Medical technology company AngioDynamics Inc (NASDAQ: ANGO) reported on Wednesday that the two-year results from the PRESERVE pivotal trial of its NanoKnife System demonstrated sustained oncologic control and a consistent safety profile in patients with intermediate-risk prostate cancer.
The prospective, single-arm IDE study evaluated focal irreversible electroporation (IRE) in 121 patients with Gleason Grade Group 2-3 prostate cancer across 17 US clinical centres, in collaboration with the Society of Urologic Oncology Clinical Trials Consortium. Twelve-month results previously showed an 80% freedom-from-treatment-failure rate among protocol-biopsied patients, published in European Urology in July 2025.
At 24 months, 94.4% of analysis-eligible patients completed follow-up, with no new treatment failures reported among those assessed. One clinically indicated biopsy was negative for cancer, and 97% of patients recorded PSA levels below baseline. No new device- or procedure-related adverse events were observed between 12 and 24 months.
The findings reinforce longer-term international evidence supporting focal IRE as a treatment option designed to preserve quality of life while maintaining durable cancer control in intermediate-risk prostate cancer patients.
SOPHiA GENETICS and Synnovis partner to expand NHS liquid biopsy testing
AngioDynamics reports 24-month PRESERVE data showing durable NanoKnife outcomes in prostate cancer
Servier's Emi-Le receives US FDA breakthrough therapy designation for adenoid cystic carcinoma
Ranok Therapeutics reports positive Phase 1a clinical results for KRAS G12D inhibitor RNK08954
Anixa Biosciences reports extended survival signals in Phase 1 ovarian cancer CAR-T trial
Poolbeg Pharma secures Canadian patent grant for POLB 001
Harbour BioMed's HBM7004 receives US FDA IND clearance for Phase I trial
Innovent's IBI363 receives third Chinese regulatory BTD for MSS/pMMR CRC