Evaluating Omitting of Internal Mammary Irradiation Among Early Stage Intermediate Risk (N1) Breast Cancer

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-80
SponsorRuijin Hospital

About this trial

The effect of internal mammary irradiation (IMI) added to whole-breast or thoracic-wall irradiation plus supraclavicular (SVC) irradiation after surgery on survival among women with early-stage intermediate risk (N1) breast cancer remains debated. The present study aimed to identified patient could be omitted from internal mammary lymph node irradiation by using a clinical-genomic model.

Eligibility criteria

Qualifiers

• Histologically confirmed invasive breast cancer

Underwent radical surgery with either mastectomy or breast conserving surgery and axillary lymph node dissection (ALND)

The number of positive lymph node should be 1-3 (N1).

Clinical high risk breast cancer (≥2 clinical risk factors)

Disqualifiers

• Axillary dissection of less than 10 lymph nodes

Pathologically positive ipsilateral supraclavicular lymph node

Pathologically or radiologically confirmed involvement of ipsilateral internal mammary lymph nodes

Pregnant or lactating women

Trial design

Treatments tested in this trial

  • omit of IMI group
  • IMI group

Treatment groups

214 Participants
are divided into 2 treatment groups

Sponsors and collaborators