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Study identifier: NCT04854005 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Active Not Recruiting

Use of Sentinel Lymph Node Biopsy in Patients With Early-Stage, Palpable Node-Positive HR+/HER2- Breast Cancer Having Upfront Surgery and Adjuvant Radiation

Condition: Breast Cancer  ·  Sponsor: Memorial Sloan Kettering Cancer Center

PhaseN/A
Planned participants78
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to find out how often the researchers can avoid an ALND in patients with early-stage, node-positive HR+/HER2- breast cancer who are having upfront surgery. The study researchers think that, if AUS before surgery can help identify people who may have up to 3 affected lymph nodes, it will be possible to perform the less radical standard SLNB during surgery.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (10)

Hartford Healthcare Cancer Alliance (Data collection only)Hartford, Connecticut, United States
University of Michigan (Data Collection Only)Ann Arbor, Michigan, United States
Memorial Sloan Kettering Basking Ridge (Consent Only)Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Monmouth (All Protocol Activities)Middletown, New Jersey, United States
Memorial Sloan Kettering Bergen (Consent Only)Montvale, New Jersey, United States
Memorial Sloan Kettering Suffolk - Commack (Consent Only)Commack, New York, United States
Memorial Sloan Kettering Westchester (Consent Only)Harrison, New York, United States
Memorial Sloan Kettering Cancer CenterNew York, New York, United States
Memorial Sloan Kettering Nassau (Consent Only)Uniondale, New York, United States
Lehigh Valley Health Network (Dara Collection Only)Allentown, Pennsylvania, United States

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