Tb-PSMA-I&T Radionuclide Before Radical Prostatectomy in Patients With Locally Advanced Prostate Cancer - TbeforePROST Trial.

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexMale
Age18+
SponsorRabin Medical Center

About this trial

This is a multi-disciplinary collaboration between urologists, oncologists and nuclear medicine physicians from Beilinson hospital at Rabin Medical Center to address the major therapeutic challenge of locally advanced prostate cancer. Our aim is to evaluate the use of a novel treatment (Tb-PSMA) prior to the surgical removal of the prostate. This treatment has already shown initial promising results in patients with metastatic prostate cancer but has never been tested for locally advanced disease before surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male aged 18 years and older.

Patients with high-risk localized prostate cancer (cT3/4 and/or Gleason score ≥ eight and/or prostate biopsy or PSA ≥ 20 ng/dl)

High PSMA expression was confirmed according to PROMISE V2 8

Patients should have an Eastern Cooperative Oncology Group (ECOG) performance status score of 1 or lower and a life expectancy of > 10 years.

Disqualifiers

Platelet count lower than 150×103/µl

white blood cell count lower than 4×103/µl,

haemoglobin concentration lower than 12mg/dl.

albumin concentration lower than 3.5 g/dl.

Trial design

Design model

Single group

Treatments tested in this trial

  • Tb-PSMA-I&T (Tb-PSMA)

    Drug

    Terbium-161 produce beta emission with the addition of Auger electrons which have higher linear energy transfer and a very short range. By that it has the potential to improve local and distal (micro-metastatic disease) efficacy with a similar safety profile. It will be given to patients with high risk locally advanced prostate cancer prior to Radical prostatectomy

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Patients receiving Tb-PSMA before RAdical prostatectomyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Number of Tb-PSMA adverse effects measured by CTCAE v4.0 and number of surgical complications - measured by the Clavien-Dindo Classification (2009)

Time frame
1 year
2

Surgical and clinical safety

The primary outcome is the safety of administering Tb-PSMA before radical prostatectomy, its impact on intra- and post-operative clinical course according to the Clavien-Dindo Classification.

Time frame
1 year

Secondary outcomes

1

Immediate oncological outcomes as measured by number of patients with positive surgical margins and number of patients who achieved biochemical complete response

Secondary outcomes include the immediate response to treatment in terms of biochemical response. A post-surgical prostate specific antigen above 0.1 ng/ml is considered biochemical failure.

Time frame
3 months

Other outcomes

Sponsors and contacts

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