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      Second International Consensus Conference on lesions of uncertain malignant potential in the breast (B3 lesions)

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          Abstract

          Purpose

          The second International Consensus Conference on B3 lesions was held in Zurich, Switzerland, in March 2018, organized by the International Breast Ultrasound School to re-evaluate the consensus recommendations.

          Methods

          This study (1) evaluated how management recommendations of the first Zurich Consensus Conference of 2016 on B3 lesions had influenced daily practice and (2) reviewed current literature towards recommendations to biopsy.

          Results

          In 2018, the consensus recommendations for management of B3 lesions remained almost unchanged: For flat epithelial atypia (FEA), classical lobular neoplasia (LN), papillary lesions (PL) and radial scars (RS) diagnosed on core-needle biopsy (CNB) or vacuum-assisted biopsy (VAB), excision by VAB in preference to open surgery, and for atypical ductal hyperplasia (ADH) and phyllodes tumors (PT) diagnosed at VAB or CNB, first-line open surgical excision (OE) with follow-up surveillance imaging for 5 years. Analyzing the Database of the Swiss Minimally Invasive Breast Biopsies (MIBB) with more than 30,000 procedures recorded, there was a significant increase in recommending more frequent surveillance of LN [65% in 2018 vs. 51% in 2016 ( p = 0.004)], FEA (72% in 2018 vs. 62% in 2016 ( p = 0.005)), and PL [(76% in 2018 vs. 70% in 2016 ( p = 0.04)] diagnosed on VAB. A trend to more frequent surveillance was also noted also for RS [77% in 2018 vs. 67% in 2016 ( p = 0.07)].

          Conclusions

          Minimally invasive management of B3 lesions (except ADH and PT) with VAB continues to be appropriate as an alternative to first-line OE in most cases, but with more frequent surveillance, especially for LN.

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          Most cited references87

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          European guidelines for quality assurance in breast cancer screening and diagnosis. Fourth edition--summary document.

          Breast cancer is a major cause of suffering and death and is of significant concern to many women. Early detection of breast cancer by systematic mammography screening can find lesions for which treatment is more effective and generally more favourable for quality of life. The potential harm caused by mammography includes the creation of unnecessary anxiety and morbidity, inappropriate economic cost and the use of ionising radiation. It is for this reason that the strongest possible emphasis on quality control and quality assurance is required. Development of the European Guidelines for Quality Assurance in Breast Cancer Screening and Diagnosis has been an initiative within the Europe Against Cancer Programme. The fourth edition of the multidisciplinary guidelines was published in 2006 and comprises approximately 400 pages divided into 12 chapters prepared by >200 authors and contributors. The multidisciplinary editorial board has prepared a summary document to provide an overview of the fundamental points and principles that should support any quality screening or diagnostic service. This document includes a summary table of key performance indicators and is presented here in order to make these principles and standards known to a wider scientific community.
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            Adhesion molecule signalling: not always a sticky business.

            The signalling activity of cell adhesion molecules (CAMs) such as cadherins, immunoglobulin-like CAMs or integrins has long been considered to be a direct consequence of their adhesive properties. However, there are physiological and pathological processes that reduce or even abrogate the adhesive properties of CAMs, such as cleavage, conformational changes, mutations and shedding. In some cases these 'adhesion deficient' CAMs still retain signalling properties through their cytoplasmic domains and/or their mutated or truncated extracellular domains. The ability of CAMs to activate signal transduction cascades in the absence of cell adhesion significantly extends their range of biological activities.
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              Bilateral risk for subsequent breast cancer after lobular carcinoma-in-situ: analysis of surveillance, epidemiology, and end results data.

              Noninvasive lesions involving the lobules of the breast are increasingly diagnosed as incidental microscopic findings at the time of lumpectomy or core-needle biopsy. We investigated the incidence rates of invasive breast cancer (IBC) after a diagnosis of lobular carcinoma-in-situ (LCIS) by using Surveillance, Epidemiology, and End Results (SEER) data. Patients (N = 4,853) having a diagnosis of primary LCIS in the time period of 1973 to 1998 were identified using the SEER Public Use CD-ROM data. The database was then searched for patients with subsequent primary IBC occurrences (n = 350). The clinical and pathologic characteristics of patients with subsequent primary IBCs were compared with the characteristics of patients with primary IBCs attained during the same time period (N = 255,114). The incidence of IBC increased over time from diagnosis of LCIS, with 7.1% +/- 0.5% incidence of IBC at 10 years. IBCs detected after partial mastectomy occurred in either breast (46% ipsilateral and 54% contralateral); however, after mastectomy, most IBCs were contralateral (94.7%). IBCs occurring after LCIS more often represented invasive lobular histology (23.1%) compared with primary IBCs (6.5%). The standardized incidence ratio (the ratio of observed to expected cases) for developing IBC was 2.4 (95% CI, 2.1 to 2.6) adjusted for age and year of diagnosis. LCIS is associated with increased risk of subsequent invasive disease, with equal predisposition in either breast. The minimum risk of developing IBC after LCIS is 7.1% at 10 years.
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                Author and article information

                Contributors
                +41 79 642 67 52 , jcr@2cr.ch
                Journal
                Breast Cancer Res Treat
                Breast Cancer Res. Treat
                Breast Cancer Research and Treatment
                Springer US (New York )
                0167-6806
                1573-7217
                30 November 2018
                30 November 2018
                2019
                : 174
                : 2
                : 279-296
                Affiliations
                [1 ]ISNI 0000 0001 0721 9812, GRID grid.150338.c, Département de Gynécologie et d’Obstétrique, Centre du sein, , Hôpitaux Universitaires de Genève, ; Bd de la Cluse 30, 1211 Geneva 14, Switzerland
                [2 ]GRID grid.451349.e, The Rose Centre, , St George’s University Hospitals NHS Foundation Trust, ; Perimeter Road, London, SW17 0QT UK
                [3 ]ISNI 0000 0001 2171 9952, GRID grid.51462.34, Breast Imaging Service, Department of Radiology, , Memorial Sloan Kettering Cancer Center, ; 300 E 66th St, New York, NY 10065 USA
                [4 ]ISNI 0000 0004 0508 7512, GRID grid.482962.3, Department of Medical Services, Institute of Radiology, , Kantonsspital Baden, ; im Ergel, 5404 Baden, Switzerland
                [5 ]ISNI 0000 0004 0479 2981, GRID grid.490240.b, Zentrum Radiologie der Niels-Stensen-Kliniken; Marienhospital Osnabrück, ; Bischofsstraße 1, 49074 Osnabrück, Germany
                [6 ]ISNI 0000 0001 0211 9062, GRID grid.491786.5, Institut für Pathologie am Dietrich-Bonhoeffer-Klinikum, ; Salvador-Allende-Straße 30, 17036 Neubrandenburg, Germany
                [7 ]Brust-Zentrum Zürich, Seefeldstr. 214, 8008 Zurich, Switzerland
                [8 ]ISNI 0000 0004 0479 0855, GRID grid.411656.1, Interventional and Pediatric Radiology, Department of Diagnostic, , Inselspital, University Hospital Bern, ; Freiburgstrasse 10, 3010 Bern, Switzerland
                [9 ]ISNI 0000 0000 9259 8492, GRID grid.22937.3d, Department of Biomedical Imaging and Image-guided Therapy, Allgemeines Krankenhaus, , Medical University of Vienna, ; Währinger Gürtel 18-20, 1090 Vienna, Austria
                [10 ]ISNI 0000 0004 1936 973X, GRID grid.5252.0, Department of Radiology, University Hospital, , Ludwig Maximilian University Munich, ; Marchioninistr. 15, 81377 Munich, Germany
                [11 ]ISNI 0000 0004 1757 1758, GRID grid.6292.f, Department of Biomedical and Neuromotor Sciences, Unit of Anatomic Pathology at Bellaria Hospital, , University of Bologna, ; Via Altura 3, 40139 Bologna, Italy
                [12 ]ISNI 0000 0004 1937 0642, GRID grid.6612.3, Clinic of Radiology and Nuclear Medicine, University Hospital Basel, , University of Basel, ; Petersgraben 4, 4031 Basel, Switzerland
                [13 ]ISNI 0000 0001 2294 4705, GRID grid.413349.8, Breast Center St. Gallen, , Cantonal Hospital St. Gallen, ; Rorschacher Str. 95, 9007 St. Gallen, Switzerland
                [14 ]ISNI 0000 0004 1784 3645, GRID grid.440907.e, Imaging Department, Institut Curie, , PSL Research University, ; Paris, France
                [15 ]Division of Radiology, Breast Center Bern (Brustzentrum Bern), Klinik Engeried, Lindenhofgruppe AG, Riedweg 15, 3012 Bern, Switzerland
                [16 ]ISNI 0000 0004 0478 9977, GRID grid.412004.3, Institute of Diagnostic and Interventional Radiology, , University Hospital Zurich, ; Rämistr. 100, 8091 Zurich, Switzerland
                [17 ]ISNI 0000 0004 0478 9977, GRID grid.412004.3, Institute of Pathology and Molecular Pathology, , University Hospital Zurich, ; Switzerland Schmelzbergstrasse 12., 8091 Zurich, Switzerland
                [18 ]Ringlikerstrasse 53, 8142 Uitikon Waldegg, Switzerland
                Author information
                http://orcid.org/0000-0001-9117-2825
                Article
                5071
                10.1007/s10549-018-05071-1
                6538569
                30506111
                d84c67f1-1f3f-42da-8256-0f9f1c63d8db
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 21 November 2018
                : 23 November 2018
                Categories
                Review
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2019

                Oncology & Radiotherapy
                b3 lesions,vacuum-assisted biopsy,consensus,breast,uncertain malignant potential,breast surgery

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