aPBI Re-irradiation

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age40+
SponsorDartmouth-Hitchcock Medical Center

About this trial

This study is to determine whether acute treatment-associated adverse events following breast re-irradiation with aPBI are acceptably low and to assess local control following breast re-irradiation with aPBI. An exploratory aim is to assess cosmetic outcomes following breast re-irradiation with aPBI.

Eligibility criteria

Qualifiers

Patients who have histologically-confirmed, second, ipsilateral breast cancer which was diagnosed more than one year after completing breast conserving therapy.

Patients must have received prior radiotherapy to the breast

Patients must have an intact, involved breast.

Patients must meet ASTRO 2023 guidelines for a strong recommendation for partial breast irradiation.

Disqualifiers

Patients who have not received prior radiotherapy to the ipsilateral breast.

Patients who do not meet ASTRO 2023 guidelines for a strong recommendation for partial breast irradiation, including those who meet criteria for conditionally recommended, conditionally not recommended, and not recommended for partial breast irradiation.

Patients who are < 40 years of age.

Patients with breast implants or other breast reconstruction.

Trial design

Treatments tested in this trial

  • Reirradiation

Treatment groups

30 Participants
are divided into 1 treatment group