Prostate Commander is not just another generic DICOM viewer, but a lightning-fast, highly specialized analysis tool built for exactly one purpose: automatically contouring radiological cross-sectional images, presenting them to the user for review, and thereby speeding up the preparation of fusion biopsies and follow-up assessments – entirely on your own computer, with no cloud connection.
The software supports the evaluation of T2-weighted MRI scans of the prostate. It automates the most time-consuming part of preparation – tracing the organ boundaries slice by slice – and provides the result as a reviewable, correctable suggestion.
This software grew out of daily clinical practice: as a radiologist who performs MRI/ultrasound fusion prostate biopsies together with a urologist, I was confronted with a wide variety of examinations from many different sources – of correspondingly varying quality, both in the scans themselves and in the accompanying reports. To speed up the upfront validation process and quickly gain an overview of how to plan the fusion biopsy most efficiently and safely, I wrote this program.
Automated contouring of the prostate and, optionally, suspicious areas („lesions“) in axial T2 slices, as a basis for planning MRI/ultrasound fusion biopsies and for volume estimation.
Reads a DICOM series and fully automatically selects the required sequences (T2, diffusion). ADC maps are calculated independently from the diffusion images, as is the volume of the prostate and – if present – of a lesion. After AI-based contouring of the prostate, the software searches for lesions in the T2, diffusion, and ADC images – oriented on PI-RADS criteria. The complete diagnostic findings of the examination are summarized in a structured Word document.
For medical professionals in radiology and urology who assess prostate MRI series or prepare fusion biopsies and want to retain control over every automatically generated contour.
Every automatically generated contour remains a suggestion. It is color-coded as active or inactive, and can be adjusted, deleted, or redrawn slice by slice. Slices on which the AI finds no plausible segment are automatically marked inactive, rather than forcing an incorrect contour.
The application is designed as a standalone Windows program: no cloud processing, no transmission of image data to third parties. All computations run locally on the machine where it is started.
Packaged as a standalone Windows application (no separate Python installation required). Runs fully offline on standard PC hardware. An available graphics card (CUDA) is automatically used for AI computation; otherwise the application falls back to CPU-optimized processing.
A neural network specialized for medical cross-sectional images (deep-learning segmentation model) generates the suggested contour for each slice. The model can be fine-tuned as needed with additional, locally available training data.
Processes DICOM – the international standard for medical imaging data. Automatically detects the relevant axial T2 series within an examination folder and correctly assigns additional sequences (e.g. diffusion).
Image data never leaves the computer. Depending on the edition, intermediate results are either stored locally for later sessions or – in the lightweight edition – completely deleted after every session.
Programmed through direct interaction between a human and the AI coding assistant „Claude Code“ by Anthropic – making the application itself also a product of artificial intelligence. Written in Python, runs both with and without CUDA GPU support. The logic behind the lesion search was likewise developed together with Claude Code based on the PI-RADS protocol and implemented in program code.
A functionally limited, open edition is available for testing: loading exclusively via drag&drop, with no persistent data storage – all examination data is automatically and completely deleted after every session.
Contrast-enhanced sequences were deliberately omitted: abbreviated MRI protocols without contrast agent are already imminent, so the lesion search is specifically designed around T2, diffusion, and ADC.
The workflow is deliberately kept linear: load, review, correct, evaluate. Each step is individually traceable and can be interrupted at any time.
Schematic sequence showing how a substantiated lesion finding emerges from three image sequences – all illustrations are sketches, not real patient images.
Sample view of the application using entirely synthetic image data – no real patient reference. Click to enlarge.
| Key | Function |
|---|---|
| K | Start automatic AI segmentation |
| F1 | Show help |
| F2 | Generate analysis report |
| F3 | View: lesion segment |
| F5 / Esc | Cancel operation |
| P | Switch compute mode (GPU / CPU) |
Full overview of all key bindings and the operating instructions directly within the application via the Help key.
The lesion search was not handed over as a ready-made formula, but developed through dialogue: first, what radiologically defines a PI-RADS 2.1-suspicious lesion was discussed – only afterward was it worked out together with Claude Code how to translate this description into concrete, computable thresholds. Both are documented here.
The starting point was the radiological PI-RADS 2.1 description of a clinically relevant lesion, with diffusion and ADC as the leading sequences:
The key agreement: none of these features alone is sufficient – only the SIMULTANEOUS presence of all three imaging findings at the same location makes an area suspicious.
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