Three-Dimensional Printed Molds for Image-Guided Surgical Biopsies: An Open Source Computational Platform

Author:

Crispin-Ortuzar Mireia1,Gehrung Marcel1,Ursprung Stephan12,Gill Andrew B.2,Warren Anne Y.3,Beer Lucian24,Gallagher Ferdia A.2,Mitchell Thomas J.56,Mendichovszky Iosif A.27,Priest Andrew N.27,Stewart Grant D.5,Sala Evis12,Markowetz Florian1

Affiliation:

1. Cancer Research UK, Cambridge Institute, University of Cambridge, Cambridge, United Kingdom

2. Department of Radiology, University of Cambridge, Cambridge, United Kingdom

3. Department of Histopathology, Cambridge University Hospitals National Health Service (NHS) Foundation Trust, Cambridge, United Kingdom

4. Department of Biomedical Imaging and Image-Guided Therapy, Medical University Vienna, Vienna, Austria

5. Department of Surgery, University of Cambridge, Cambridge, United Kingdom

6. Wellcome Trust Sanger Institute, Hinxton, United Kingdom

7. Department of Radiology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom

Abstract

PURPOSE Spatial heterogeneity of tumors is a major challenge in precision oncology. The relationship between molecular and imaging heterogeneity is still poorly understood because it relies on the accurate coregistration of medical images and tissue biopsies. Tumor molds can guide the localization of biopsies, but their creation is time consuming, technologically challenging, and difficult to interface with routine clinical practice. These hurdles have so far hindered the progress in the area of multiscale integration of tumor heterogeneity data. METHODS We have developed an open-source computational framework to automatically produce patient-specific 3-dimensional–printed molds that can be used in the clinical setting. Our approach achieves accurate coregistration of sampling location between tissue and imaging, and integrates seamlessly with clinical, imaging, and pathology workflows. RESULTS We applied our framework to patients with renal cancer undergoing radical nephrectomy. We created personalized molds for 6 patients, obtaining Dice similarity coefficients between imaging and tissue sections ranging from 0.86 to 0.96 for tumor regions and between 0.70 and 0.76 for healthy kidneys. The framework required minimal manual intervention, producing the final mold design in just minutes, while automatically taking into account clinical considerations such as a preference for specific cutting planes. CONCLUSION Our work provides a robust and automated interface between imaging and tissue samples, enabling the development of clinical studies to probe tumor heterogeneity on multiple spatial scales.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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