Effect of neoadjuvant androgen deprivation therapy on prostate and tumor morphology prior to MRI-guided transurethral ultrasound ablation of prostate cancer
BACKGROUND: Thermal ablation is a minimally invasive treatment for localized prostate cancer (PCa). MRI-guided transurethral ultrasound ablation (TULSA) enables precise, temperature-controlled therapy, but its 3 cm ablation radius may limit coverage in large prostates or capsule-adjacent tumors. Neoadjuvant androgen deprivation therapy (nADT) may improve treatment feasibility by reducing prostate and tumor size. METHODS: In this prospective, single-arm pilot study (NCT05917860), 15 treatment-naïve patients with organ-confined, intermediate-risk ISUP 2-3 PCa and at least one biopsy-concordant PI-RADS ≥ 3 lesion received 3-month nADT with degarelix before whole-gland TULSA. Multiparametric MRI was performed at baseline and monthly thereafter to assess prostate and lesion volumes, tumor-capsule relationship, and urethra-capsule distance. RESULTS: < 0.001). Capsule bulging resolved in four of seven patients, and urethra-capsule distance decreased to ≤ 30 mm in all six patients with a baseline distance > 30 mm. CONCLUSION: Short-term nADT with degarelix was associated with significant changes in prostate and tumor morphology. Future studies should determine whether these changes improve TULSA outcomes.
Authors
- Teija Sainio (ORCID: https://orcid.org/0000-0001-5846-2601)
- Ilari Virtanen
- Mikael Anttinen (ORCID: https://orcid.org/0000-0002-9351-7177)
- Mikael Högerman (ORCID: https://orcid.org/0000-0002-4287-9231)
- Pertti Nurminen (ORCID: https://orcid.org/0000-0001-9364-9754)
- Pietari Mäkelä (ORCID: https://orcid.org/0000-0001-6224-0075)
- Otto Ettala
Institutions
- University of Turku (FI)
- Turku University Hospital (FI)
Publication Details
- Journal
- International Journal of Hyperthermia
- Published
- 2026-09-14
- DOI
- https://doi.org/10.1080/02656736.2026.2716351
- Primary Topic
- Prostate Cancer Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00