TY - JOUR
T1 - Improving Augmented Human Intelligence to Distinguish Burkitt Lymphoma from Diffuse Large B-Cell Lymphoma Cases
AU - Mohlman, Jeffrey S.
AU - Leventhal, Samuel D.
AU - Hansen, Taft
AU - Kohan, Jessica
AU - Pascucci, Valerio
AU - Salama, Mohamed E.
N1 - Publisher Copyright:
© American Society for Clinical Pathology, 2020. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Objectives: To assess and improve the assistive role of a deep, densely connected convolutional neural network (CNN) to hematopathologists in differentiating histologic images of Burkitt lymphoma (BL) from diffuse large B-cell lymphoma (DLBCL). Methods: A total of 10,818 images from BL (n = 34) and DLBCL (n = 36) cases were used to either train or apply different CNNs. Networks differed by number of training images and pixels of images, absence of color, pixel and staining augmentation, and depth of the network, among other parameters. Results: Cases classified correctly were 17 of 18 (94%), nine with 100% of images correct by the best performing network showing a receiver operating characteristic curve analysis area under the curve 0.92 for both DLBCL and BL. The best performing CNN used all available training images, two random subcrops per image of 448 × 448 pixels, random H&E staining image augmentation, random horizontal flipping of images, random alteration of contrast, reduction on validation error plateau of 15 epochs, block size of six, batch size of 32, and depth of 22. Other networks and decreasing training images had poorer performance. Conclusions: CNNs are promising augmented human intelligence tools for differentiating a subset of BL and DLBCL cases.
AB - Objectives: To assess and improve the assistive role of a deep, densely connected convolutional neural network (CNN) to hematopathologists in differentiating histologic images of Burkitt lymphoma (BL) from diffuse large B-cell lymphoma (DLBCL). Methods: A total of 10,818 images from BL (n = 34) and DLBCL (n = 36) cases were used to either train or apply different CNNs. Networks differed by number of training images and pixels of images, absence of color, pixel and staining augmentation, and depth of the network, among other parameters. Results: Cases classified correctly were 17 of 18 (94%), nine with 100% of images correct by the best performing network showing a receiver operating characteristic curve analysis area under the curve 0.92 for both DLBCL and BL. The best performing CNN used all available training images, two random subcrops per image of 448 × 448 pixels, random H&E staining image augmentation, random horizontal flipping of images, random alteration of contrast, reduction on validation error plateau of 15 epochs, block size of six, batch size of 32, and depth of 22. Other networks and decreasing training images had poorer performance. Conclusions: CNNs are promising augmented human intelligence tools for differentiating a subset of BL and DLBCL cases.
KW - Artificial intelligence
KW - Augmented human intelligence
KW - Augmented intelligence
KW - Burkitt lymphoma
KW - Convolutional neural network
KW - Diffuse large B-cell lymphoma
KW - Hematopathology
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U2 - 10.1093/AJCP/AQAA001
DO - 10.1093/AJCP/AQAA001
M3 - Article
C2 - 32067039
AN - SCOPUS:85085684770
SN - 0002-9173
VL - 153
SP - 743
EP - 759
JO - American Journal of Clinical Pathology
JF - American Journal of Clinical Pathology
IS - 6
ER -