# LUMBER: A feasible MRI‐based 3D printed mould platform for ex vivo sampling of prostate cancer

**Authors:** Chris Du, Goran Rac, Nicholas Lanzotti, Jeffrey Ellis, Victor Chen, Maria M. Picken, Guliz A. Barkan, Michael Woods, Alex Gorbonos, Marcus Quek, Steven M. Shea, Gopal N. Gupta

PMC · DOI: 10.1002/bco2.70161 · BJUI Compass · 2026-02-24

## TL;DR

A new 3D-printed mold platform was developed to collect fresh prostate cancer tissue during surgery, enabling future cancer research.

## Contribution

A novel MRI-based 3D-printed mold platform for ex vivo sampling of prostate cancer tissue during radical prostatectomy.

## Key findings

- Ex vivo biopsies using the 3D-printed mold successfully yielded prostate cancer tissue in all 12 patients.
- The platform allows reliable sampling of MRI-identified and biopsy-proven prostate cancer lesions.
- The method could advance research by providing viable cancer tissue for further study.

## Abstract

Accurate, reliable means to obtain fresh viable clinically localised prostate cancer tissue do not exist. We developed a method in which bespoke 3D‐printed moulds can be created for any prostate and allow for ex vivo sampling of magnetic resonance imaging (MRI)‐visible, biopsy‐proven cancer lesions. We sought to demonstrate the ability of our platform to obtain fresh viable prostate cancer tissue after robot‐assisted radical prostatectomy (RARP).

Inclusion criteria were a patient that underwent MR‐fusion biopsy (UroNav, Philips) with a resulting biopsy proven Gleason Grade (GG) ≥ 2 target. STL files for prostate boundary and target regions of interest (ROI), created as part of fusion biopsy, were exported from the UroNav and imported into SolidWorks (Dassault), a solid modelling computer‐aided design and engineering application. A macro within SolidWorks was then applied to create a material‐optimised mould around the prostate with needle guides to allow for targeted sampling. The 3D mould was exported as an STL file and then 3D‐printed on a Stratasys Fortus 250 MC 3D Printer. During RARP, the specimen is extracted, the seminal vesicles detached and the prostate is placed in the mould for biopsy. The biopsy cores are sent to pathology for analysis and compared to specimens from the initial biopsy.

Twelve patients with MRI‐visible lesions and biopsy proven GGG ≥ 2 cancer underwent RARP. In 12 out of 12 patients, ex vivo biopsies performed with the 3D‐printed mould yielded prostate tissue with cancer.

Our 3D‐printed mould platform allows for ex vivo sampling of MRI identified and previously biopsied prostate cancer at the time of RARP. The native, cancerous tissue may then be used to advance further research. The potential applications for a platform that can reliably sample living prostate cancer tissue are numerous, including the ability to advance future cancer research as well as other solid‐organ malignancies with targetable lesions.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}
- **Diseases:** prostate (MESH:D011472), -organ malignancies (MESH:D009369), prostate cancer (MESH:D011471)
- **Chemicals:** formalin (MESH:D005557), eosin (MESH:D004801), haematoxylin (MESH:D006416), RARP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932066/full.md

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Source: https://tomesphere.com/paper/PMC12932066