Improving the Generalizability of Deep Learning for T2-Lesion Segmentation of Gliomas in the Post-Treatment Setting

Author:

Ellison Jacob123ORCID,Caliva Francesco12ORCID,Damasceno Pablo12ORCID,Luks Tracy L.1,LaFontaine Marisa1ORCID,Cluceru Julia12,Kemisetti Anil1,Li Yan12ORCID,Molinaro Annette M.4,Pedoia Valentina123,Villanueva-Meyer Javier E.12,Lupo Janine M.123ORCID

Affiliation:

1. Department of Radiology and Biomedical Imaging, UCSF, San Francisco, CA 94143, USA

2. Center for Intelligent Imaging, UCSF, San Francisco, CA 94143, USA

3. UCSF/UC Berkeley Graduate Program in Bioengineering, San Francisco, CA 94143, USA

4. Department of Neurological Surgery, UCSF, San Francisco, CA 94143, USA

Abstract

Although fully automated volumetric approaches for monitoring brain tumor response have many advantages, most available deep learning models are optimized for highly curated, multi-contrast MRI from newly diagnosed gliomas, which are not representative of post-treatment cases in the clinic. Improving segmentation for treated patients is critical to accurately tracking changes in response to therapy. We investigated mixing data from newly diagnosed (n = 208) and treated (n = 221) gliomas in training, applying transfer learning (TL) from pre- to post-treatment imaging domains, and incorporating spatial regularization for T2-lesion segmentation using only T2 FLAIR images as input to improve generalization post-treatment. These approaches were evaluated on 24 patients suspected of progression who had received prior treatment. Including 26% of treated patients in training improved performance by 13.9%, and including more treated and untreated patients resulted in minimal changes. Fine-tuning with treated glioma improved sensitivity compared to data mixing by 2.5% (p < 0.05), and spatial regularization further improved performance when used with TL by 95th HD, Dice, and sensitivity (6.8%, 0.8%, 2.2%; p < 0.05). While training with ≥60 treated patients yielded the majority of performance gain, TL and spatial regularization further improved T2-lesion segmentation to treated gliomas using a single MR contrast and minimal processing, demonstrating clinical utility in response assessment.

Funder

National Institutes of Health

Department of Defense

UCSF Helen Diller Family Cancer Center Cancer Imaging Resources Pilot Grant

Publisher

MDPI AG

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