Preoperative Accelerated Partial Breast Irradiation in Patients With Locally Recurrent or Second Primary Breast Cancer

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age51+
SponsorThe Netherlands Cancer Institute

About this trial

This study evaluates the acute toxicity and feasibility of repeat breast conserving therapy with preoperative accelerated partial breast re-irradiation (PAPBI) in female patients aged 51 years or older with ipsilateral recurrent or second primary low-risk breast cancer or DCIS.

Eligibility criteria

Qualifiers

Female patients ≥ 51 years

Ipsilateral breast cancer; recurrence or second primary

Either histologically proven invasive adenocarcinoma (invasive adenocarcinoma with DCIS component is also accepted) or DCIS alone (calcification associated on imaging)

Histologically proven estrogen receptor positive

Disqualifiers

≥ grade 3 radiotherapy toxicity in the breast after treatment of the primary tumor

Previous boost radiotherapy is not allowed, UNLESS the protocol tumor lies outside of the original boost area

Distant metastases and/or synchronous contralateral invasive or in situ carcinoma

Invasive lobular carcinoma (ILC) or pleiomorphic lobular carcinoma in situ (LCIS)

Trial design

Treatments tested in this trial

  • Preoperative accelerated partial breast irradiation
  • Breast conserving surgery
  • Sentinel node procedure
  • Biopsy track removal

Treatment groups

31 Participants
are divided into 1 treatment group

Sponsors and collaborators

The Netherlands Cancer Institute

Lead sponsor

Medical Center Haaglanden

Collaborator

Erasmus Medical Center

Collaborator