Classification of cancer cellularity within tissue samples is currently a manual process performed by pathologists. This process of correctly determining cancer cellularity can be time intensive. Deep Learning (DL) techniques in particular have become increasingly more popular for this purpose, due to the accuracy and performance they exhibit, which can be comparable to the pathologists. This work investigates the capabilities of two DL approaches to assess cancer cellularity in whole slide images (WSI) in the SPIE-AAPM-NCI BreastPathQ challenge dataset. The effects of training on augmented data via rotations, and combinations of multiple architectures into a single network were analyzed using a modified Kendall Tau-b prediction probability metric known as the average prediction probability PK. A deep, transfer learned, Convolutional Neural Network (CNN) InceptionV3 was used as a baseline, achieving an average PK value of 0.884, showing improvement from the average PK value of 0.83 achieved by pathologists. The network was then trained on additional training datasets which were rotated between 1 and 360 degrees, which saw a peak increase of PK up to 4.2%. An additional architecture consisting of the InceptionV3 network and VGG16, a shallow, transfer learned CNN, was combined in a parallel architecture. This parallel architecture achieved a baseline average PK value of 0.907, a statistically significantly improvement over either of the architectures' performances separately (p<0.0001 by unpaired t-test).
翻译:组织样本中的癌症细胞分类目前是一个由病理学家执行的人工过程。 正确确定癌症细胞性的过程可以时间密集。 深学习(DL)技术由于准确性和性能,可以与病理学家相仿,因此在这方面越来越受欢迎。 这项工作调查了两种DL方法在SPIE-APM-NCI CampalPathQ挑战数据集中用整张幻灯片图像评估癌症细胞性的能力(WSI),与SPIE-AMM-NCI-NCI Campal PathQ挑战数据集中平均0.83PK值相比,平均PK值的平均值提高了。 培训对通过轮换增加数据以及将多个结构合并成一个单一网络的影响进行了分析,使用一个修改后的Kendall Tau-b预测概率指标,称为平均预测概率PK。 深、学过、学过、进过、进进进进的进进进神经系统网络(CNISMIS)3的平行结构得到了显著的升级。 一级结构由SISNISV的平行结构得到了显著的升级。