Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT04854005

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

Selective Use of ALND in N1 HR+/HER2- Breast Cancer Patients With 1 or 2 Positive Sentinel Lymph Nodes Undergoing Upfront Breast Surgery and Adjuvant Radiation: A Prospective Study

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
78 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREBreast surgeryPatients will undergo SLNB with single or dual-tracer lymphatic with technetium-99m sulfur colloid either lymphazurin or methylene blue dye, per institution standard, in accordance with routine clinical practice.

Timeline

Start date
2021-04-20
Primary completion
2026-04-01
Completion
2026-04-01
First posted
2021-04-22
Last updated
2026-01-12

Locations

10 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT04854005. Inclusion in this directory is not an endorsement.