A Study of Biological, Genetic, and Constitutional Factors and Non-invasive Monitoring to Assess Personal Cancer Risks
Recruiting · NCT07469709 · Observational (researchers observe without assigning treatment) · Lead sponsor: Fondazione del Piemonte per l'Oncologia
View the official record on ClinicalTrials.gov →What this trial is about
The PRO-ACTIVE study aims to develop a clinical-translational program in the field of cancer prevention in all its phases (primary, secondary, and tertiary) to intervene before the clinical and radiological manifestation of the disease. It starts with risk prediction and leads to early diagnosis of the disease or recurrence in the subclinical phase. The PRO-ACTIVE study includes the following activities: * WP1: Integrated DNA-RNA approach for the identification of hereditary markers of predisposition to tumors * WP2: Global biological and molecular analysis of the host and tumor for the prevention and monitoring of recurrences * WP3: Analysis of the immunological status for the diagnosis of primary prevention and relapses in correlation to genetic and environmental factors * WP4: Study of the tumor microenvironment for recurrence prediction
Who can take part
Inclusion criteria
- Age \>18 years;
- Patients with breast cancer, including patients who meet the AIOM criteria for eligibility for BRCA testing and patients with lobular breast cancer;
- Patients with radically resected colon cancer, including patients with stage III colon cancer and vascular invasion;
- Patients with ovarian carcinomas;
- Patients with metastatic melanoma;
- Patients with stage IIB and IIIA non-small cell lung cancer.
Exclusion criteria
- Age \<18 years;
- Unwillingness or inability to give informed consent
Where it is running
1 location listed.
- Fondazione del Piemonte per l'Oncologia-IRCCS Candiolo - Candiolo, Turin, Italy