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utetium-177-PSMA in Oligo-metastatic Hormone Sensitive Prostate Cancer.

Phase 1
Recruiting
Conditions
prostate cancer
MedDRA version: 25.1Level: LLTClassification code: 10087976Term: Hormone-sensitive prostate cancer metastatic Class: 100000004848
Therapeutic area: Diseases [C] - Male Urogenital Diseases [C12]
Therapeutic area: Diseases [C] - Neoplasms [C04]
Registration Number
CTIS2023-509881-39-00
Lead Sponsor
Stichting Radboud University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
58
Inclusion Criteria

Histological proven adenocarcinoma of the prostate with sufficient archived tumor material. This material has to be archived till study closure, Laboratory values: • White blood cells > 3.0 x 109/l • Platelet count > 75 x 109/l • Hemoglobin > 6.2 mmol/l • ASAT, ALAT < 3 x ULN • MDRD-GFR = 50 ml/min, Signed informed consent, Biochemical recurrence (PSA > 1.0 µg/l), PSA-doubling time < 6 months. Serum PSA progression is defined as 2 consecutive rising PSA values measured at least 1 week apart. The minimal start value is 0.2 µg/l, 18F-PSMA-PET-CT positive metastases in bones and/or lymph nodes (N1/M1ab): =1, maximally 5 metastases, Local treatment for oligo-metastases with radiotherapy or surgery appears to be no option anymore (due to prior treatment or the location of the metastatic lesions or if the patient refuse these treatments), No prior hormonal therapy (including any androgen directed treatment such as finasteride, dutasteride, bicalutamide, apalutamide, abiraterone or enzalutamide) or taxane based chemotherapy (docetaxel or cabazitaxel); testosterone > 1.7 nmol/l. Exception: local prostate cancer treated with local radiotherapy plus adjuvant ADT; these patients need to be stopped with ADT at least 6 months, A detectable lesion on the 18F-PSMA PET/CT with significant PSMA avidity, defined by a SUVmax > 15 (partial volume corrected), ECOG 0-1, Patients must have a life expectancy >6 months

Exclusion Criteria

A known subtype other than prostate adenocarcinoma, Previous PSMA based radioligand treatment, Visceral or brain metastases, Any medical condition present that in the opinion of the investigator will affect patients’ clinical status when participating in this trial, Prior hip replacement surgery potentially influencing performance of PSMA PET/CT, Sjogren's syndrome, A second active malignancy other than prostate cancer, Patients who are sexually active and not willing/able to use medically acceptable forms of barrier contraception

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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