Abstract
Purpose: Currently, various techniques are available to mark and selectively remove initially suspicious axillary lymph nodes (target lymph nodes, TLNs) in breast cancer patients receiving neoadjuvant chemotherapy (NACT). To date, limited data are available on whether the use of magnetic seeds (MS) is suitable for localizing TLNs. This study aimed to investigate the feasibility of MS in patients undergoing target lymph node biopsy (TLNB) or targeted axillary dissection (TAD) after NACT. Methods: Prospective data from the ongoing multicentric AXSANA study were extracted from selected patients in whom the TLN had been marked with an MS before NACT and who were enrolled from June 2020 to June 2023. The endpoints of the analysis were the detection rate, the rate of lost markers, and the potential impairment on magnetic resonance imaging (MRI) assessment. Results: In 187 patients from 27 study sites in seven countries, MS were placed into the TLN before NACT. In 151 of these, post-NACT surgery had been completed at the time of analysis. In 146 patients (96.0%), a TLN could successfully be detected. In three patients, the seed was removed but no lymphoid tissue was detected on histopathology. The rate of lost markers was 1.2% (2 out of 164 MS). In 15 out of 151 patients (9.9%), MRI assessment was reported to be compromised by MS placement. Conclusion: MS show excellent applicability for TLNB/TAD when inserted before NACT with a high DR and a low rate of lost markers. Axillary MS can impair MRI assessment of the breast. Trial registration number: NCT04373655 (date of registration May 4, 2020).
| Original language | English |
|---|---|
| Journal | Breast Cancer Research and Treatment |
| Volume | 202 |
| Issue number | 3 |
| Pages (from-to) | 497-504 |
| Number of pages | 8 |
| ISSN | 0167-6806 |
| DOIs | |
| Publication status | Published - 12.2023 |
Funding
Open Access funding enabled and organized by Projekt DEAL. This work was supported by the AGO Breast Study Group (AGO-B), the Claudia von Schilling Foundation for Breast Cancer Research, the Ehmann Foundation Savognin, Arbeitsgemeinschaft für ästhetische, plastische und wiederherstellende Operationsverfahren in der Gynäkologie e.V. (AWOgyn), EndoMag, Merit Medical GmbH, and Mammotome. The authors wish to thank Jana Shabbir, Bilge Sezen Aktas, Angelika Jursik, Markus Höing, and Marina Mangold for the coordination of the AXSANA study and all participating study sites for their valuable contribution to this trial. The AXSANA study is supported by the AGO‑B, the Claudia von Schilling Foundation for Breast Cancer Research, the Ehmann Foundation Savognin, AWOgyn, EndoMag, Merit Medical GmbH, Mammotome, German Breast Group Forschungs GmbH (GBG), and Nord-Ostdeutsche Gesellschaft für Gynäkologische Onkologie (NOGGO e.V.).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Areas and Centers
- Research Area: Luebeck Integrated Oncology Network (LION)
- Centers: University Cancer Center Schleswig-Holstein (UCCSH)
DFG Research Classification Scheme
- 2.22-14 Hematology, Oncology
- 2.22-21 Gynaecology and Obstetrics
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