About this trial
Women at high risk of breast cancer (BC) should undergo annual magnetic resonance imaging (MRI) and digital mammography (DM) from at least ages 35 to 60. While MRI is an expensive and scarce resource, contrast-enhanced mammography (CEM) is a less costly and time-consuming alternative that could be used to screen these women instead of MRI. The Con-TRUST trial aims to randomize 1400 women in 10 centers to test whether CEM can be used instead of MRI+DM for BC detection in high-risk women (\>5% 5-year BC risk). The study will compare efficacy in reducing the incidence of BC in women who tested negative in the first screening and cumulative recall rates over 2 screening rounds. All women will be followed up for 2.5 years. Secondary outcomes include screening performance, safety, and women\'s compliance. The trial results will be integrated with the international literature and proposed for the development of recommendations as part of the adolopment of European guidelines in Italy.
Eligibility criteria
Qualifiers
Women at high risk of developing breast cancer already in care at participating centers or new referral for early diagnosis programs, aged between 35 and 60 years, with an estimated risk of breast cancer in the next 5 years >=5%.
Tyrer Cuzick IBIS: criterion >10% at 10 years;
BOADICEA: criterion >10% at 10 years;
BCSC: criterion >10% at 10 years (if possible switch to Tyrer-Cuzick if >=2 relatives with breast or ovarian cancer);
Disqualifiers
- Previous breast cancer;
Pregnancy;
Bilateral mastectomy;
Psychiatric or other disorders not compatible with compliance with the protocol and follow-up requirements;
Trial design
Treatments tested in this trial
- Contrast Enhancement Mammography
- magnetic resonance imaging (MRI) and digital mammography (DM)
Treatment groups
Sponsors and collaborators
Azienda USL Reggio Emilia - IRCCS
Lead sponsor
Istituto Oncologico Veneto I.O.V. - I.R.C.C.S.
Collaborator
Azienda Ospedaliera Universitaria Policlinico "G. Martino"
Collaborator
Azienda Ospedaliera Universitaria (AOU) Bari
Collaborator
Azienda Ospedaliera Universitaria Integrata Verona
Collaborator
Fondazione IRCCS Policlinico San Matteo di Pavia
Collaborator
Azienda Ospedaliero-Universitaria di Modena
Collaborator
Azienda USL della Romagna
Collaborator
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
Collaborator