TY - JOUR
T1 - Development of Robust CNN Architecture for Grading and Classification of Renal Cell Carcinoma Histology Images
AU - Chanchal, Amit Kumar
AU - Lal, Shyam
AU - Suresh, Shilpa
N1 - Publisher Copyright:
© 2013 IEEE.
PY - 2025
Y1 - 2025
N2 - Kidney cancer is a commonly diagnosed cancer disease in recent years, and Renal Cell Carcinoma (RCC) is the most common kidney cancer responsible for 80% to 85% of all renal tumors. The diagnosis of kidney cancer requires manual examination and analysis of histopathological images of the affected tissue. This process is time-consuming, prone to human error, and highly depends on the expertise of a pathologist. Early detection and grading of kidney cancer tissues enable doctors and practitioners to decide the further course of treatment. Therefore, quick and precise analysis of kidney cancer tissue images is extremely important for proper diagnosis. Recently, deep learning algorithms have proved to be very efficient and accurate in histopathology image analysis. In this paper, we propose a computationally efficient deep-learning architecture based on convolutional neural networks (CNNs) to automate the grading and classification task for kidney cancer tissue. The proposed Robust CNN (RoCNN) architecture is capable of learning features at varying convolutional filter sizes because of the inception modules employed in it. Squeeze and Extract (SE) blocks are used to remove unnecessary contributions from noisy channels and improve model accuracy. Concatenating samples from three different parts of architecture allows for the encompassing of varied features, further improving grading and classification accuracy. To demonstrate that the proposed model is generalized and independent of the dataset, it has experimented on two well-known datasets, the KMC kidney dataset of five different grades and the TCGA dataset of four classes. Compared to the best-performing state-of-the-art model the accuracy of RoCNN shows a significant improvement of about 4.22% and 3.01% for both datasets respectively.
AB - Kidney cancer is a commonly diagnosed cancer disease in recent years, and Renal Cell Carcinoma (RCC) is the most common kidney cancer responsible for 80% to 85% of all renal tumors. The diagnosis of kidney cancer requires manual examination and analysis of histopathological images of the affected tissue. This process is time-consuming, prone to human error, and highly depends on the expertise of a pathologist. Early detection and grading of kidney cancer tissues enable doctors and practitioners to decide the further course of treatment. Therefore, quick and precise analysis of kidney cancer tissue images is extremely important for proper diagnosis. Recently, deep learning algorithms have proved to be very efficient and accurate in histopathology image analysis. In this paper, we propose a computationally efficient deep-learning architecture based on convolutional neural networks (CNNs) to automate the grading and classification task for kidney cancer tissue. The proposed Robust CNN (RoCNN) architecture is capable of learning features at varying convolutional filter sizes because of the inception modules employed in it. Squeeze and Extract (SE) blocks are used to remove unnecessary contributions from noisy channels and improve model accuracy. Concatenating samples from three different parts of architecture allows for the encompassing of varied features, further improving grading and classification accuracy. To demonstrate that the proposed model is generalized and independent of the dataset, it has experimented on two well-known datasets, the KMC kidney dataset of five different grades and the TCGA dataset of four classes. Compared to the best-performing state-of-the-art model the accuracy of RoCNN shows a significant improvement of about 4.22% and 3.01% for both datasets respectively.
UR - https://www.scopus.com/pages/publications/105010181131
UR - https://www.scopus.com/pages/publications/105010181131#tab=citedBy
U2 - 10.1109/ACCESS.2025.3586935
DO - 10.1109/ACCESS.2025.3586935
M3 - Article
AN - SCOPUS:105010181131
SN - 2169-3536
VL - 13
SP - 121849
EP - 121867
JO - IEEE Access
JF - IEEE Access
ER -