Surgery may extend life in men with early bone metastases, major trial tests
NCT ID NCT02454543
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether removing the prostate and nearby lymph nodes, in addition to standard drug therapy, helps men with prostate cancer that has spread to a few bones live longer and delay the cancer becoming resistant to treatment. About 452 men with intermediate- or high-risk prostate cancer and limited bone metastases are being followed for up to 10 years. The goal is to see if the combination approach improves cancer-specific survival and quality of life compared to drug therapy alone.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 452 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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May 2015
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Patients with locally resectable intermediate and high-risk prostate cancer which has been confirmed by biopsy according to D'Amico criteria (intermediate risk: PSA 10-20 ng/ml, cT2b-c, Gleason score 7; high risk: PSA \>20 ng/ml, \>cT2c, Gleason score 8-10) with clinical evidence of bone metastases in imaging tests can be included. Necessary radiotherapy of the bone metastases as required is also permitted prior to inclusion in the study. In line with the results from the recent CHAARTED and STAMPEDE studies (Sweeny et al., 2015, James et al 2015), early treatment with taxanes may be used in both the standard treatment arm as well as in the intervention arm where the prostatektomie is performed. The period 6 months from the initial diagnosis to randomization and possibly three months from randomization to surgery must be complied with. Inclusion criteria 1. Patients with newly diagnosed prostate cancer which has been confirmed by histological examination (within the last 6 months prior to randomization) 2. At least one and at most 5 bone metastases in imaging tests (bone scintigraphy, CT, MRT or PET) at diagnosis with no evidence of visceral metastasis. Patients with evidence of lymph node metastasis (N1) are allowed 3. PSA ≤ 200 ng/ml at diagnosis (without ADT) 4. Asymptomatic or mild symptomatic disease 5. Locally resectable tumour stage 6. ECOG Performance Score 0-1 7. Submission of the patient's written declaration of informed consent following explanation 8. Age ≥ 18 - ≤ 75 years 9. Full legal capacity and compliance of the Patient Exclusion Criteria: * Contraindications to radical prostatectomy (Local non-resectable disease, increased anesthetic risk due to comorbidities) * Detection of more than 5 bone metastases * Pain management with opioid analgetics * Evidence of visceral metastases or brain metastases * Neuroendocrine and / or small cell differentiation in histology of the biopsy * Charlson Comorbidity Index \> 2 * ECOG Performance Score \> 1 * Myocardial infarction or stroke within the last 6 months * Existing major cardiovascular (grade III - IV according to NYHA), pulmonary (pO2 \<60 mmHg), renal, hepatic or hematopoietic disease (e.g. severe bone marrow aplasia) * Severe psychiatric disorders persons housed on judicial or administrative arrangement in an institution * Simultaneous participation in another clinical trial with interventional character of the metastatic prostate cancer
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Markus Graefen
Hamburg, Nein, 20246, Germany
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Other studies related to the condition(s) this trial covers.
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