Surgical Excision vs Neoadjuvant Radiotherapy+Delayed Surgical Excision of Ductal Carcinoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorStanford University

About this trial

The purpose of this pilot study is to compare by pathological findings surgical excision versus neoadjuvant radiotherapy followed by delayed surgical excision of ductal carcinoma in situ (DCIS)

Eligibility criteria

Qualifiers

Core needle biopsy demonstrating DCIS (ductal carcinoma in situ) of non-palpable, image-detected breast abnormality

Signed and dated IRB-approved written informed consent

Women 18 years of age or older

Mammographic calcifications or MRI non-mass enhancement measuring 4 cm or less in greatest dimension, including multifocal disease

Disqualifiers

Invasive carcinoma on core needle biopsy, including microinvasive carcinoma

Radiographic extent of DCIS >4.0 cm

Mass lesion on breast imaging or palpable tumor

No residual radiographic lesion after diagnostic percutaneous core needle biopsy

Trial design

Treatments tested in this trial

  • Lumpectomy
  • Partial breast irradiation prior to surgery

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators