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Study identifier: NCT07370597 Synced from ClinicalTrials.gov · July 28, 2026
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LUtetium-177 DOsimetry as a Predictive Biomarker of Response in Metastatic Prostate Cancer Patients Treated With PSMA Radioligand THerapy.

Condition: Prostate Cancer (Adenocarcinoma)  ·  Sponsor: Jules Bordet Institute

PhaseN/A
Planned participants110
Who can joinMale, N/A to no upper limit
Healthy volunteersNo

About this study

A substantial proportion of patients with mCRPC do not respond to 177Lu-PSMA-RLT. The PSA response to Lu-PSMA was observed in nearly 46% of patients included in VISION trial and 66% in LuPSMA trial (4,5). The response to treatment can be evaluated after two cycles using the PSA or PSMA PET/CT scan. Gafita et al. Data have shown that PSA and PSMA perform equally in assessing response to 177Lu-PSMA treatment, and their changes after two cycles are related to patient survival. After two cycles, patients with no PSA or PSMA response had worse outcomes than those with partial response or stable disease . That means PSA and PSMA changes after two cycles can be used as a surrogate of patient outcome. However, the explanation of disease resistance to 177Lu-PSMA-RLT is not yet fully understood. Inappropriate dose administration might be one of the possible explanations. A dose-response relationship has been established in radiotherapy , making dosimetry a standard of care in conventional radiotherapy. In the radionuclide therapy settings, the dose-response relationship has been reported in a multi-center phase 2 trial on the selective internal radiotherapy in hepatocellular carcinoma. In this context, calculating the absorbed dose to tumour lesions could be an excellent method to individualize radionuclide therapy to achieve a maximal response to treatment. If dosimetry calculations could predict which patients would ultimately respond or not respond to treatment, administered dose an…

This description comes directly from the study's public registry record.

Talk to the study team

Carlos Artigas, MD  ·  02.54137.81  ·  carlos.artigas@hubruxelles.be

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Locations (1)

Institut Jules BordetBrussels, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT07370597