Darolutamide in Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexMale
Age18+
SponsorSwiss Cancer Institute

About this trial

Despite improvements in treatment, metastatic prostate cancer remains incurable, especially in the case of pretreated metastatic castration-resistant disease (mCRPC), where treatment options are limited, leading to an unmet need. The paradigm shift in the treatment of metastatic hormone-sensitive prostate cancer (mHSPC) has affected the treatment landscape for mCRPC patients. Many have already received androgen deprivation therapy (ADT) and androgen receptor pathway inhibitors (ARPI), making first-line mCRPC treatment challenging.

The Swiss Group for Clinical Cancer Research (SAKK) has shown in previous studies that maintenance treatment with an ARPI, such as darolutamide, can improve radiographic progression-free survival (rPFS) in pretreated mCRPC patients. In the SAKK 08/16 trial, darolutamide maintenance was found to prolong PFS compared to placebo, especially in patients who responded well to prior ARPI treatment.

Based on these findings, the hypothesis is that continued AR-pathway blockade with darolutamide, initiated in patients progressing from mHSPC to mCRPC on ARPI treatment, can improve outcomes when added to standard first-line mCRPC therapy and continued as maintenance. The proposed study aims to evaluate the efficacy of darolutamide, combined with physician-choice standard of care (including taxane chemotherapy, olaparib, radium 223, or LuPSMA), followed by maintenance therapy, on rPFS for patients in the first-line setting of mCRPC.

Eligibility criteria

Qualifiers

Written informed consent according to Swiss law and ICH GCP E6(R2) regulations before registration and prior to any trial specific procedures

Histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate

Castration resistance: tumor progression after orchiectomy or during treatment with GnRH analogues (agonists or antagonists).

Non-surgically castrated patient agrees on ongoing use of GnRH analogues (agonists or antagonists) during the trial

Disqualifiers

Presence of a small cell component

Prior systemic therapy for metastatic castration-resistant disease

Prior chemotherapy for mHSPC, except docetaxel

Prior LuPSMA or radium 223 for prostate cancer

Trial design

Treatments tested in this trial

  • Darolutamide
  • Standard of care

Treatment groups

162 Participants
are divided into 2 treatment groups

Sponsors and collaborators