Liproca Depot: A New Antiandrogen Treatment for Active Surveillance Patients.

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

Abstract

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.

Address: Division of Urology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.; Department of Laboratory Medicine, Karolinska Institutet, Huddinge, Sweden; LIDDS AB, Uppsala, Sweden. Electronic address: [email protected].; LIDDS AB, Uppsala, Sweden.; Radiology Department, Karolinska Universitetssjukhuset, Stockholm, Sweden.; Department of Translational Medicine, Skåne University Hospital, Malmö, Sweden.; Medicine Professional Corp, Brampton, Canada.; Oakville Trafalgar Memorial Hospital, Oakville, Canada.; Burlington Professional Centre, Burlington, Canada.; Hospital of Lithuanian University of Health Sciences Kauno Klinikos, Kaunas, Lithuania.; Centre of Applied Urology Research, Halifax, Canada.; Centre Hospitalier Universitaire de Sherbrooke and CHUS Research Centre, Sherbrooke, Canada.; National Cancer Institute, Vilnius, Lithuania.; Tampere University Hospital and Tampere University, Tampere, Finland.
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