ARON-3 Study: International Multicentric Retrospective Study to Collect Global Experiences in the Treatment of Patients With Metastatic PCa

Last updated: June 28, 2024
Sponsor: Hospital of Macerata
Overall Status: Active - Recruiting

Phase

N/A

Condition

Prostate Cancer

Urologic Cancer

Prostate Cancer, Early, Recurrent

Treatment

N/A

Clinical Study ID

NCT06200558
ARON-3
  • Ages > 18
  • All Genders

Study Summary

Study wants to explore real-world data in three distinct settings

  • Patients with metachronous or de novo mCSPC treated with ADT+ARSI or ADT+ARSI+docetaxel _ARON-3S

  • Patients receiving Lutetium-177 PSMA for mCRPC _ ARON-3Lu

  • Patients treated with PARP inhibitors (alone or combined with ARSI) for CRPC _ ARON-3GEN

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients aged >18y

  • Cytological or Histologically confirmed diagnosis of PC

  • Histologically or radiologically confirmed diagnosis of metastatic disease and

For ARON-3S

▪ Treatment with ADT + Apalutamide or ADT + enzalutamide or ADT + Abiraterone or ADT + Abiraterone + Docetaxel or ADT + Darolutamide + Docetaxel (patients treated with previous docetaxel - CHAARTED - resulted eligible)

For ARON-3Lu

▪ Treatment with Luthetium-177-PSMA therapy for castration resistant PC

For ARON-3GEN

  • HRD POSITIVE STATUS

  • Treatment with PARP inhibitors for castration resistant PC. Treatment included:olaparib (as 1st, 2nd or 3rd line therapy), olaparib + abiraterone (as 1st linetherapy) or niraparib + abiraterone (as 1st line therapy) or talazoparib +enzalutamide

Exclusion

Exclusion Criteria:

  • Patients without histologically confirmed diagnosis of PC

  • Patients without histologically or radiologically confirmed metastatic disease and

For ARON-3S

▪ Patients treated with doublets or triplets not included in the list reported in the Inclusion Criteria Section

For ARON-3Lu

▪ Patients treated with Luthetium-177-PSMA therapy for hormone/castration sensitive PC

For ARON-3GEN

  • HRD NEGATIVE STATUS

  • Patients treated with PARP inhibitors alone or in combination regimens not includedin the ARON-3GEN study

Study Design

Total Participants: 534
Study Start date:
January 31, 2024
Estimated Completion Date:
December 31, 2025

Connect with a study center

  • Ospedale di Macerata

    Macerata, 62100
    Italy

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.