PRostate Cancer Plasma Integrative Multi-modal Evaluation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorSanta Chiara Hospital

About this trial

The study aims to develop PRIME (PRostate cancer plasma Integrative Multi-modal Evaluation) liquid biopsy test and to implement its use to query prospectively collected samples in advanced prostate cancer (PCa) clinical trials and/or clinical settings. In order to maximise the utility of liquid biopsies for advanced PCa, PRIME is focused on the development of novel computational and sequencing approaches that integrate multiple information from plasma circulating elements: i) cell free DNA (cfDNA) gene mutation data with accurate quantitation of cfDNA structural genomic changes, ii) cfDNA genomic profiling with cfDNA methylation status, and iii) the information provided by extracellular vesicles (EVs) and EV-associated cargo (including DNA, RNA and proteins).

Eligibility criteria

Qualifiers

Diagnosis of prostate cancer

Eligible for prostate cancer pharmacological treatment

Given consent to study participation

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Analysis of cell free DNA, and extracellular vesicles (EVs) and EV-associated molecular components (including RNA, DNA, proteins)

Treatment groups

800 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Santa Chiara Hospital

Lead sponsor

Università degli Studi di Trento

Collaborator