Composite imaging method for histological image analysis

Author(s):  
Mizuho Imai ◽  
Akane Takei ◽  
Keita Miyamoto ◽  
Masanobu Takahashi ◽  
Masayuki Nakano
2021 ◽  
pp. 679-694
Author(s):  
Alessandra Pulvirenti ◽  
Rikiya Yamashita ◽  
Jayasree Chakraborty ◽  
Natally Horvat ◽  
Kenneth Seier ◽  
...  

PURPOSE The therapeutic management of pancreatic neuroendocrine tumors (PanNETs) is based on pathological tumor grade assessment. A noninvasive imaging method to grade tumors would facilitate treatment selection. This study evaluated the ability of quantitative image analysis derived from computed tomography (CT) images to predict PanNET grade. METHODS Institutional database was queried for resected PanNET (2000-2017) with a preoperative arterial phase CT scan. Radiomic features were extracted from the primary tumor on the CT scan using quantitative image analysis, and qualitative radiographic descriptors were assessed by two radiologists. Significant features were identified by univariable analysis and used to build multivariable models to predict PanNET grade. RESULTS Overall, 150 patients were included. The performance of models based on qualitative radiographic descriptors varied between the two radiologists (reader 1: sensitivity, 33%; specificity, 66%; negative predictive value [NPV], 63%; and positive predictive value [PPV], 37%; reader 2: sensitivity, 45%; specificity, 70%; NPV, 72%; and PPV, 47%). The model based on radiomics had a better performance predicting the tumor grade with a sensitivity of 54%, a specificity of 80%, an NPV of 81%, and a PPV of 54%. The inclusion of radiomics in the radiographic descriptor models improved both the radiologists' performance. CONCLUSION CT quantitative image analysis of PanNETs helps predict tumor grade from routinely acquired scans and should be investigated in future prospective studies.


2019 ◽  
Vol 116 (30) ◽  
pp. 14937-14946 ◽  
Author(s):  
Benjamin R. Kingston ◽  
Abdullah Muhammad Syed ◽  
Jessica Ngai ◽  
Shrey Sindhwani ◽  
Warren C. W. Chan

Metastasis of solid tumors is a key determinant of cancer patient survival. Targeting micrometastases using nanoparticles could offer a way to stop metastatic tumor growth before it causes excessive patient morbidity. However, nanoparticle delivery to micrometastases is difficult to investigate because micrometastases are small in size and lie deep within tissues. Here, we developed an imaging and image analysis workflow to analyze nanoparticle–cell interactions in metastatic tumors. This technique combines tissue clearing and 3D microscopy with machine learning-based image analysis to assess the physiology of micrometastases with single-cell resolution and quantify the delivery of nanoparticles within them. We show that nanoparticles access a higher proportion of cells in micrometastases (50% nanoparticle-positive cells) compared with primary tumors (17% nanoparticle-positive cells) because they reside close to blood vessels and require a small diffusion distance to reach all tumor cells. Furthermore, the high-throughput nature of our image analysis workflow allowed us to profile the physiology and nanoparticle delivery of 1,301 micrometastases. This enabled us to use machine learning-based modeling to predict nanoparticle delivery to individual micrometastases based on their physiology. Our imaging method allows researchers to measure nanoparticle delivery to micrometastases and highlights an opportunity to target micrometastases with nanoparticles. The development of models to predict nanoparticle delivery based on micrometastasis physiology could enable personalized treatments based on the specific physiology of a patient’s micrometastases.


2012 ◽  
Vol 108 (1) ◽  
pp. 388-401 ◽  
Author(s):  
G. Bueno ◽  
R. González ◽  
O. Déniz ◽  
M. García-Rojo ◽  
J. González-García ◽  
...  

2004 ◽  
Vol 207 (1) ◽  
pp. 105-110 ◽  
Author(s):  
Satomi Yokota ◽  
Akitsugu Sasaki ◽  
Yoshio Hotta ◽  
Yuji Yamane ◽  
Hideaki Kimura ◽  
...  

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