RecruitingNCT05763641

TAD After Chemotherapy in Locally Advanced Breast Cancer

Target Axillary Dissection After Neoadjuvant Chemotherapy in Locally Advanced Breast Cancer


Sponsor

Hospital Universitari de Bellvitge

Enrollment

162 participants

Start Date

Feb 1, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

This is an observational study to validate target axillary dissection (TAD) in locally advanced tumors (cN2 and/or cT4).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying a surgical technique called TAD (targeted axillary dissection) in people with locally advanced breast cancer who have received pre-surgery chemotherapy. TAD aims to remove fewer lymph nodes than standard surgery while still accurately checking whether the cancer has responded to chemotherapy, reducing side effects like arm swelling (lymphedema). **You may be eligible if...** - Your breast cancer has spread to underarm lymph nodes (confirmed by biopsy) - You have at least 4 suspicious underarm lymph nodes, or a large tumor requiring underarm lymph node removal - You are receiving pre-surgery (neoadjuvant) chemotherapy **You may NOT be eligible if...** - Your cancer has spread very extensively to lymph nodes (cN3 stage) - Your breast cancer is the "luminal A" molecular subtype - You are receiving only hormone therapy (not chemotherapy) before surgery - You have cancer that has come back locally or spread to distant organs (metastatic) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURETarget Axillary Dissection

TAD after neoadjuvant chemotherapy and subsequent axillary lymph node dissection


Locations(2)

Hospital de Bellvitge

L'Hospitalet de Llobregat, Barcelona, Spain

Hospital Clínico y Provincial de Barcelona

Barcelona, Spain

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NCT05763641


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