Aller au contenu
Retour à la recherche

NCT03408964Recrutement en cours

Valid Biomarkers in Blood to Predict the Response to Therapy in Prostate Cancer Patients

Résumé

Participants to the study will be assigned to 7 cohorts according to the stage of disease and planned antitumor treatment at time of study entry. In all patients, 12 ml of blood sample will be collected in EDTA tube for analysis of biological biomarkers in different time points.

Critères d'éligibilité

Inclusion Criteria: General inclusion criteria (for entering all groups) • Age ≥ 18 years • Histological diagnosis of prostate adenocarcinoma at different stages of disease (see Section 6.2) for which a treatment is indicated • Written Informed Consent Inclusion criterion only for entering Group 0 • Patients with a known diagnosis of CSPC or CRPC Inclusion criterion only for entering Group 1a • Patients that underwent biopsies for a suspect of PC, but resulted negative for cancer Exclusion Criteria: General exclusion criteria (for entering all groups) • Active infection requiring treatment • Decrease of general condition • Concomitant severe comorbities • Difficult socioeconomic conditions making regular follow up unfeasible. • Need of concomitant steroids at study entry and during the study • Diagnosis of second tumor in the previous 5 years Exclusion criterion only for entering Group 0 • No antibiotic treatments in the previous 2 months before enrollment Exclusion criteria only for entering Group 1 • Previous radical surgery and / or radical radiotherapy • Previous hormonal treatments Exclusion criteria only for entering Group 2 • No antibiotic treatments in the previous 2 months before enrollment (only in patients enrolling also for metagenomics and metabolomics) • Previous hormonal treatments for advanced disease Exclusion criterion only for entering Group 3 • No antibiotic treatments in the previous 2 months before enrollment (only in patients enrolling also for metagenomics and metabolomics analyses)

Contacts

Les coordonnées de l'équipe de l'essai s'affichent sur demande.

Voir la fiche officielle de l'essai
Statut
Recrutement en cours
Phase
—
Type d'étude
Observationnelle
Pays
Suisse
Promoteur
Oncology Institute of Southern Switzerland(Autre)
N° de protocole
IOSI-IOR-002
Pathologies
Prostate Cancer
Interventions
Autre

Traitements évalués

  • biological samples collection and analysis

Collaborateurs

Clinical Trial Unit Ente Ospedaliero Cantonale

Lieux · 1

  • Bellinzona, SuisseOncology Institute of Southern Switzerland (IOSI)Recrute dans ce centre

Au total, dans le monde, le seul centre listé au registre recrute.

Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 18 novembre 2025).

Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.

Voir aussi

Autres versions

Ces résultats sont indicatifs et ne remplacent pas un avis médical — à discuter avec votre médecin.