (ABIDE-I) dataset. The proposed model yielded accuracy of 0.9607, F1-score of 0.9614, specificity of 0.9774, sensitivity of 0.9451, negative predicted value (NPV) of 0.9429, positive predicted value (PPV) of 0.9783 and the diagnostic odds ratio of 745.59 for 2 to 11 years age group compared to 12 to 18 years group. These results are superior compared to other state of the art models Inception v3 and SqueezeNet.

In mechanical thrombectomy (MT), extracranial vascular tortuosity is among the main determinants of procedure duration and success. Currently, no rapid and reliable method exists to identify the anatomical features precluding fast and stable access to the cervical vessels. A retrospective sample of 513 patients were included in this study. Patients underwent first-line transfemoral MT following anterior circulation large vessel occlusion stroke. Difficult transfemoral access (DTFA) was defined as impossible common carotid catheterization or time from groin puncture to first carotid angiogram >30 min. A machine learning model based on 29 anatomical features automatically extracted from head-and-neck computed tomography angiography (CTA) was developed to predict DTFA. Three experienced raters independently assessed the likelihood of DTFA on a reduced cohort of 116 cases using a Likert scale as benchmark for the model, using preprocedural CTA as well as automatic 3D vascular segmentation separately. Among the study population, 11.5% of procedures (59/513) presented DTFA. Six different features from the aortic, supra-aortic, and cervical regions were included in the model. Cross-validation resulted in an area under the receiver operating characteristic (AUROC) curve of 0.76 (95% CI 0.75 to 0.76) for DTFA prediction, with high sensitivity for impossible access identification (0.90, 95% CI 0.81 to 0.94). The model outperformed human assessment in the reduced cohort [F1-score (95% CI) by experts with CTA: 0.43 (0.37 to 0.50); experts with 3D segmentation: 0.50 (0.46 to 0.54); and model: 0.70 (0.65 to 0.75)]. A fully automatic model for DTFA prediction was developed and validated. The presented method improved expert assessment of difficult access prediction in stroke MT. Derived information could be used to guide decisions regarding arterial access for MT.

CT angiography (CTA) is a commonly used clinical examination to detect abnormal arteries and diagnose pulmonary sequestration (PS). Reducing the radiation dose, contrast medium dosage, and injection pressure in CTA, especially in children, has always been an important research topic, but few research is proven by pathology. The current study aimed to evaluate the diagnostic accuracy for children with PS in a quadruple-low CTA (4L-CTA: low tube voltage, radiation, contrast medium, and injection flow rate) using deep learning image reconstruction (DLIR) in comparison with routine protocol CTA with adaptive statistical iterative reconstruction-V (ASIR-V) MATERIALS AND METHODS: 53 patients (1.50±1.36years) suspected with PS were enrolled to undergo chest 4L-CTA using 70kVp tube voltage with radiation dose or 0.90 mGy in volumetric CT dose index (CTDIvol) and contrast medium dose of 0.8 ml/kg injected in 16 s. Images were reconstructed using DLIR. Another 53 patients (1.25±1.02years) with a routine dose protocol was used for comparison, and images were reconstructed with ASIR-V. The contrast-to-noise ratio (CNR) and edge-rise distance (ERD) of the aorta were calculated. The subjective overall image quality and artery visualization were evaluated using a 5-point scale (5, excellent; 3, acceptable). All patients underwent surgery after CT, the sensitivity and specificity for diagnosing PS were calculated. 4L-CTA reduced radiation dose by 51%, contrast dose by 47%, injection flow rate by 44% and injection pressure by 44% compared to the routine CTA (all p<0.05). Both groups had satisfactory subjective image quality and achieved 100% in both sensitivity and specificity for diagnosing PS. 4L-CTA had a reduced CNR (by 27%, p<0.05) but similar ERD, which reflects the image spatial resolution (p>0.05) compared to the routine CTA. 4L-CTA revealed small arteries with a diameter of 0.8 mm. DLIR ensures the realization of 4L-CTA in children with PS for significant radiation and contrast dose reduction, while maintaining image quality, visualization of small arteries, and high diagnostic accuracy.

The aim of this study is to develop a deep learning-based multimodal feature interaction-guided fusion (DL-MFIF) framework that integrates macroscopic information from computed tomography (CT) images with microscopic information from whole-slide images (WSIs) to predict the epidermal growth factor receptor (EGFR) mutations of primary lung adenocarcinoma in patients with advanced-stage disease. Data from 396 patients with lung adenocarcinoma across two medical institutions were analyzed. The data from 243 cases were divided into a training set (n=145) and an internal validation set (n=98) in a 6:4 ratio, and data from an additional 153 cases from another medical institution were included as an external validation set. All cases included CT scan images and WSIs. To integrate multimodal information, we developed the DL-MFIF framework, which leverages deep learning techniques to capture the interactions between radiomic macrofeatures derived from CT images and microfeatures obtained from WSIs. Compared to other classification models, the DL-MFIF model achieved significantly higher area under the curve (AUC) values. Specifically, the model outperformed others on both the internal validation set (AUC=0.856, accuracy=0.750) and the external validation set (AUC=0.817, accuracy=0.708). Decision curve analysis (DCA) demonstrated that the model provided superior net benefits(range 0.15-0.87). Delong's test for external validation confirmed the statistical significance of the results (P<0.05). The DL-MFIF model demonstrated excellent performance in evaluating and distinguishing the EGFR in patients with advanced lung adenocarcinoma. This model effectively aids radiologists in accurately classifying EGFR mutations in patients with primary lung adenocarcinoma, thereby improving treatment outcomes for this population.

CT imaging provides essential information about internal anatomy; however, conventional CT imaging delivers radiation doses that can become problematic for patients requiring repeated imaging, highlighting the need for dose-reduction techniques. This study aims to reduce radiation doses without compromising image quality. We propose an approach that combines Neural Attenuation Fields (NAF) with an active learning strategy to better optimize CT reconstructions given a limited number of X-ray projections. Our method uses a secondary neural network to predict the Peak Signal-to-Noise Ratio (PSNR) of 2D projections generated by NAF from a range of angles in the operational range of the CT scanner. This prediction serves as a guide for the active learning process in choosing the most informative projections. In contrast to conventional techniques that acquire all X-ray projections in a single session, our technique iteratively acquires projections. The iterative process improves reconstruction quality, reduces the number of required projections, and decreases patient radiation exposure. We tested our methodology on spinal imaging using a limited subset of the VerSe 2020 dataset. We compare image quality metrics (PSNR3D, SSIM3D, and PSNR2D) to the baseline method and find significant improvements. Our method achieves the same quality with 36 projections as the baseline method achieves with 60. Our findings demonstrate that our approach achieves high-quality 3D CT reconstructions from sparse data, producing clearer and more detailed images of anatomical structures. This work lays the groundwork for advanced imaging techniques, paving the way for safer and more efficient medical imaging procedures.

High-resolution magnetic resonance angiography (~ 50 μm³ MRA) data plays a critical role in the accurate diagnosis of various vascular disorders. However, it is very challenging to acquire, and it is susceptible to artifacts and noise which limits its ability to visualize smaller blood vessels and necessitates substantial noise reduction measures. Among many techniques, the BM4D filter is a state-of-the-art denoising technique but comes with high computational cost, particularly for high-resolution 3D MRA data. In this research, five different optimized convolutional neural networks were utilized to denoise contrast-enhanced UTE-MRA data using a supervised learning approach. Since noise-free MRA data is challenging to acquire, the denoised image using BM4D filter was used as ground truth and this research mainly focused on reducing computational cost and inference time for denoising high-resolution UTE-MRA data. All five models were able to generate nearly similar denoised data compared to the ground truth with different computational footprints. Among all, the nested-UNet model generated almost similar images with the ground truth and achieved SSIM, PSNR, and MSE of 0.998, 46.12, and 3.38e-5 with 3× faster inference time than the BM4D filter. In addition, most optimized models like UNet and attention-UNet models generated nearly similar images with nested-UNet but 8.8× and 7.1× faster than the BM4D filter. In conclusion, using highly optimized networks, we have shown the possibility of denoising high-resolution UTE-MRA data with significantly shorter inference time, even with limited datasets from animal models. This can potentially make high-resolution 3D UTE-MRA data to be less computationally burdensome.

Synthetic CT (sCT) generation from cone-beam CT (CBCT) must maintain stable performance and allow for accurate dose calculation across all treatment fractions to effectively support adaptive proton therapy. This study evaluated a 3D deep-learning (DL) network for sCT generation for prostate cancer patients over the full treatment course. Patient data from 25/6 prostate cancer patients were used to train/test the DL network. Patients in the test set had a planning CT, 39 CBCT images, and at least one repeat CT (reCT) used for replanning. The generated sCT images were compared to fan-beam planning and reCT images in terms of i) CT number accuracy and stability within spherical regions-of-interest (ROIs) in the bladder, prostate, and femoral heads, ii) proton range calculation accuracy through single-spot plans, and iii) dose trends in target coverage over the treatment course (one patient). The sCT images demonstrated image quality comparable to CT, while preserving the CBCT anatomy. The mean CT numbers on the sCT and CT images were comparable, e.g. for the prostate ROI they ranged from 29 HU to 59 HU for sCT, and from 36 HU to 50 HU for CT. The largest median proton range difference was 1.9 mm. Proton dose calculations showed excellent target coverage (V95%≥99.6 %) for the high-dose target. The DL network effectively generated high-quality sCT images with CT numbers, proton range, and dose characteristics comparable to fan-beam CT. Its robustness against intra-patient variations makes it a feasible tool for adaptive proton therapy.