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Study identifier: NCT05462457 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

TAD in Primary Breast Cancer With Initially ≥ 3 Suspicious Lymph Nodes

Condition: Breast Cancer · Node-positive Breast Cancer  ·  Sponsor: Kliniken Essen-Mitte

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Due to high pathological complete remission (pCR) rates in both breast and lymph nodes (ypT0/Tis, ypN0) following neoadjuvant systemic therapy (NST) in many patients with initially clinically node-positive (cN+) breast cancer, the standard treatment of the axilla has changed from axillary lymph node dissection (ALND), which is associated with high morbidity, to less invasive, surgical approaches. In several studies, targeted axillary dissection (TAD) has presented with false-negative rates (FNRs) less than 5%, however, in patients with high initial lymph node involvement (≥ 3 clinically suspicious lymph nodes) TAD has not been thoroughly investigated. The present prospective registry study aims to evaluate the FNR of TAD in patients with ≥ 3 initially suspicious lymph nodes and clinically node-negative status (ycN0) after NST in comparison to ALND.

This description comes directly from the study's public registry record.

Talk to the study team

Oliver Halfmann  ·  +49201174  ·  O.Halfmann@kem-med.com

Dorothea Schindowski  ·  +49201174  ·  D.Schindowski@kem-med.com

Always discuss trial participation with your own doctor first.

Locations (1)

Kliniken Essen-Mitte (KEM)Essen, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT05462457