Development of the PRIME Test for the Identification of Prostate Cancer Patients' Biomarkers Through Non-invasive Liquid Biopsies

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of prostate cancer

• Eligible for prostate cancer pharmacological treatment

• Given consent to study participation

Locations
Other Locations
Italy
Istituto Romagnolo per lo Studio dei Tumori
RECRUITING
Meldola
Azienda Ospedaliera San Luigi
RECRUITING
Orbassano
Istituto Oncologico Veneto
RECRUITING
Padua
Santa Chiara Hospital
RECRUITING
Trento
Contact Information
Primary
Orazio Caffo
orazio.caffo@apss.tn.it
+39 0461902121
Time Frame
Start Date: 2019-05-07
Estimated Completion Date: 2027-01-31
Participants
Target number of participants: 800
Treatments
Metastatic Castration Resistant Prostate Cancer (mCRPC) patients
This group includes mCRPC patients treated with serial lines of treatment.~For each line of treatment, blood samples are collected:~1. Before starting the treatment;~2. After 12 weeks;~3. At the end of the treatment/progression.
Metastatic Hormon Sensitive Prostate Cancer (mHSPC) patients
This group includes mHSPC patients treated with hormone therapy.~In the hormone sensitive setting, blood samples are collected:~1. Before starting the treatment;~2. After 12 weeks;~3. Every six months until progression to the castration resistant status.
Related Therapeutic Areas
Sponsors
Leads: Santa Chiara Hospital
Collaborators: Università degli Studi di Trento

This content was sourced from clinicaltrials.gov