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Recruiting

NCT Number: NCT06850545

Kuopio Lutetium-177 Study in Patients with PSMA-Positive Metastatic Prostate Cancer

KuPSMALu-trial is an observational study for patients treated with 177LuPSMA-I&T in Kuopio University Hospital, Finland. Study focuses on efficacy, safety and biomarker research.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Kuopio University Hospital

Kuopio, Northern Savonia, 70210, Finland

Location status: Recruiting

Location contact

Okko-Sakari Kääriäinen, MD

CONTACT

[email protected]

+358447179433

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The patient must sign informed consent to participate in the study.
  • Patients must be over 18 years of age.
  • Patients must have histologically confirmed metastatic prostate adenocarcinoma. Histological samples may show neuroendocrine features, but the primary component must be adenocarcinoma.
  • Patients must have metastatic castration-resistant prostate cancer (mCRPC) that has been treated with at least docetaxel and abiraterone or enzalutamide, or the patients must have declined chemotherapy or be ineligible for docetaxel-based chemotherapy due to contraindications.
  • Patients must have an adequate performance status: WHO 0-2.
  • Castration must have been achieved either chemically (LHRH analog or antagonist) or surgically (orchiectomy). Castration is defined as a low testosterone level (S-testosterone ≤ 1.7 mmol/l).
  • Patients must have PSMA-positive tumor burden detected by 18F-PSMA-PET-CT imaging.
  • Patients must have adequate renal and liver function (Creatinine < 2x upper limit of normal (ULN), ALT and ALP < 5x ULN).
  • Patients' blood counts must be within acceptable levels (Hb ≥ 100 g/l, Platelets ≥ 100 x 10⁹/L, Leukocytes ≥ 3.0 x 10⁹/L, or Neutrophils ≥ 1.0 x 10⁹/L).
  • The expected survival must be more than 6 months.
  • Patients with ejaculatory capacity must commit to not donating sperm during the treatments and for 6 months after treatment completion.

Exclusion criteria

  • Patients whose physical condition and cooperation are insufficient to follow the given instructions.
  • Patients who do not meet the criteria mentioned in the inclusion criteria.
  • Patients must not have PSMA-negative tumor burden in the liver. The amount of PSMA-negative tumor burden must not exceed the amount of PSMA-positive tumor burden.
  • Patients with symptomatic untreated spinal cord compression.
  • Patients must not have acute hydronephrosis or urinary tract obstruction.
  • Patients must not have a recurrent infection that impairs functional capacity.

Treatment and study plan

Primary outcomes

  1. Overall survival

    Time frame: 5 years

    Overall survival in the trial

Secondary outcomes

  1. PSA decrease of 50% or more

    Time frame: 36 weeks

    PSA decrease of 50% or more within the treatment period

  2. Adverse Events

    Time frame: 36 weeks

    Treatment-related grade ≥3 and serious adverse events

Study contacts

Contact information is provided by the study sponsor or research team.

Okko-Sakari Kääriäinen, MD

CONTACT

[email protected]

+358447179433

Sponsors and collaborators

Lead sponsor

Kuopio University Hospital

Other

Collaborators

  • University of Eastern Finland

Registry information

Acronym: KuPSMALu

Important dates

Study start
2020
Primary completion
2030
Study completion
2035
First posted
Feb 27, 2025
Registry last updated
Feb 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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