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Active Not RecruitingNCT04461808

Tomosynthesis as Primary Test for Breast Cancer Screening

Tomosynthesis as Primary Test for Breast Cancer Screening: A Multicenter Randomized Controlled Trial

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
10,156 (actual)
Sponsor
Azienda USL Reggio Emilia - IRCCS · Other Government
Sex
Female
Age
45 Years – 65 Years
Healthy volunteers
Accepted

Summary

Randomized trial comparing tomosynthesis plus synthetic 2D Mammography vs Digital Mammography in respect to incidence of advanced cancers (interval and following round) and interval cancers.

Detailed description

This is a companion study of the other Italian studies on tomosyntesis as primary screening test for breast cancer: RETomo (NCT02698202), PROTEUS (NCT02590315), IMPETO (NCT03587259). The investigators conduct a randomized trial in three centres with a protocol that is similar to that of the other three studies. As for IMPETO and differently from the RETomo and PROTEUS studies, the intervention will be tomosynthesis + synthetic 2D. In the three centres about 8000 women will be recruited (4000 in the experimental arm and 4000 in the control arm). The study will compare the performance of tomosynthesis plus synthetic 2D vs digital mammography in respect to incidence of advanced cancers (interval and following round) and interval cancers. Women 50 to 65 years old will be screened once according to randomization arm for one round, then all will be screened with digital mammography after two years. The investigators also will measure detection rates, specificity, interval cancers, advanced cancers occurring as interval cancers or at subsequent screens and allowing to estimate excess overdiagnosis comparing overall cumulative incidence after two or three rounds of screening. Women will be asked for informed consent when they attend the mammography. If they accept they will be randomised to one of the two arms. All examinations will be read by two independent radiologists, in case of discordance a third reading is asked.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTtomosynthesis + synthetic 2DWomen will be screened for one round with tomosynthesis + synthetic 2D, two projections, double reading with consensus or arbitration, according to local protocols, for discordant readings. After two years (one years for women 45-49 yo) women will be re-screened with digital mammography.
DIAGNOSTIC_TESTdigital mammographyWomen will be screened for one round digital mammography, two projections, double reading with consensus or arbitration, according to local protocols, for discordant readings. After two years (one years for women 45-49 yo) women will be re-screened with digital mammography.

Timeline

Start date
2019-07-15
Primary completion
2027-04-30
Completion
2029-04-30
First posted
2020-07-08
Last updated
2025-06-25

Locations

4 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT04461808. Inclusion in this directory is not an endorsement.