Surgical Management of the Axilla in Clinically Node-Positive Breast Cancer Patients Converting to Clinical Node Negativity through Neoadjuvant Chemotherapy: Current Status, Knowledge Gaps, and Rationale for the EUBREAST-03 AXSANA Study
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
PubMed
33805367
PubMed Central
PMC8037995
DOI
10.3390/cancers13071565
PII: cancers13071565
Knihovny.cz E-zdroje
- Klíčová slova
- breast cancer, marked lymph node, neoadjuvant therapy, targeted axillary dissection, therapy response,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
In the last two decades, surgical methods for axillary staging in breast cancer patients have become less extensive, and full axillary lymph node dissection (ALND) is confined to selected patients. In initially node-positive patients undergoing neoadjuvant chemotherapy, however, the optimal management remains unclear. Current guidelines vary widely, endorsing different strategies. We performed a literature review on axillary staging strategies and their place in international recommendations. This overview defines knowledge gaps associated with specific procedures, summarizes currently ongoing clinical trials that address these unsolved issues, and provides the rationale for further research. While some guidelines have already implemented surgical de-escalation, replacing ALND with, e.g., sentinel lymph node biopsy (SLNB) or targeted axillary dissection (TAD) in cN+ patients converting to clinical node negativity, others recommend ALND. Numerous techniques are in use for tagging lymph node metastasis, but many questions regarding the marking technique, i.e., the optimal time for marker placement and the number of marked nodes, remain unanswered. The optimal number of SLNs to be excised also remains a matter of debate. Data on oncological safety and quality of life following different staging procedures are lacking. These results provide the rationale for the multinational prospective cohort study AXSANA initiated by EUBREAST, which started enrollment in June 2020 and aims at recruiting 3000 patients in 20 countries (NCT04373655; Funded by AGO-B, Claudia von Schilling Foundation for Breast Cancer Research, AWOgyn, EndoMag, Mammotome, and MeritMedical).
Brandenburg Medical School Theodor Fontane 16816 Neuruppin Germany
Breast Surgery Unit San Raffaele Hospital Milan 20132 Milano MI Italy
Breast Surgical Unit Clínica Universidad de Navarra 28027 Madrid Spain
Champalimaud Clinical Center Breast Unit Champalimaud Foundation 1400 038 Lisboa Portugal
Collegium Medicum University of Zielona Góra 65 046 Zielona Góra Poland
Department for Breast and Endocrine Surgery Oslo University Hospital 0188 Oslo Norway
Department of Breast and Sarcoma Surgery National Institute of Oncology 1122 Budapest Hungary
Department of Gynecology and Breast Cancer Center Charite Berlin 10117 Berlin Germany
Department of Gynecology and Obstetrics Klinikum Esslingen 73730 Esslingen Germany
Department of Gynecology and Obstetrics Regio Klinikum Pinneberg 25421 Pinneberg Germany
Department of Gynecology and Obstetrics University Hospital Aachen 52074 Aachen Germany
Department of Gynecology and Obstetrics University Hospital Rostock 18059 Rostock Germany
Department of Molecular Medicine and Surgery Karolinska Institutet 171 77 Stockholm Sweden
Department of Surgery Capio St Göran's Hospital 112 19 Stockholm Sweden
Faculty of Biomedicine University of the Italian Switzerland 6900 Lugano Switzerland
Institut für Pathologie Medical University of Graz 8010 Graz Austria
Medical Faculty Heinrich Heine University Düsseldorf 40225 Düsseldorf Germany
Oncology Hospital University Hospital Center Nene Tereza 1000 Tirana Albania
Petrov Research Institute of Oncology 197758 Saint Petersburg Russia
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Classe J.M., Loaec C., Gimbergues P., Alran S., de Lara C.T., Dupre P.F., Rouzier R., Faure C., Paillocher N., Chauvet M.P., et al. Sentinel lymph node biopsy without axillary lymphadenectomy after neoadjuvant chemotherapy is accurate and safe for selected patients: The GANEA 2 study. Breast Cancer Res. Treat. 2019;173:343–352. doi: 10.1007/s10549-018-5004-7. PubMed DOI
Hunt K.K., Yi M., Mittendorf E.A., Guerrero C., Babiera G.V., Bedrosian I., Hwang R.F., Kuerer H.M., Ross M.I., Meric-Bernstam F. Sentinel lymph node surgery after neoadjuvant chemotherapy is accurate and reduces the need for axillary dissection in breast cancer patients. Ann. Surg. 2009;250:558–566. doi: 10.1097/SLA.0b013e3181b8fd5e. PubMed DOI
Kahler-Ribeiro-Fontana S., Pagan E., Magnoni F., Vicini E., Morigi C., Corso G., Intra M., Canegallo F., Ratini S., Leonardi M.C., et al. Long-term standard sentinel node biopsy after neoadjuvant treatment in breast cancer: A single institution ten-year follow-up. Eur. J. Surg. Oncol. 2021;47:804–812. doi: 10.1016/j.ejso.2020.10.014. PubMed DOI
Kuehn T., Bauerfeind I., Fehm T., Fleige B., Hausschild M., Helms G., Lebeau A., Liedtke C., von Minckwitz G., Nekljudova V., et al. Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy (SENTINA): A prospective, multicentre cohort study. Lancet Oncol. 2013;14:609–618. doi: 10.1016/S1470-2045(13)70166-9. PubMed DOI
Boughey J.C., Suman V.J., Mittendorf E.A., Ahrendt G.M., Wilke L.G., Taback B., Leitch A.M., Kuerer H.M., Bowling M., Flippo-Morton T.S., et al. Sentinel lymph node surgery after neoadjuvant chemotherapy in patients with node-positive breast cancer: The ACOSOG Z1071 (Alliance) clinical trial. JAMA. 2013;310:1455–1461. doi: 10.1001/jama.2013.278932. PubMed DOI PMC
Chehade H.E.H., Headon H., El Tokhy O., Heeney J., Kasem A., Mokbel K. Is sentinel lymph node biopsy a viable alternative to complete axillary dissection following neoadjuvant chemotherapy in women with node-positive breast cancer at diagnosis? An updated meta-analysis involving 3,398 patients. Am. J. Surg. 2016;212:969–981. doi: 10.1016/j.amjsurg.2016.07.018. PubMed DOI
Boughey J.C., Ballman K.V., Le-Petross H.T., McCall L.M., Mittendorf E.A., Ahrendt G.M., Wilke L.G., Taback B., Feliberti E.C., Hunt K.K. Identification and Resection of Clipped Node Decreases the False-negative Rate of Sentinel Lymph Node Surgery in Patients Presenting With Node-positive Breast Cancer (T0-T4, N1-N2) Who Receive Neoadjuvant Chemotherapy: Results From ACOSOG Z1071 (Alliance) Ann. Surg. 2016;263:802–807. doi: 10.1097/SLA.0000000000001375. PubMed DOI PMC
Caudle A.S., Yang W.T., Krishnamurthy S., Mittendorf E.A., Black D.M., Gilcrease M.Z., Bedrosian I., Hobbs B.P., DeSnyder S.M., Hwang R.F., et al. Improved Axillary Evaluation Following Neoadjuvant Therapy for Patients With Node-Positive Breast Cancer Using Selective Evaluation of Clipped Nodes: Implementation of Targeted Axillary Dissection. J. Clin. Oncol. 2016;34:1072–1078. doi: 10.1200/JCO.2015.64.0094. PubMed DOI PMC
NCCN Clinical Practice Guidelines in Oncology, Breast Cancer, Version 1.2021—15 January 2021. NCCN.org. [(accessed on 27 March 2021)];2021 Available online: https://www.nccn.org/professionals/physician_gls/default.aspx#breast.
Cardoso F., Kyriakides S., Ohno S., Penault-Llorca F., Poortmans P., Rubio I.T., Zackrisson S., Senkus E., Committee E.G. Early breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2019;30:1674. doi: 10.1093/annonc/mdz189. PubMed DOI
Recommendations of the AGO Breast Committee: Diagnosis and Treatment of Patients with early and advanced Breast Cancer. [(accessed on 27 March 2021)]; Available online: www.ago-online.de.
Banys-Paluchowski M., Gruber I.V., Hartkopf A., Paluchowski P., Krawczyk N., Marx M., Brucker S., Hahn M. Axillary ultrasound for prediction of response to neoadjuvant therapy in the context of surgical strategies to axillary dissection in primary breast cancer: A systematic review of the current literature. Arch. Gynecol. Obstet. 2020;301:341–353. doi: 10.1007/s00404-019-05428-x. PubMed DOI
Consensus Guideline on the Management of the Axilla in Patients with Invasive/In-Situ Breast Cancer. The American Society of Breast Surgeons. [(accessed on 27 March 2021)];2019 Available online: https://www.breastsurgeons.org/docs/statements/Consensus-Guideline-on-the-Management-of-the-Axilla.pdf?v2.
Finnish Breast Cancer Group Rintasyöpäryhmän Valtakunnallinen Diagnostiikka—Ja Hoitosuositus. [(accessed on 1 December 2019)]; Available online: https://1587667.167.directo.fi/@Bin/c554c241df494d864925e07ad6aa705e/1614023914/application/pdf/186425/SRSR_Suositus_2019%20Joulukuu.pdf.
Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF): S3-Leitlinie Früherkennung, Diagnose, Therapie und Nachsorge des Mammakarzinoms, Version 4.3, AWMF Registernummer: 032-045OL. [(accessed on 10 June 2020)]; Available online: http://www.leitlinienprogramm-onkologie.de/leitlinien/mammakarzinom/
Lazar G., Kelemen P., Kosa C., Maraz R., Paszt A., Pavlovics G., Savolt A., Simonka Z., Toth D., Matrai Z. Modern surgical treatment of breast cancer. 4th Breast Cancer Consensus Conference. Magy Onkol. 2020;64:329–346. PubMed
Indian Council of Medical Research Consensus Document for Management of Breast Cancer. Department of Health Research MoHFW; New Delhi, India: 2016.
Recommendations of the Polish Society of Surgical Oncology (Surgical Treatment in Breast Neoplasms: Second Consensus) [(accessed on 27 March 2021)];2019 Available online: https://journals.viamedica.pl/oncology_in_clinical_practice/article/view/OCP.2017.0015/43197.
Ghid de Management al Cancerului Mamar. [(accessed on 1 December 2009)]; Available online: http://old.ms.ro/index.php?pag=181&pg=5.
Peltecu G., Median D., Vlad Ș., Tuinea L., Iancu G., Gică N., Nedelea F., Cigăran R., Chirculescu R., Lesaru M., et al. Cancerul Mamar. Societatea de Obstetrica si Ginecologie. [(accessed on 26 February 2021)]; Available online: https://sogr.ro/wp-content/uploads/2019/06/30.-Cancerul-mamar.pdf.
Bröstcancer-Nationellt Vårdprogram-SweBCG, 2020-02-11 Version: 3.0. [(accessed on 1 December 2020)]; Available online: http://www.swebcg.se/wp-content/uploads/2016/10/nationellt-vardprogram-brostcancer_200211.pdf.
Neoadjuverende Kemoterapi ved Brystkræft mhp . Danish Breast Cancer Group Guidelines. Danish Breast Cancer Group; Aarhus, Denmark: 2016. Down-Sizing og Down-Staging.
Associazione Italiana di Oncologia Medica (AIOM) Breast Neoplasms Guidelines. 2018 ed. Associazione Italiana di Oncologia Medica (AIOM); Milan, Italy: 2019.
IX Consenso Nacional de Cancro de Mama. Sociedade Portuguesa de Senologia; Coimbra, Portugal: 2017.
Clinical Guidelines Mammary Cancer. Прoфессиoнальные Aссoциации: Ассoциация oнкoлoгoв Рoссии Рoссийскoе oбществo клиническoй oнкoлoгии; Moscow, Russia: 2018.
De La Peña F.A., Andrés R., Garcia-Sáenz J.A., Manso L., Margelí M., Dalmau E., Pernas S., Prat A., Servitja S., Ciruelos E. SEOM clinical guidelines in early stage breast cancer (2018) Clin. Transl. Oncol. 2019;21:18–30. doi: 10.1007/s12094-018-1973-6. PubMed DOI PMC
Boileau J.F., Poirier B., Basik M., Holloway C.M., Gaboury L., Sideris L., Meterissian S., Arnaout A., Brackstone M., McCready D.R., et al. Sentinel node biopsy after neoadjuvant chemotherapy in biopsy-proven node-positive breast cancer: The SN FNAC study. J. Clin. Oncol. 2015;33:258–264. doi: 10.1200/JCO.2014.55.7827. PubMed DOI
Reinisch M., Heil J., Rüland A., Seiberling C., Harrach H., Schindowski D., Lubitz J., Ankel C., Grasshoff S.T., Deuschle P., et al. Prospective, multicenter registry trial to evaluate the clinical feasibility of targeted axillary dissection (TAD) in patients (pts) with breast cancer (BC) and core biopsy proven axillary involvement (cN+) Ann. Oncol. 2019;30:v56. doi: 10.1093/annonc/mdz240.003. DOI
Kuemmel S., Heil J., Rueland A., Seiberling C., Harrach H., Schindowski D., Lubitz J., Hellerhoff K., Ankel C., Grasshoff S.T., et al. A Prospective, Multicenter Registry Study to Evaluate the Clinical Feasibility of Targeted Axillary Dissection (TAD) in Node-Positive Breast Cancer Patients. Ann. Surg. 2020;4 doi: 10.1097/SLA.0000000000004572. PubMed DOI
Plecha D., Bai S., Patterson H., Thompson C., Shenk R. Improving the Accuracy of Axillary Lymph Node Surgery in Breast Cancer with Ultrasound-Guided Wire Localization of Biopsy Proven Metastatic Lymph Nodes. Ann. Surg. Oncol. 2015;22:4241–4246. doi: 10.1245/s10434-015-4527-y. PubMed DOI
Laws A., Dillon K., Kelly B.N., Kantor O., Hughes K.S., Gadd M.A., Smith B.L., Lamb L.R., Specht M. Node-Positive Patients Treated with Neoadjuvant Chemotherapy Can Be Spared Axillary Lymph Node Dissection with Wireless Non-Radioactive Localizers. Ann. Surg. Oncol. 2020;27:4819–4827. doi: 10.1245/s10434-020-08902-y. PubMed DOI
Nguyen T.T., Hieken T.J., Glazebrook K.N., Boughey J.C. Localizing the Clipped Node in Patients with Node-Positive Breast Cancer Treated with Neoadjuvant Chemotherapy: Early Learning Experience and Challenges. Ann. Surg. Oncol. 2017;24:3011–3016. doi: 10.1245/s10434-017-6023-z. PubMed DOI
Simons J.M., Scoggins M.E., Kuerer H.M., Krishnamurthy S., Yang W.T., Sahin A.A., Shen Y., Lin H., Bedrosian I., Mittendorf E.A., et al. Prospective Registry Trial Assessing the Use of Magnetic Seeds to Locate Clipped Nodes After Neoadjuvant Chemotherapy for Breast Cancer Patients. Ann. Surg. Oncol. 2021;8:1–7. doi: 10.1245/s10434-020-09542-y. PubMed DOI
Siso C., de Torres J., Esgueva-Colmenarejo A., Espinosa-Bravo M., Rus N., Cordoba O., Rodriguez R., Peg V., Rubio I.T. Intraoperative Ultrasound-Guided Excision of Axillary Clip in Patients with Node-Positive Breast Cancer Treated with Neoadjuvant Therapy (ILINA Trial): A New Tool to Guide the Excision of the Clipped Node After Neoadjuvant Treatment. Ann. Surg. Oncol. 2018;25:784–791. doi: 10.1245/s10434-017-6270-z. PubMed DOI
Sun J., Henry D.A., Carr M.J., Yazdankhahkenary A., Laronga C., Lee M.C., Hoover S.J., Sun W., Czerniecki B.J., Khakpour N., et al. Feasibility of Axillary Lymph Node Localization and Excision Using Radar Reflector Localization. Clin. Breast Cancer. 2020 doi: 10.1016/j.clbc.2020.08.001. In Press. PubMed DOI
Hartmann S., Reimer T., Gerber B., Stubert J., Stengel B., Stachs A. Wire localization of clip-marked axillary lymph nodes in breast cancer patients treated with primary systemic therapy. Eur. J. Surg. Oncol. 2018;44:1307–1311. doi: 10.1016/j.ejso.2018.05.035. PubMed DOI
Diego E.J., McAuliffe P.F., Soran A., McGuire K.P., Johnson R.R., Bonaventura M., Ahrendt G.M. Axillary Staging After Neoadjuvant Chemotherapy for Breast Cancer: A Pilot Study Combining Sentinel Lymph Node Biopsy with Radioactive Seed Localization of Pre-treatment Positive Axillary Lymph Nodes. Ann. Surg. Oncol. 2016;23:1549–1553. doi: 10.1245/s10434-015-5052-8. PubMed DOI
Martínez A.M., Roselló I.V., Gómez A.S., Catanese A., Molina M.P., Suarez M.S., Miguel I.P., Aulina L.B., Gozálvez C.R., Ibáñez J.F.J., et al. Advantages of preoperative localization and surgical resection of metastatic axillary lymph nodes using magnetic seeds after neoadjuvant chemotherapy in breast cancer. Surg. Oncol. 2021;36:28–33. doi: 10.1016/j.suronc.2020.11.013. PubMed DOI
Kim W.H., Kim H.J., Kim S.H., Jung J.H., Park H.Y., Lee J., Kim W.W., Park J.Y., Chae Y.S., Lee S.J. Ultrasound-guided dual-localization for axillary nodes before and after neoadjuvant chemotherapy with clip and activated charcoal in breast cancer patients: A feasibility study. BMC Cancer. 2019;19:859. doi: 10.1186/s12885-019-6095-1. PubMed DOI PMC
Balasubramanian R., Morgan C., Shaari E., Kovacs T., Pinder S.E., Hamed H., Sever A.R., Kothari A. Wire guided localisation for targeted axillary node dissection is accurate in axillary staging in node positive breast cancer following neoadjuvant chemotherapy. Eur. J. Surg. Oncol. 2020;46:1028–1033. doi: 10.1016/j.ejso.2019.12.007. PubMed DOI
Lim G.H., Teo S.Y., Gudi M., Ng R.P., Pang J., Tan Y.S., Lee Y.S., Allen J.C., Jr., Leong L.C.H. Initial results of a novel technique of clipped node localization in breast cancer patients postneoadjuvant chemotherapy: Skin Mark clipped Axillary nodes Removal Technique (SMART trial) Cancer Med. 2020;9:1978–1985. doi: 10.1002/cam4.2848. PubMed DOI PMC
Lim G.H., Gudi M., Teo S.Y., Ng R.P., Yan Z., Lee Y.S., Allen J.C., Jr., Leong L.C.H. Would Removal of All Ultrasound Abnormal Metastatic Lymph Nodes Without Sentinel Lymph Node Biopsy Be Accurate in Patients with Breast Cancer with Neoadjuvant Chemotherapy? Oncologist. 2020;25:e1621–e1627. doi: 10.1634/theoncologist.2020-0494. PubMed DOI PMC
Simons J., Nijnatten T.J.V., Koppert L.B., van der Pol C.C., Diest P.J.V., Jager A., Klaveren D.V., Kam B.L., Lobbes M.B., de Boer M., et al. Radioactive Iodine Seed placement in the Axilla with Sentinel lymph node biopsy after neoadjuvant chemotherapy in breast cancer: Results of the prospective multicenter RISAS trial. Gen. Sess. Abstr. 2021;81:GS1-10.
Donker M., Straver M.E., Wesseling J., Loo C.E., Schot M., Drukker C.A., van Tinteren H., Sonke G.S., Rutgers E.J., Peeters M.J.V. Marking axillary lymph nodes with radioactive iodine seeds for axillary staging after neoadjuvant systemic treatment in breast cancer patients: The MARI procedure. Ann. Surg. 2015;261:378–382. doi: 10.1097/SLA.0000000000000558. PubMed DOI
Thill M., Khandan F., Schnitzbauer T. Magseed®-basierte Langzeitmarkierung von Target Lymphknoten bei Patientinnen mit einem Mammakarzinom im Frühstadium unter neoadjuvanter Therapie—Erste Erfahrungen und Perspektiven. GebFra. 2020;80 doi: 10.1055/s-010-49508. DOI
Malter W., Eichler C., Hanstein B., Mallmann P., Holtschmidt J. First Reported Use of Radiofrequency Identification (RFID) Technique for Targeted Excision of Suspicious Axillary Lymph Nodes in Early Stage Breast Cancer—Evaluation of Feasibility and Review of Current Recommendations. Vivo. 2020;34:1207–1213. doi: 10.21873/invivo.11894. PubMed DOI PMC
Hartmann S., Stachs A., Kühn T., Winckelmann A., De Boniface J., Gerber B., Reimer T. Target Lymph Node Biopsy (TLNB) nach Kohlenstoffmarkierung bei Mammakarzinom-Patientinnen im Rahmen der primären Systemtherapie—Ergebnisse der TATTOO-Studie (DGGG-Kongress) GebFra. 2020;80:61. doi: 10.1055/s-010-49508. DOI
Natsiopoulos I., Intzes S., Liappis T., Zarampoukas K., Zarampoukas T., Zacharopoulou V., Papazisis K. Axillary Lymph Node Tattooing and Targeted Axillary Dissection in Breast Cancer Patients Who Presented as cN+ Before Neoadjuvant Chemotherapy and Became cN0 After Treatment. Clin. Breast Cancer. 2019;19:208–215. doi: 10.1016/j.clbc.2019.01.013. PubMed DOI
Allweis T.M., Menes T., Rotbart N., Rapson Y., Cernik H., Bokov I., Diment J., Magen A., Golan O., Levi-Bendet N., et al. Ultrasound guided tattooing of axillary lymph nodes in breast cancer patients prior to neoadjuvant therapy, and identification of tattooed nodes at the time of surgery. Eur. J. Surg. Oncol. 2020;46:1041–1045. doi: 10.1016/j.ejso.2019.11.501. PubMed DOI
Khallaf E., Wessam R., Abdoon M. Targeted axillary dissection of carbon-tattooed metastatic lymph nodes in combination with post-neo-adjuvant sentinel lymph node biopsy using 1% methylene blue in breast cancer patients. Breast J. 2020;26:1061–1063. doi: 10.1111/tbj.13736. PubMed DOI
Gatek J., Petru V., Kosac P., Ratajsky M., Duben J., Dudesek B., Jancik P., Zabojnikova M., Katrusak J., Opelova P., et al. Targeted axillary dissection with preoperative tattooing of biopsied positive axillary lymph nodes in breast cancer. Neoplasma. 2020;67:1329–1334. doi: 10.4149/neo_2020_191228N1344. PubMed DOI
Choy N., Lipson J., Porter C., Ozawa M., Kieryn A., Pal S., Kao J., Trinh L., Wheeler A., Ikeda D., et al. Initial results with preoperative tattooing of biopsied axillary lymph nodes and correlation to sentinel lymph nodes in breast cancer patients. Ann. Surg. Oncol. 2015;22:377–382. doi: 10.1245/s10434-014-4034-6. PubMed DOI
Van Nijnatten T.J.A., Simons J.M., Smidt M.L., van der Pol C.C., van Diest P.J., Jager A., van Klaveren D., Kam B.L.R., Lobbes M.B.I., de Boer M., et al. A Novel Less-invasive Approach for Axillary Staging after Neoadjuvant Chemotherapy in Patients with Axillary Node-positive Breast Cancer by Combining Radioactive Iodine Seed Localization in the Axilla with the Sentinel Node Procedure (RISAS): A Dutch Prospective Multicenter Validation Study. Clin. Breast Cancer. 2017;17:399–402. doi: 10.1016/j.clbc.2017.04.006. PubMed DOI
Gera R., Tayeh S., Al-Reefy S., Mokbel K. Evolving Role of Magseed in Wireless Localization of Breast Lesions: Systematic Review and Pooled Analysis of 1,559 Procedures. Anticancer Res. 2020;40:1809–1815. doi: 10.21873/anticanres.14135. PubMed DOI
Kasem I., Mokbel K. Savi Scout(R) Radar Localisation of Non-palpable Breast Lesions: Systematic Review and Pooled Analysis of 842 Cases. Anticancer Res. 2020;40:3633–3643. doi: 10.21873/anticanres.14352. PubMed DOI
Lowes S., Bell A., Milligan R., Amonkar S., Leaver A. Use of Hologic LOCalizer radiofrequency identification (RFID) tags to localise impalpable breast lesions and axillary nodes: Experience of the first 150 cases in a UK breast unit. Clin. Radiol. 2020;75:942–949. doi: 10.1016/j.crad.2020.08.014. PubMed DOI
McGugin C., Spivey T., Coopey S., Smith B., Kelly B., Gadd M., Hughes K., Dontchos B., Specht M. Radiofrequency identification tag localization is comparable to wire localization for non-palpable breast lesions. Breast Cancer Res. Treat. 2019;177:735–739. doi: 10.1007/s10549-019-05355-0. PubMed DOI
Glaeser A., Sinn H.P., Garcia-Etienne C., Riedel F., Hug S., Schaefgen B., Golatta M., Hennigs A., Feisst M., Sohn C., et al. Heterogeneous Responses of Axillary Lymph Node Metastases to Neoadjuvant Chemotherapy are Common and Depend on Breast Cancer Subtype. Ann. Surg. Oncol. 2019;26:4381–4389. doi: 10.1245/s10434-019-07915-6. PubMed DOI
United State Nuclear Regulatory Commission Low Activity Radioactive Seeds Used for Localization of Non-Palpable Lesions and Lymph Nodes, Licensing Guidance, Revision 1. [(accessed on 1 December 2016)]; Available online: https://www.nrc.gov/docs/ML1619/ML16197A568.pdf.
Kirkilesis G., Constantinidou A., Kontos M. False negativity of targeted axillary dissection in breast cancer. Breast Care. 2021 doi: 10.1159/000513037. In Press. PubMed DOI PMC
Kantor O., Sipsy L.M., Yao K., James T.A. A Predictive Model for Axillary Node Pathologic Complete Response after Neoadjuvant Chemotherapy for Breast Cancer. Ann. Surg. Oncol. 2018;25:1304–1311. doi: 10.1245/s10434-018-6345-5. PubMed DOI
Tadros A.B., Yang W.T., Krishnamurthy S., Rauch G.M., Smith B.D., Valero V., Black D.M., Lucci A., Jr., Caudle A.S., DeSnyder S.M., et al. Identification of Patients With Documented Pathologic Complete Response in the Breast After Neoadjuvant Chemotherapy for Omission of Axillary Surgery. JAMA Surg. 2017;152:665–670. doi: 10.1001/jamasurg.2017.0562. PubMed DOI PMC
Barron A.U., Hoskin T.L., Day C.N., Hwang E.S., Kuerer H.M., Boughey J.C. Association of Low Nodal Positivity Rate Among Patients With ERBB2-Positive or Triple-Negative Breast Cancer and Breast Pathologic Complete Response to Neoadjuvant Chemotherapy. JAMA Surg. 2018;153:1120–1126. doi: 10.1001/jamasurg.2018.2696. PubMed DOI PMC
Esgueva A., Siso C., Espinosa-Bravo M., Sobrido C., Miranda I., Salazar J.P., Rubio I.T. Leveraging the increased rates of pathologic complete response after neoadjuvant treatment in breast cancer to de-escalate surgical treatments. J. Surg. Oncol. 2021;123:71–79. doi: 10.1002/jso.26236. PubMed DOI
Koolen B.B., Donker M., Straver M.E., van der Noordaa M.E.M., Rutgers E.J.T., Olmos R.A.V., Peeters M.V. Combined PET-CT and axillary lymph node marking with radioactive iodine seeds (MARI procedure) for tailored axillary treatment in node-positive breast cancer after neoadjuvant therapy. Br. J. Surg. 2017;104:1188–1196. doi: 10.1002/bjs.10555. PubMed DOI
Hartmann S., Stachs A., Kühn T., Winckelmann A., de Boniface J., Gerber B., Reimer T. Abstract OT3-01-01: Feasibility of carbon tattooing for targeted lymph node biopsy in breast cancer patients treated by primary systemic therapy (TATTOO trial) Cancer Res. 2019;80:OT3-01. doi: 10.1158/1538-7445.SABCS19-OT3-01-01. DOI
Henke G., Knauer M., Ribi K., Hayoz S., Gerard M.A., Ruhstaller T., Zwahlen D.R., Muenst S., Ackerknecht M., Hawle H., et al. Tailored axillary surgery with or without axillary lymph node dissection followed by radiotherapy in patients with clinically node-positive breast cancer (TAXIS): Study protocol for a multicenter, randomized phase-III trial. Trials. 2018;19:667. doi: 10.1186/s13063-018-3021-9. PubMed DOI PMC