AXillary Surgery After NeoAdjuvant Treatment

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorEuropean Breast Cancer Research Association of Surgical Trialists

About this trial

The optimal surgical axillary staging technique in patients who convert from the clinically positive to clinically negative lymph node status under neoadjuvant therapy (cN+ → ycN0) remains to be clarified. Different strategies (axillary lymph node dissection, sentinel node biopsy, targeted axillary dissection) are currently used in different countries. A prospective analysis comparing these techniques regarding feasibility, safety, morbidity and surgical effort is urgently needed. Due to high complexity and discordant recommendations, a randomized trial comparing different techniques is hardly feasible. Therefore, the EUBREAST study group decided to initiate a prospective cohort study as an international project that aims at comparatively evaluating data on axillary staging after neoadjuvant therapy.

Eligibility criteria

Qualifiers

Signed informed consent form

Primary invasive breast cancer (confirmed by core biopsy)

cN+

cT1-4c

Disqualifiers

Distant metastasis

Recurrent breast cancer

Inflammatory breast cancer

Extramammary breast cancer

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators

European Breast Cancer Research Association of Surgical Trialists

Lead sponsor

AWOgyn

Collaborator

AGO-B

Collaborator

North Eastern German Society of Gynaecological Oncology

Collaborator

GBG Forschungs GmbH

Collaborator

Claudia von Schilling Foundation for Breast Cancer Research

Collaborator

Ehmann-Stiftung Savognin

Collaborator