The morphological features that pathologists use to differentiate neoplasms from normal tissue are nonspecific to tissue type. For example, if given a Ki67 stained biopsy of neuroendocrine or breast tumor, a pathologist would be able to correctly identify morphologically abnormal cells in both samples but may struggle to identify the origin of both samples. This is also true for other pathological malignancies such as carcinomas, sarcomas, and leukemia. This implies that computer algorithms trained to recognize tumor from one site should be able to identify tumor from other sites with similar tumor subtypes. Here, we present the results of an experiment that supports this hypothesis. We train a deep learning system to distinguish tumor from non-tumor regions in Ki67 stained neuroendocrine tumor digital slides. Then, we test the same, unmodified, deep learning model to distinguish breast cancer from non-cancer regions. When applied to a sample of 96 high power fields, our system achieved a cumulative pixel-wise accuracy of 86% across these high-power fields. To our knowledge, our results are the first to formally demonstrate generalized segmentation of tumors from different sites of origin through image analysis. This paradigm has the potential to help with the design of tumor identification algorithms as well as the composition of the datasets they draw from.
Follicular Lymphoma (FL) is the second most common subtype of lymphoma in the Western World. It is a low-grade lymphoma arising from Germinal Centre (GC) B cells. The neoplasm predominantly consists of back-to-back arrangement of nodules or follicles of transformed GC B cells with the replacement of lymph node architecture and loss of normal cortex and medullary differentiation, which is preserved in non-neoplastic or reactive lymph node. There is a growing interest in studying different cell subsets inside and on the periphery of the follicles to direct curative therapies and minimize treatment-related complications. To facilitate this analysis, we develop an automated method for follicle detection from images of CD8 stained histopathological slides. The proposed method is trained on eight whole digital slides. The method is inspired by U-net to segment follicles from the whole slide images. The results on an independent dataset resulted in an average Dice similarity coefficient of 85.6% when compared to an expert pathologist’s annotations. We expect that the method will play a considerable role for comparing the ratios of different subsets of cells inside and at the periphery of the follicles.
Identification of bladder layers from tissue biopsies is the first step towards an accurate diagnosis and prognosis of bladder cancer. We present an automated Bladder Image Analysis System (BLIAS) that can recognize urothelium, lamina propria, and muscularis propria from images of H and E-stained slides of bladder biopsies. Furthermore, we present its clinical application to automate risk stratification of T1 bladder cancer patients based on the depth of lamina propria invasion. The method uses multidimensional scaling and transfer learning in conjunction with convolutional neural networks to identify different bladder layers from H and E images of bladder biopsies. The method was trained and tested on eighty whole slide images of bladder cancer biopsies. Our preliminary findings suggest that the proposed method has good agreement with the pathologist in identification of different bladder layers. Additionally, given a set of tumor nuclei within lamina propria, it has the potential to risk stratify T1 bladder cancer by computing the distance from this set to urothelium and muscularis propria. Our results suggest that a pretrained network trained via transfer learning is better in identifying bladder layers than a conventional deep learning paradigm.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.