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      Epidemiological characteristics, clinical outcomes and management patterns of metastatic breast cancer patients in routine clinical care settings of Greece: Results from the EMERGE multicenter retrospective chart review study

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          Abstract

          Background

          The “EMERGE” study, aimed to capture real-life management patterns and outcomes in metastatic breast cancer (MBC) in Greece, also accounting for hormone (HR) and human epidermal growth factor receptor 2 (HER2) status.

          Methods

          “EMERGE” was a multicenter, retrospective cohort study of adult MBC patients diagnosed between 01-Janaury-2010 and 30-June-2012, either de novo or having progressed from a non-metastatic state. Patient data, including treatment patterns and outcomes, were mainly abstracted through medical chart review.

          Results

          386 patients were enrolled by 16 hospital-based oncologists between 12-March-2013 and 31-March-2015. The median look-back period was 29.1 months. At MBC diagnosis, 56.1% of the patients were HR +/HER2 , 16.6% HR +/HER2 +, 14.5% HR /HER2 , and 12.8% HR /HER2 +. In the first line setting, chemotherapy, targeted therapy and endocrine therapy were received by 76.7, 52.4, and 28.3% of the overall population, and by 66.5/36.2/42.0%, 80.4/80.4/28.6%, 88.4/90.7/0.0, and 95.6%/56.5/6.5% of the HR +/HER2 , HR +/HER2 +, HR /HER2 +, HR /HER2 subpopulations, respectively. In the overall population, the disease progression incidence rate was 0.57 [95% confidence interval (CI): 0.48–0.67] per person-year; median progression-free survival (PFS) was 22.4 (95% CI: 20.4–24.7) and overall survival (OS) was 45.0 (95% CI: 40.9–55.0) months. Median PFS was 24.6 (95% CI: 21.3–27.9) in HR +/HER2 , 19.7 (95% CI: 12.9–25.9) in HR +/HER2 +, 23.0 (95% CI: 16.6–29.7) in HR /HER2 + and 18.3 (95% CI: 10.0–24.7) months in HR /HER2 subpopulations. A multivariable Cox proportional hazards model, adjusted among other factors for age and duration of diagnosis, HR and HER2 status, demonstrated that in the overall population PFS was better among those receiving first line endocrine therapy (hazard ratio: 0.70; 95%CI: 0.51–0.95; p = 0.024).

          Conclusions

          “EMERGE” demonstrates differences between HR/HER2 subtypes in clinical outcomes and divergence from evidence-based guideline recommendations for MBC management, especially as it pertains to the HR +/HER2 patients in which chemotherapy was favored over endocrine therapy in the first line setting.

          Study registration

          The study has been registered on the electronic Registry of Non-Interventional Studies (RNIS) posted on the website of the Hellenic Association of Pharmaceutical Companies (SFEE): https://www.dilon.sfee.gr/studiesp_d.php?meleti_id=NIS-OGR-XXX-2012/1

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          Most cited references18

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          Biology and Management of Patients With Triple-Negative Breast Cancer.

          : Triple-negative breast cancer (TNBC) accounts for 15% of all breast cancers and is associated with poor long-term outcomes compared with other breast cancer subtypes. Because of the lack of approved targeted therapy, at present chemotherapy remains the mainstay of treatment for early and advanced disease. TNBC is enriched for germline BRCA mutation, providing a foundation for the use of this as a biomarker to identify patients suitable for treatment with DNA-damaging agents. Inherited and acquired defects in homologous recombination DNA repair, a phenotype termed "BRCAness," may be present in a large proportion of TNBC cases, making it an attractive selection and response biomarker for DNA-damaging therapy. Triple-negative breast cancer is a diverse entity for which additional subclassifications are needed. Increasing understanding of biologic heterogeneity of TNBC has provided insight into identifying potentially effective systemic therapies, including cytotoxic and targeted agents. Numerous experimental approaches are under way, and several encouraging drug classes, such as immune checkpoint inhibitors, poly(ADP-ribose) polymerase inhibitors, platinum agents, phosphatidylinositol-3-kinase pathway inhibitors, and androgen receptor inhibitors, are being investigated in TNBC. Molecular biomarker-based patient selection in early-phase trials has the potential to accelerate development of effective therapies for this aggressive breast cancer subtype. TNBC is a complex disease, and it is likely that several different targeted approaches will be needed to make meaningful strides in improving the outcomes.
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            Breast cancer metastasis: challenges and opportunities.

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              Incidence and patterns of distant metastases for patients with early-stage breast cancer after breast conservation treatment.

              Breast conservation treatment (BCT), consisting of breast conservation surgery followed by definitive radiation therapy (RT), has been shown to be effective for early-stage breast cancer. Patterns of metastatic failure by specific anatomic site are not well described in the literature. A total of 1754 patients with stage I or II invasive carcinoma of the breast treated with BCT between 1977 and 2003 were identified. Patients were scored based on first site of metastasis: bone, brain, lung, liver, or other. Non-breast cancer deaths, contralateral breast cancer, and second malignancies were treated as competing risks events. Cumulative incidence functions for each competing event were calculated using competing risk methodology. Univariate analysis was performed to determine the hazard ratio (HR) associated with patient and tumor characteristics. The most common event was non-breast cancer death (16.5% at 15 years; 95% confidence interval [CI], 13.9%-19.4%). The most common exclusive first site of metastasis was bone (5.9% at 15 years). The 4 most common anatomic sites of distant metastases as the first exclusive event were bone (41.1%), lung (22.4%), liver (7.3%), and brain (7.3%). The present study has demonstrated the site-specific risks of metastases. These data support current clinical practice of screening for site-specific metastatic disease after BCT based on concerning patient-specific signs or symptoms. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                kotsakis@med.uoc.gr
                ardavanis@yahoo.com
                gkoumak@otenet.gr
                epsam@otenet.gr
                psyrri237@yahoo.com
                +30 210 7286305 , +30 697 4441501 , chr_papadim@yahoo.gr
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                18 January 2019
                18 January 2019
                2019
                : 19
                : 88
                Affiliations
                [1 ]GRID grid.412481.a, Department of Medical Oncology, , University General Hospital of Heraklion Crete Voutes, ; 711 10, Iraklio, Greece
                [2 ]1st Department of Medical Oncology, Agios Savvas Anticancer Hospital, 171 Alexandras Av, 115 22 Athens, Greece
                [3 ]2nd Department of Medical Oncology, Agios Savvas Anticancer Hospital, 171 Alexandras Av, 115 22 Athens, Greece
                [4 ]GRID grid.470050.6, 3rd Department of Medical Oncology, , Agii Anargiri Cancer Hospital, ; Kaliftaki 145, 14564 N. Kifissia, Athens, Greece
                [5 ]ISNI 0000 0004 0622 4662, GRID grid.411449.d, Medical Oncology Unit, , ATTIKON University Hospital, ; 1 Rimini St, 124 62 Athens, Greece
                [6 ]GRID grid.413862.a, Oncology Unit, 2nd Department of Surgery, , Aretaieion Hospital, ; 76 Vas. Sofias Av, 115 28 Athens, Greece
                Author information
                http://orcid.org/0000-0001-8084-0445
                Article
                5301
                10.1186/s12885-019-5301-5
                6339387
                30658600
                c08e81fb-47d0-4aab-b7e5-3a62371b7117
                © The Author(s). 2019

                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. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 December 2017
                : 10 January 2019
                Funding
                Funded by: AstraZeneca Greece(GR)
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Oncology & Radiotherapy
                metastatic breast cancer,hormone receptor,human epidermal growth factor receptor 2,treatment patterns,progression-free survival,overall survival,greece

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