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Study identifier: NCT06600802 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intrinsic Validity of Molecular Marker(s) Detection on Tissular Tumoral DNA to Predict the Efficacy of 177Lutetium-PSMA-617 (Lu-PSMA) Treatment for Castration-resistant Metastatic Prostate Cancer

Condition: Castration-resistant Metastatic Prostate Cancer · Treated by 177Lutetium-PSMA-617 (Lu-PSMA)  ·  Sponsor: Centre Jean Perrin

PhaseNA
Planned participants120
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Prostate cancer is the most common cancer in men. Its incidence is rising as the population ages. In the localized stage, the 5-year overall survival rate (OS) is 98%. Metastatic progression and resistance to castration have a negative impact on prognosis. Despite recent advances in management, the 5-year OS is around 30%. Therapeutic advances in this indication have been made mainly by the use of taxanes and second-generation hormone therapy. These treatments have improved OS and progression-free survival (PFS). They are now used as standard therapy. More recently, the Phase III VISION trial confirmed the improvement in OS and radiological PFS achieved by treatment with the radioligand 177Lutetium-PSMA-617 (Lu-PSMA) in patients with advanced metastatic castration-resistant prostate cancer (mCRPC). This treatment is currently available in early access in France. Despite encouraging results, 40% of patients will not respond to Lu-PSMA, and there are currently no validated predictive factors. Studies are currently on going, but the identification of biomarkers seems necessary to better stratify risk in these patients. Numerous tissue prognostic tests based on molecular characteristics or cell proliferation are emerging with this in mind. At present, molecular profiling is not a routine technique for prostate cancer, as it is for other solid cancers. At an early stage, the Decipher® Genomic classification tool has shown prognostic utility independently of therapeutic and clin…

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

Talk to the study team

Judith PASSILDAS JAHANMOHAN, PhD  ·  0473278005  ·  judith.passildas@clermont.unicancer.fr

Always discuss trial participation with your own doctor first.

Locations (5)

Centre Jean PERRINClermont-Ferrand, FranceRecruiting
CHU de GrenobleLa Tronche, FranceNot Yet Recruiting
Hospices Civiles de LyonPierre-Bénite, FranceNot Yet Recruiting
Hôpital privé de la LoireSaint-Etienne, FranceNot Yet Recruiting
Centre Paul STRAUSSStrasbourg, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06600802