#0955
Australian, multi-centre assessment of Focal Laser Ablation with ProFocal® in Localised Prostate Cancer
Y. Bushati1,2, J. Kam1,3,2, B. Canagasingham1,3, A. Goolam1,3,4, A. Hadley5, M. Winter1,3, M. Khadra1,3,2, N. Mehan1,3, I. Thangasamy1,3,2, C. Varol1,3,6
1Nepean
Urology Research Group, Kingswood, Australia
2University of Sydney, Sydney Medical School, Sydney, Australia
3Nepean Hospital, Kingswood, Australia
4Sydney Adventist Hospital, Wahroonga, Australia
5Mater Private Hospital, Redland, Australia
6Medlogical Innovations, Sydney, Australia
Introduction:
Focal laser ablation (FLA) is an emerging, minimally invasive treatment for localised prostate cancer. ProFocal® device (Medlogical Innovations, Sydney, Australia) is a novel, cooled, focal laser ablation device for prostate cancer with the pivotal PFLT-PC study completed in 2023. We aimed to assess the real-world oncological outcomes in patients undergoing FLA with the ProFocal® device.
Material and methods:
Following the completion of the PFLT-PC trial, we established a prospective database tracking patients treated with the ProFocal® device across four institutions in Australia. Inclusion criteria were PSA ≤15 ng/mL, clinical stage ≤T2c, ISUP 2–3, and one or two MRI-visible lesions concordant with biopsy findings. Treatment success was assessed by transperineal biopsy at 3 months post-procedure.
Results:
The data from 87 patients with a total of 97 MRI-biopsy concordant lesions were analysed. The median age was 67 years (IQR 62–74), PSA 6.0 ng/mL (IQR 4.1–7.1), prostate volume 42cc (IQR 32–57) and MRI lesion volume 0.90cc (IQR 0.5 – 1.35). All cases were completed as day only procedures. Median treatment duration was 57.4 minutes (IQR 45–75), involving a median of 8 ablations (IQR 7–10) across 4 locations (IQR 3–5). PSA significantly decreased at 3 months, with a median reduction of 1.05 ng/mL (IQR 0.0–3.4; p < 0.001). Follow-up biopsies identified residual cancer (ISUP ≥2) in 17 of the patients. Four patients with infield residual cancer also had ISUP ≥2 in their outfield biopsies, thus overall true treatment failure occurred in 15% of patients.