Convolutional neural network with a hybrid loss function for fully automated segmentation of lymphoma lesions in FDG PET images

TL;DR

This paper introduces a fully automated CNN-based segmentation method for lymphoma lesions in FDG PET images, utilizing a hybrid loss function and multi-center data to improve accuracy and facilitate clinical quantification.

Contribution

The study develops a novel 3D U-Net model with SE modules and hybrid loss, demonstrating superior performance over standard models in multi-center lymphoma PET segmentation.

Findings

Achieved a Dice coefficient of 0.77 with the ensemble model.

Hybrid loss function outperformed other loss combinations (p<0.05).

Model enables automated quantification of tumor volume in clinical settings.

Abstract

Segmentation of lymphoma lesions is challenging due to their varied sizes and locations in whole-body PET scans. This work presents a fully-automated segmentation technique using a multi-center dataset of diffuse large B-cell lymphoma (DLBCL) with heterogeneous characteristics. We utilized a dataset of [18F]FDG-PET scans (n=194) from two different imaging centers, including cases with primary mediastinal large B-cell lymphoma (PMBCL) (n=104). Automated brain and bladder removal approaches were utilized as preprocessing steps to tackle false positives caused by normal hypermetabolic uptake in these organs. Our segmentation model is a convolutional neural network (CNN) based on a 3D U-Net architecture that includes squeeze and excitation (SE) modules. Hybrid distribution, region, and boundary-based losses (Unified Focal and Mumford-Shah (MS)) were utilized that showed the best performance compared to other combinations (p<0.05). Cross-validation between different centers, DLBCL and PMBCL cases, and three random splits were applied on train/validation data. The ensemble of these six models achieved a Dice similarity coefficient (DSC) of 0.77 +- 0.08 and Hausdorff distance (HD) of 16.5 +-12.5. Our 3D U-net model with SE modules for segmentation with hybrid loss performed significantly better (p<0.05) as compared to the 3D U-Net (without SE modules) using the same loss function (Unified Focal and MS loss) (DSC= 0.64 +-0.21 and HD= 26.3 +- 18.7). Our model can facilitate a fully automated quantification pipeline in a multi-center context that opens the possibility for routine reporting of total metabolic tumor volume (TMTV) and other metrics shown useful for the management of lymphoma.