In surgical oncology, it is challenging for surgeons to identify lymph nodes and completely resect cancer even with pre-operative imaging systems like PET and CT, because of the lack of reliable intraoperative visualization tools. Endoscopic radio-guided cancer detection and resection has recently been evaluated whereby a novel tethered laparoscopic gamma detector is used to localize a preoperatively injected radiotracer. This can both enhance the endoscopic imaging and complement preoperative nuclear imaging data. However, gamma activity visualization is challenging to present to the operator because the probe is non-imaging and it does not visibly indicate the activity origination on the tissue surface. Initial failed attempts used segmentation or geometric methods, but led to the discovery that it could be resolved by leveraging high-dimensional image features and probe position information. To demonstrate the effectiveness of this solution, we designed and implemented a simple regression network that successfully addressed the problem. To further validate the proposed solution, we acquired and publicly released two datasets captured using a custom-designed, portable stereo laparoscope system. Through intensive experimentation, we demonstrated that our method can successfully and effectively detect the sensing area, establishing a new performance benchmark. Code and data are available at https://github.com/br0202/Sensing_area_detection.git
Given the close association between colorectal cancer and polyps, the diagnosis and identification of colorectal polyps play a critical role in the detection and surgical intervention of colorectal cancer. In this context, the automatic detection and segmentation of polyps from various colonoscopy images has emerged as a significant problem that has attracted broad attention. Current polyp segmentation techniques face several challenges: firstly, polyps vary in size, texture, color, and pattern; secondly, the boundaries between polyps and mucosa are usually blurred, existing studies have focused on learning the local features of polyps while ignoring the long-range dependencies of the features, and also ignoring the local context and global contextual information of the combined features. To address these challenges, we propose FLDNet (Foreground-Long-Distance Network), a Transformer-based neural network that captures long-distance dependencies for accurate polyp segmentation. Specifically, the proposed model consists of three main modules: a pyramid-based Transformer encoder, a local context module, and a foreground-Aware module. Multilevel features with long-distance dependency information are first captured by the pyramid-based transformer encoder. On the high-level features, the local context module obtains the local characteristics related to the polyps by constructing different local context information. The coarse map obtained by decoding the reconstructed highest-level features guides the feature fusion process in the foreground-Aware module of the high-level features to achieve foreground enhancement of the polyps. Our proposed method, FLDNet, was evaluated using seven metrics on common datasets and demonstrated superiority over state-of-the-art methods on widely-used evaluation measures.
Gastric cancer is the third leading cause of cancer-related mortality worldwide, but no guideline-recommended screening test exists. Existing methods can be invasive, expensive, and lack sensitivity to identify early-stage gastric cancer. In this study, we explore the feasibility of using a deep learning approach on non-contrast CT scans for gastric cancer detection. We propose a novel cluster-induced Mask Transformer that jointly segments the tumor and classifies abnormality in a multi-task manner. Our model incorporates learnable clusters that encode the texture and shape prototypes of gastric cancer, utilizing self- and cross-attention to interact with convolutional features. In our experiments, the proposed method achieves a sensitivity of 85.0% and specificity of 92.6% for detecting gastric tumors on a hold-out test set consisting of 100 patients with cancer and 148 normal. In comparison, two radiologists have an average sensitivity of 73.5% and specificity of 84.3%. We also obtain a specificity of 97.7% on an external test set with 903 normal cases. Our approach performs comparably to established state-of-the-art gastric cancer screening tools like blood testing and endoscopy, while also being more sensitive in detecting early-stage cancer. This demonstrates the potential of our approach as a novel, non-invasive, low-cost, and accurate method for opportunistic gastric cancer screening.
Machine learning (ML) is a branch of Artificial Intelligence (AI) where computers analyze data and find patterns in the data. The study focuses on the detection of metastatic cancer using ML. Metastatic cancer is the point where the cancer has spread to other parts of the body and is the cause of approximately 90% of cancer related deaths. Normally, pathologists spend hours each day to manually classify whether tumors are benign or malignant. This tedious task contributes to mislabeling metastasis being over 60% of time and emphasizes the importance to be aware of human error, and other inefficiencies. ML is a good candidate to improve the correct identification of metastatic cancer saving thousands of lives and can also improve the speed and efficiency of the process thereby taking less resources and time. So far, deep learning methodology of AI has been used in the research to detect cancer. This study is a novel approach to determine the potential of using preprocessing algorithms combined with classification algorithms in detecting metastatic cancer. The study used two preprocessing algorithms: principal component analysis (PCA) and the genetic algorithm to reduce the dimensionality of the dataset, and then used three classification algorithms: logistic regression, decision tree classifier, and k-nearest neighbors to detect metastatic cancer in the pathology scans. The highest accuracy of 71.14% was produced by the ML pipeline comprising of PCA, the genetic algorithm, and the k-nearest neighbors algorithm, suggesting that preprocessing and classification algorithms have great potential for detecting metastatic cancer.
Early detection and localization of pancreatic cancer can increase the 5-year survival rate for patients from 8.5% to 20%. Artificial intelligence (AI) can potentially assist radiologists in detecting pancreatic tumors at an early stage. Training AI models require a vast number of annotated examples, but the availability of CT scans obtaining early-stage tumors is constrained. This is because early-stage tumors may not cause any symptoms, which can delay detection, and the tumors are relatively small and may be almost invisible to human eyes on CT scans. To address this issue, we develop a tumor synthesis method that can synthesize enormous examples of small pancreatic tumors in the healthy pancreas without the need for manual annotation. Our experiments demonstrate that the overall detection rate of pancreatic tumors, measured by Sensitivity and Specificity, achieved by AI trained on synthetic tumors is comparable to that of real tumors. More importantly, our method shows a much higher detection rate for small tumors. We further investigate the per-voxel segmentation performance of pancreatic tumors if AI is trained on a combination of CT scans with synthetic tumors and CT scans with annotated large tumors at an advanced stage. Finally, we show that synthetic tumors improve AI generalizability in tumor detection and localization when processing CT scans from different hospitals. Overall, our proposed tumor synthesis method has immense potential to improve the early detection of pancreatic cancer, leading to better patient outcomes.
Computer aided detection and diagnosis systems based on deep learning have shown promising performance in breast cancer detection. However, there are cases where the obtained results lack justification. In this study, our objective is to highlight the regions of interest used by a convolutional neural network (CNN) for classifying histological images as benign or malignant. We compare these regions with the regions identified by pathologists. To achieve this, we employed the VGG19 architecture and tested three visualization methods: Gradient, LRP Z, and LRP Epsilon. Additionally, we experimented with three pixel selection methods: Bins, K-means, and MeanShift. Based on the results obtained, the Gradient visualization method and the MeanShift selection method yielded satisfactory outcomes for visualizing the images.
Magnetic resonance imaging (MRI) is the most sensitive technique for breast cancer detection among current clinical imaging modalities. Contrast-enhanced MRI (CE-MRI) provides superior differentiation between tumors and invaded healthy tissue, and has become an indispensable technique in the detection and evaluation of cancer. However, the use of gadolinium-based contrast agents (GBCA) to obtain CE-MRI may be associated with nephrogenic systemic fibrosis and may lead to bioaccumulation in the brain, posing a potential risk to human health. Moreover, and likely more important, the use of gadolinium-based contrast agents requires the cannulation of a vein, and the injection of the contrast media which is cumbersome and places a burden on the patient. To reduce the use of contrast agents, diffusion-weighted imaging (DWI) is emerging as a key imaging technique, although currently usually complementing breast CE-MRI. In this study, we develop a multi-sequence fusion network to synthesize CE-MRI based on T1-weighted MRI and DWIs. DWIs with different b-values are fused to efficiently utilize the difference features of DWIs. Rather than proposing a pure data-driven approach, we invent a multi-sequence attention module to obtain refined feature maps, and leverage hierarchical representation information fused at different scales while utilizing the contributions from different sequences from a model-driven approach by introducing the weighted difference module. The results show that the multi-b-value DWI-based fusion model can potentially be used to synthesize CE-MRI, thus theoretically reducing or avoiding the use of GBCA, thereby minimizing the burden to patients. Our code is available at \url{https://github.com/Netherlands-Cancer-Institute/CE-MRI}.
Breast cancer is the second most responsible for all cancer types and has been the cause of numerous deaths over the years, especially among women. Any improvisation of the existing diagnosis system for the detection of cancer can contribute to minimizing the death ratio. Moreover, cancer detection at an early stage has recently been a prime research area in the scientific community to enhance the survival rate. Proper choice of machine learning tools can ensure early-stage prognosis with high accuracy. In this paper, we have studied different machine learning algorithms to detect whether a patient is likely to face breast cancer or not. Due to the implicit behavior of early-stage features, we have implemented a multilayer perception model with the integration of PCA and suggested it to be more viable than other detection algorithms. Our 4 layers MLP-PCA network has obtained the best accuracy of 100% with a mean of 90.48% accuracy on the BCCD dataset.
Early detection of cancers has been much explored due to its paramount importance in biomedical fields. Among different types of data used to answer this biological question, studies based on T cell receptors (TCRs) are under recent spotlight due to the growing appreciation of the roles of the host immunity system in tumor biology. However, the one-to-many correspondence between a patient and multiple TCR sequences hinders researchers from simply adopting classical statistical/machine learning methods. There were recent attempts to model this type of data in the context of multiple instance learning (MIL). Despite the novel application of MIL to cancer detection using TCR sequences and the demonstrated adequate performance in several tumor types, there is still room for improvement, especially for certain cancer types. Furthermore, explainable neural network models are not fully investigated for this application. In this article, we propose multiple instance neural networks based on sparse attention (MINN-SA) to enhance the performance in cancer detection and explainability. The sparse attention structure drops out uninformative instances in each bag, achieving both interpretability and better predictive performance in combination with the skip connection. Our experiments show that MINN-SA yields the highest area under the ROC curve (AUC) scores on average measured across 10 different types of cancers, compared to existing MIL approaches. Moreover, we observe from the estimated attentions that MINN-SA can identify the TCRs that are specific for tumor antigens in the same T cell repertoire.
Computational pathology methods have the potential to improve access to precision medicine, as well as the reproducibility and accuracy of pathological diagnoses. Particularly the analysis of whole-slide-images (WSIs) of immunohistochemically (IHC) stained tissue sections could benefit from computational pathology methods. However, scoring biomarkers such as KI67 in IHC WSIs often necessitates the detection of areas of invasive cancer. Training cancer detection models often requires annotations, which is time-consuming and therefore costly. Currently, cancer regions are typically annotated in WSIs of haematoxylin and eosin (H&E) stained tissue sections. In this study, we investigate the possibility to register annotations that were made in H&E WSIs to their IHC counterparts. Two pathologists annotated regions of invasive cancer in WSIs of 272 breast cancer cases. For each case, a matched H&E and KI67 WSI are available, resulting in 544 WSIs with invasive cancer annotations. We find that cancer detection CNNs that were trained with annotations registered from the H&E to the KI67 WSIs only differ slightly in calibration but not in performance compared to cancer detection models trained on annotations made directly in the KI67 WSIs in a test set consisting of 54 cases. The mean slide-level AUROC is 0.974 [0.964, 0.982] for models trained with the KI67 annotations and 0.974 [0.965, 0.982] for models trained using registered annotations. This indicates that WSI registration has the potential to reduce the need for IHC-specific annotations. This could significantly increase the usefulness of already existing annotations.