Evolving imaging methods of prostate cancer and the emergence of magnetic resonance imaging guided ablation techniques
- PMID: 36465377
- PMCID: PMC9714456
- DOI: 10.3389/fonc.2022.1043688
Evolving imaging methods of prostate cancer and the emergence of magnetic resonance imaging guided ablation techniques
Abstract
Established therapies for prostate cancer (PCa), surgery and radiotherapy, treat the entire gland regardless of the location of the cancerous lesion within the prostate. Although effective, these methods include a significant risk of worsening genitourinary outcomes. Targeted image-guided cancer therapy has gained acceptance through improved PCa detection, localization, and characterization by magnetic resonance imaging (MRI). Minimally-invasive ablative techniques aim to achieve comparable oncological outcomes to radical treatment while preserving genitourinary function. Transurethral ultrasound ablation (TULSA) and next-generation transrectal high-intensity focused ultrasound (HIFU) utilize MRI guidance to thermally ablate prostate tissue under real-time MRI monitoring and active temperature feedback control. Previous trials performed by our group and others, including a large multicenter study in men with localized favorable-risk disease, have demonstrated that TULSA provides effective prostate ablation with a favorable safety profile and low impact on quality of life. Recently, MRI-guided HIFU focal therapy was also shown as a safe and effective treatment of intermediate-risk PCa. Here we review the current literature on ablative techniques in the treatment of localized PCa with a focus on TULSA and HIFU methods.
Keywords: HIFU; MRI; Tulsa; ablation therapy; high-intensity focused ultrasound; magnetic resonance imaging; prostate cancer; transurethral ultrasound ablation.
Copyright © 2022 Anttinen, Blanco Sequeiros, Boström and Taimen.
Conflict of interest statement
MA reports grants from Profound Medical Inc, Finnish Urological Research Foundation, and Finnish Urological Association, and personal fees from Astellas, Bayer, Orion, and Janssen-Cilag, all outside the submitted work. PB reports personal fees from Profound Medical Inc and Janssen-Cilag Company outside the submitted work. PT reports personal fees from Roche, AstraZeneca, and MSD and non-financial support from MSD, all outside the submitted work. The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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