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Bone metastases from prostate cancer: assessing treatment response by using diffusion-weighted imaging and functional
Carolin Reischauer1, Johannes M Froehlich, Dow-Mu Koh
1Institute for Biomedical Engineering, ETH and University Zurich, Zurich, Switzerland.
Diffusion-weighted MRI effectively monitors prostate cancer bone metastases during antiandrogen therapy. Increased apparent diffusion coefficient (ADC) in tumors correlated with decreased PSA levels, revealing treatment response heterogeneity.
Area of Science:
- Oncology
- Radiology
- Medical Imaging
Background:
- Prostate cancer commonly metastasizes to bone.
- Monitoring treatment response in bone metastases is crucial for patient management.
- Antiandrogen therapy is a standard treatment for advanced prostate cancer.
Purpose of the Study:
- To prospectively evaluate diffusion-weighted (DW) magnetic resonance (MR) imaging for monitoring antiandrogen therapy response in prostate cancer bone metastases.
- To assess the utility of apparent diffusion coefficient (ADC) and functional diffusion maps (DMs) in quantifying treatment effects.
Main Methods:
- Nine treatment-naive patients with prostate cancer bone metastases underwent DW MR imaging before and at 1, 2, and 3 months after antiandrogen therapy.
- Serum prostate-specific antigen (PSA) levels and mean ADCs of metastases were measured and analyzed.
- Functional DMs were used to evaluate per-voxel ADC changes.
Main Results:
- Serum PSA levels decreased by over 90% during therapy.
- Mean ADCs of bone metastases significantly increased at 1, 2, and 3 months post-treatment.
- Functional DM analysis revealed heterogeneous tumor responses, with varying proportions of voxels showing increased, unchanged, or decreased ADCs over time.
Conclusions:
- DW MR imaging is a viable tool for monitoring antiandrogen therapy response in prostate cancer bone metastases.
- Increased mean tumor ADC correlates with decreased PSA levels, indicating treatment efficacy.
- Functional DM analysis highlights the heterogeneity of tumor response to therapy at the voxel level.
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