← Eichor
Study identifier: NCT07686016 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prostate Radiotherapy and Metastasis-Directed Therapy in Synchronous Oligometastatic Prostate Cancer

Condition: Prostate Cancer · Metastatic Prostate Cancer · Oligometastatic Prostate Cancer  ·  Sponsor: Affidea Nu-med Center of Oncological DIagnostics and Therapy

PhaseN/A
Planned participants700
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is an ambispective, multicenter, observational real-world registry of patients with synchronous de novo oligometastatic prostate cancer, defined as prostate cancer with up to 10 extraregional metastatic lesions diagnosed at initial presentation or within 6 months of the primary diagnosis. The study will evaluate outcomes after comprehensive local and metastasis-directed treatment. Eligible patients receive definitive prostate-directed radiotherapy, which may include external-beam radiotherapy, external-beam radiotherapy with brachytherapy boost, or definitive prostate brachytherapy monotherapy in selected patients, together with stereotactic body radiotherapy to all identified extraregional metastatic lesions. Systemic therapy is given according to routine clinical practice and local multidisciplinary decisions. The registry is non-interventional. Participants are not assigned to treatment by the study protocol, and no experimental treatment, randomization, or protocol-mandated imaging schedule is used. The study collects de-identified data from routine medical records, including baseline disease characteristics, imaging, radiotherapy details, systemic therapy, radiographic progression, patterns of failure, subsequent treatments, adverse events, and survival. The study includes historical retrospective data, prospective follow-up of previously treated eligible patients, and prospective enrollment of newly eligible patients from the registry activation date. The main g…

This description comes directly from the study's public registry record.

Talk to the study team

Mateusz Bilski, MD, PhD  ·  81 536 04 50  ·  mateusz.bilski@affidea.com

Paulina Kleban  ·  81 536 04 50  ·  paulina.kleban@affidea.com

Always discuss trial participation with your own doctor first.

Locations (1)

Affidea Nu-med Center of Oncological Diagnostics and TherapyZamość, Lublin Voivodeship, PolandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07686016