Actively Recruiting

Phase 2
Age: 50Years +
FEMALE
NCT06640881

Preoperative Partial Breast Reirradiation and Repeat Breast-conserving Surgery in Patients With Recurrent Breast Cancer: the REPEAT Trial

Led by Amsterdam UMC, location VUmc · Updated on 2025-10-01

25

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Over the past decades, interest in second breast-conserving therapy (BCT) has increased due to, among others, advancements in radiotherapy techniques. Preoperative partial breast irradiation (PBI) is an experimental treatment for patients with low-risk primary breast cancer. This approach can downstage the tumor, and may possibly reduce toxicity and improve cosmetic outcomes compared to postoperative radiotherapy. This study aims to evaluate the feasibility of single-dose preoperative PBI and second breast-conserving surgery (BCS) for patients with an ipsilateral recurrent breast event (IRBE) after previous BCT. The REPEAT trial is a multicenter, prospective, single-arm trial investigating ablative single-dose preoperative PBI in patients with an IRBE. Eligible patients are ≥ 50 years, have a unifocal non-lobular invasive breast cancer ≤ 2 cm, Bloom-Richardson grade 1 or 2, estrogen receptor-positive, HER2-negative and clinically negative axillary lymph nodes. The study plans to enroll 25 patients. Radiotherapy planning will involve the use of CT and MRI in the treatment position. Single-dose PBI of 20 Gy to the tumor and 15 Gy to the surrounding 2 cm of breast tissue will be delivered using a conventional or MR-guided linear accelerator. Tumor response will be monitored preoperatively using MRI and liquid biopsies to identify biomarkers for evaluating radiosensitivity. BCS will be performed 3 weeks post-PBI. The primary endpoint is the incidence of grade 2 or higher treatment-associated acute toxicity within 90 days. Secondary endpoints include the evaluation of acute (grade 1) and late toxicity, radiologic and pathologic response, mastectomy rate, patient-reported outcomes, cosmetic outcome, local, regional and distant recurrence rates, survival outcome, and biomarkers in liquid biopsies and tumor tissue. Patients will be followed up to 5 years after PBI. This trial will evaluate the feasibility of single-dose preoperative PBI and BCS for patients with IRBE. This treatment approach is expected to minimize the irradiated volume, reduce toxicity, and improve cosmetic outcomes compared to postoperative PBI after second BCS. Identifying biomarkers for radiosensitivity will help in selection patients and tailoring treatment.

CONDITIONS

Official Title

Preoperative Partial Breast Reirradiation and Repeat Breast-conserving Surgery in Patients With Recurrent Breast Cancer: the REPEAT Trial

Who Can Participate

Age: 50Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged 50 years or older with an ipsilateral invasive recurrent breast cancer after previous breast-conserving surgery and whole breast irradiation
  • World Health Organization performance status of 0 to 2
  • Tumor size 2 cm or less and unifocal on MRI
  • Tumor biopsy showing Bloom-Richardson grade 1 or 2, non-lobular invasive carcinoma, estrogen receptor positive, HER2 receptor negative, and no lymphovascular invasion
  • No extensive ductal carcinoma in situ (DCIS) outside the tumor area on mammography or biopsy, including non-mass enhancement on MRI
  • Clinically node-negative on 18-F FDG PET-CT, ultrasound, and MRI
  • No distant metastasis
  • No or mild late toxicity (no grade 2 or higher) from previous breast-conserving therapy
  • Adequate understanding of the Dutch language
Not Eligible

You will not qualify if you...

  • Ipsilateral invasive breast cancer event occurring less than two years after first breast-conserving therapy
  • Other malignancy within 5 years before the ipsilateral breast recurrence diagnosis (except carcinoma in situ)
  • Known breast cancer genetic mutation carrier
  • Presence of collagen synthesis diseases such as osteogenesis imperfecta, Ehlers-Danlos syndrome, or systemic sclerosis
  • Previous ipsilateral mastectomy
  • Invasive lobular carcinoma or ductal carcinoma in situ without invasive cancer
  • Absolute contraindications for MRI
  • Indication for treatment with neoadjuvant chemotherapy
  • Legal incapacity

AI-Screening

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC / VU Medical Centre

Amsterdam, Netherlands

Actively Recruiting

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Research Team

L

Lisca F Wurfbain, MD - PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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