Laurence Klotz, Stefan Grudén, Niklas Axén, Charlotta Gauffin, Cecilia Wassberg, Anders Bjartell, Jonathan Giddens, Peter Incze, Kenneth Jansz, Mindaugas Jievaltas, Ricardo Rendon, Patrick O Richard, Albertas Ulys, Teuvo L Tammela
Journal: European urology focus 2022;8(1):112-120
PMID: 33583762
BACKGROUND
There is increasing interest in nonmorbid treatments for low- and intermediate-risk prostate cancer with fewer side effects than surgery or radiotherapy.
OBJECTIVE
To investigate the tolerability, safety, and antitumor effects of the intraprostatic NanoZolid depot formulation Liproca Depot (LIDDS AB, Uppsala, Sweden) with antiandrogen 2-hydroxyflutamide (2-HOF) in men with low- or intermediate-risk localized prostate cancer managed with active surveillance.
DESIGN, SETTING, AND PARTICIPANTS
This clinical phase 2b trial, LPC-004, involved 61 patients. The 2-HOF-containing formulation Liproca Depot was injected transrectally into the prostate under ultrasound guidance. A single dose of 35% or 45% of the prostate volume (study part 1) and a fixed dose of 16 or 20 ml (study part 2) of the formulation were evaluated.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSES
The primary endpoints were tolerability and the reduction in serum prostate-specific antigen (PSA) 5 mo after injection. Antitumor effects were evaluated with magnetic resonance imaging (MRI) and prostate biopsies. Quality of life was assessed using a validated questionnaire (International Prostate Symptom Score).
RESULTS AND LIMITATIONS
All doses were safe and well tolerated, without hormonal side effects. In part 2 of the study, the PSA reduction was greatest for the group receiving 16 ml, with an average decrease of 14%, and 95% of patients had a PSA reduction. Some 78% of patients showed a prostate volume decrease compared to baseline. Prostate MRI and biopsies confirmed stable or reduced lesion size. However, post treatment biopsies were performed at the discretion of the investigator, and not routinely. Most patients were amenable to a second injection.
CONCLUSIONS
PSA and prostate volume decreased in most patients. Indications of efficacy were shown by post-treatment MRI and biopsies demonstrating stabilization or regression in the majority of cases.
PATIENT SUMMARY
Liproca Depot is a safe, minimally invasive treatment that offers the potential for cancer control in patients with intermediate-risk prostate cancer. Further clinical evaluation is warranted.
Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.
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