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      Superparamagnetic Iron Oxide for Identifying Sentinel Lymph Node in Breast Cancer after Neoadjuvant Chemotherapy: Feasibility Study

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          Abstract

          Sentinel lymph node biopsy (SLNB) is a well-established procedure for staging clinically node-negative early breast cancer (BC). Superparamagnetic iron oxide (SPIO) demonstrated efficacy for nodal identification using a magnetic probe after local retroaeroal interstitial injection. Its benefits lie in its flexibility, which is an essential property in the global setting, where access to the isotope is difficult. To the best of our knowledge, this is the first study to evaluate the feasibility and safety of the SPIO for SLNB in BC patients treated with neoadjuvant chemotherapy (NAC). Seventy-four female patients were included. The median time of lymph node retrieval was 20 min. The median number of resected sentinel nodes (SNs) was 4. SN was detected in all patients. No serious adverse event was observed. SPIO in identifying SN in BC patients after NAC is feasible and oncologically safe.

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          Most cited references51

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          Early breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†

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            Breast Cancer, Version 3.2020, NCCN Clinical Practice Guidelines in Oncology

            Several new systemic therapy options have become available for patients with metastatic breast cancer, which have led to improvements in survival. In addition to patient and clinical factors, the treatment selection primarily depends on the tumor biology (hormone-receptor status and HER2-status). The NCCN Guidelines specific to the workup and treatment of patients with recurrent/stage IV breast cancer are discussed in this article.
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              Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial.

              Sentinel lymph node biopsy in women with operable breast cancer is routinely used in some countries for staging the axilla despite limited data from randomized trials on morbidity and mortality outcomes. We conducted a multicenter randomized trial to compare quality-of-life outcomes between patients with clinically node-negative invasive breast cancer who received sentinel lymph node biopsy and patients who received standard axillary treatment. The primary outcome measures were arm and shoulder morbidity and quality of life. From November 1999 to October 2003, 1031 patients were randomly assigned to undergo sentinel lymph node biopsy (n = 515) or standard axillary surgery (n = 516). Patients with sentinel lymph node metastases proceeded to delayed axillary clearance or received axillary radiotherapy (depending on the protocol at the treating institution). Intention-to-treat analyses of data at 1, 3, 6, and 12 months after surgery are presented. All statistical tests were two-sided. The relative risks of any lymphedema and sensory loss for the sentinel lymph node biopsy group compared with the standard axillary treatment group at 12 months were 0.37 (95% confidence interval [CI] = 0.23 to 0.60; absolute rates: 5% versus 13%) and 0.37 (95% CI = 0.27 to 0.50; absolute rates: 11% versus 31%), respectively. Drain usage, length of hospital stay, and time to resumption of normal day-to-day activities after surgery were statistically significantly lower in the sentinel lymph node biopsy group (all P .05). Sentinel lymph node biopsy is associated with reduced arm morbidity and better quality of life than standard axillary treatment and should be the treatment of choice for patients who have early-stage breast cancer with clinically negative nodes.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                16 July 2021
                July 2021
                : 10
                : 14
                : 3149
                Affiliations
                [1 ]Department of Surgical Oncology, Medical University of Lublin, Radziwiłłowska 13 St., 20-080 Lublin, Poland; andrzej.kurylcio@ 123456umlub.pl (A.K.); zuzanna.torun@ 123456gmail.com (Z.P.); magdalena.skorzewska@ 123456umlub.pl (M.S.); katarzyna.geca@ 123456umlub.pl (K.G.); sedlak.katarz@ 123456gmail.com (K.S.); p.kurylcio@ 123456gmail.com (P.K.); wojciech.polkowski@ 123456uml.edu.pl (W.P.)
                [2 ]Department of Human Physiology, Medical University of Lublin, Radziwiłłowska 11 St., 20-080 Lublin, Poland; radoslaw.mlak@ 123456uml.edu.pl (R.M.); teresa.malecka-massalska@ 123456umlub.pl (T.M.-M.)
                Author notes
                [* ]Correspondence: karolrawiczpruszynski@ 123456uml.edu.pl ; Tel.: +48-531-81-37
                Author information
                https://orcid.org/0000-0002-3312-9586
                https://orcid.org/0000-0003-3384-0324
                https://orcid.org/0000-0001-6455-5636
                Article
                jcm-10-03149
                10.3390/jcm10143149
                8305632
                34300315
                88ba295f-1a5c-4c76-96bd-a6b31c52681b
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 01 June 2021
                : 15 July 2021
                Categories
                Article

                breast cancer,neoadjuvant chemotherapy,sentinel lymph node,spio

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