About this trial
Today, the majority of clinically node positive (cN+) breast cancer patients is treated with neoadjuvant systemic therapy (NST). Axillary staging and treatment after NST in cN+ patients are areas of controversy. Patients with a pathological complete response (pCR) of the axillary lymph nodes are not expected to benefit from axillary lymph node dissection (ALND). Hence, less invasive axillary staging procedures are being introduced to avoid unnecessary ALND. However, evidence supporting the safety of replacing ALND by less invasive techniques in terms of oncologic safety and impact on quality of life (QoL) is lacking.
Eligibility criteria
Qualifiers
Female patient with unilateral invasive breast cancer and cN1-3
Pathologically proven positive axillary lymph node
Planned to undergo neoadjuvant chemotherapy (± immunotherapy), followed by staging and treatment of the breast and axilla
Disqualifiers
Clinically node negative breast cancer before NST
Bilateral invasive breast cancer
Neoadjuvant endocrine therapy
Distant metastases (including oligometastatic disease)
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Maastricht University Medical Center
Lead sponsor
Erasmus Medical Center
Collaborator
The Netherlands Cancer Institute
Collaborator