RecruitingNCT06700057

Clinical and Dosimetric Study of Patients Treated With 177Lu-PSMA-617 for Prostate Cancer.

Optimisation and Safety of an Innovative Nuclear Medicine Treatment: Clinical and Dosimetric Study of Patients Treated With 177Lu-PSMA-617 for Prostate Cancer.


Sponsor

Institut Bergonié

Enrollment

50 participants

Start Date

Nov 1, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Single-centre, retrospective and prospective observational study. This study aims to evaluate the dose delivered by radiation to the tumour and organs at risk, as a factor predicting response and the appearance of toxicities. Dosimetric calculations are made for each treatment using scintigraphic images acquired following injection of 177Lu-PSMA-617.


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria8

  • Patient aged 18 and over.
  • Patient with indication for or having started or completed treatment with 177Lu-PSMA-617 since 01/11/2023:
  • Progressive, metastatic, castration-resistant prostate cancer,
  • overexpressing prostate specific membrane antigen (PSMA)
  • treated with taxane chemotherapy and at least one 2nd generation hormone therapy (apalutamide, enzalutamide, darolutamide, abiraterone-prednisone).
  • Patient able to lie still for 1 hour for image acquisition.
  • Patient's place of residence \< 2 hours' drive from the Institut Bergonié.
  • Patient has not expressed any opposition to the use of his/her medical data for research purposes.

Exclusion Criteria1

  • None

Locations(1)

Institut Bergonie

Bordeaux, France

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NCT06700057


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