Key result
Residual fiducial markers permit successful TULSA thermal dosing in ~70% of cases despite specific disruptions.
Why the study?
Residual fiducial markers from prior external beam radiation therapy may compromise subsequent MR-guided transurethral ultrasound ablation by causing ultrasound field distortions and susceptibility artifacts.
How do residual fiducial markers affect the ablation outcome during clinical TULSA treatments in patients with radiorecurrent prostate cancer?
Observational (n=9)
How do residual fiducial markers affect the ablation outcome during clinical TULSA treatments in patients with radiorecurrent prostate cancer?
Marker composition, orientation, and location inside the prostate can impact TULSA treatment outcomes, highlighting the need for detailed MRI screening for patient selection.
Residual fiducial markers may impair TULSA heating by type and position; supports MRI screening but leaves open prospective validation.
OBJECTIVES: Fiducial markers improve accuracy in external beam radiation therapy (EBRT) for treatment of prostate cancer (PCa). However, many patients recur after EBRT necessitating additional treatment, such as MR-guided transurethral ultrasound ablation (TULSA). Residual markers may compromise TULSA through ultrasound field distortions and generation of local susceptibility artifacts. The objective was to investigate how markers affect the ablation outcome during clinical TULSA treatments. SUBJECTS AND METHODS: A retrospective analysis was performed on nine patients with radiorecurrent PCa and residual markers who received TULSA. The MR susceptibility artifact was quantified as a function of marker type, size and orientation, in particular for thermometry. The spatial distribution of markers inside the prostate was recorded, and the resulting impact on the thermal dose was measured. The thermal dose measurements were directly compared to the residual enhancing prostatic tissue observed on the immediate and control post-TULSA contrast enhanced (CE) image. RESULTS: Successful thermal dose accumulation to the target boundary occurred for 14/20 (70%) of markers, confirmed with CE imaging. Gold markers situated simultaneously close to the urethra (≤12 mm) and far from the target boundary (≥13 mm) reduced the ultrasound depth of heating. Nitinol markers produced large, hypointense artifacts that disrupted thermometry and compromised treatment. Artifacts from gold markers were less pronounced, but when located near the target boundary, also affected treatment. CONCLUSION: Marker composition, orientation and location inside the prostate can all potentially impact treatment outcome. Proper patient selection through detailed MRI screening is critical to ensure successful radiorecurrent PCa treatment outcomes with TULSA.
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A 2021 study conducted an observational in Radiorecurrent prostate cancer (n=9). Residual fiducial markers was evaluated on Successful thermal dose accumulation to the target boundary. Residual fiducial markers allowed successful thermal dose accumulation to the target boundary in 70% (14/20) of cases during TULSA, though nitinol and specific gold markers disrupted treatment.
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