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Targeted Axillary Dissection After Neo-adjuvant Chemotherapy

Feasability Study of a New Technique of Axillary Evaluation in Patients With Node Positive Breast Cancer Following Neo-adjuvant Chemotherapy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05071911
Enrollment
100
Registered
2021-10-08
Start date
2021-04-21
Completion date
2024-06-30
Last updated
2023-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

Currently most breast cancer patients with confirmed axillary lymph node metastasis (cN1) at diagnosis are candidates for neoadjuvant chemotherapy (NAC). The increased utilization of NAC can be attributed to practical clinical advantages. The increasing use of NAC has, however, introduced questions regarding appropriate loco-regional management, including the optimal surgical approach to the axillary lymph nodes. According to current guidelines, patients presenting with cN1 disease and treated with NAC, still undergo axillary lymph node dissection (ALND). In forty percent of these patients, however, the investigators see a nodal complete pathological response (ypN0). In certain subgroups, triple negative breast cancer and Her2 amplified breast cancer, this percentage is even higher. The investigators would like to lessen surgical morbidity by performing a targeted axillary dissection. The investigators place a clip in the biopsy-proven lymph node metastasis at diagnosis. After NAC, the investigators perform a dual agent sentinel node procedure and remove the clipped node during the same surgery. When these lymph nodes are microscopically tumor-free, the investigators can abolish an ALND. Targeted axillary dissection after NAC for cN1 disease seems to have acceptable false negative rates in previous trials. The investigators would like to further define patients where an ALND can be safely omitted.

Interventions

PROCEDURETAD (Targeted Axillary Dissection)

Dual agent SLNB + resection of proven lymph nodes metastasis marked with clip at diagnosis

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with cT1-3N1M0 breast cancer, histopathologically confirmed. * Age greater than or equal to 18 years and less than or equal to 85 years. * Necessity and agreement to neoadjuvant chemotherapy

Exclusion criteria

* Previous surgery ipsilateral axillary or radiation ipsilateral axillary / chest. * Extranodal metastases M1 * cN2-3 status * Breast cancer with direct invasion of chest wall and / or skin cT4 * Disease progression (clinical /radiological) under neoadjuvant treatment * Pregnancy * Presence of a pacemaker in the ipsilateral chest wall

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of new surgical technique TAD using Magseed90 minutesSuccesful retrievement of sentinel node and clipped node

Secondary

MeasureTime frame
Correlation between ITC/ micrometastasis / macrometastasis in retrieved TAD nodes and number of additional lymph node metastasis in ALNDTwo weeks

Countries

Belgium

Contacts

Primary ContactIne Luyten, MD
ine.luyten@uzbrussel.be+32 2 477 9398
Backup ContactBorstkliniek
borstkliniek@uzbrussel.be+32 2 477 6015

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026