IRIS: Risk-Based Imaging After Breast-Conserving Surgery

ConditionBreast Cancer
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUmeå University

About this trial

Breast cancer follow-up after curative treatment is currently based on largely uniform imaging surveillance strategies, despite substantial variation in recurrence risk across patient subgroups. Early detection of recurrences improves prognosis, particularly when detected by imaging rather than symptoms, but the optimal surveillance approach remains uncertain. Mammographic sensitivity is lower in breast cancer survivors than in screening populations, and interval cancers occur more frequently, especially among younger patients, those with dense breasts, aggressive tumor subtypes, or without radiotherapy after breast-conserving surgery.

This multicenter, open-label, register-based randomized controlled trial evaluates risk-stratified imaging surveillance after breast-conserving surgery for breast cancer. The study investigates whether more sensitive imaging methods, compared with standard mammographic follow-up, lead to earlier detection of ipsilateral recurrences and contralateral second primary breast cancers in patients at increased risk of recurrence.

The primary endpoint is the number of interval ipsilateral recurrences and contralateral second primary breast cancers detected within five years from index diagnosis. Secondary endpoints include stage at detection, breast cancer-specific survival, overall survival, recall rate, biopsy rate, false positive findings, and health-related quality of life.

Eligibility criteria

Qualifiers

Histologically confirmed primary breast cancer

Treated with breast-conserving surgery with curative intent

Completed primary treatment according to clinical guidelines

Classified as having increased risk of recurrence according to predefined study risk criteria (based on factors such as age, tumor subtype)

Disqualifiers

Previous ipsilateral or contralateral invasive breast cancer within the last 5 years (except index cancer)

Bilateral mastectomy

Known metastatic breast cancer at time of enrollment

Contraindication to contrast agents or MRI (if applicable for assigned arm)

Trial design

Treatments tested in this trial

  • Risk-Stratified Imaging Surveillance
  • Standard Mammographic Surveillance

Treatment groups

2,300 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators