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      Cutaneous T-cell lymphoma with CNS involvement: a case series and review of the literature

      case-report

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          Abstract

          Cutaneous T-cell lymphoma (CTCL) is a rare hematologic malignancy that traditionally presents with cutaneous lesions, though metastases are not uncommon in progressive disease. We describe four cases of CTCL with central nervous system (CNS) involvement, detailing the history, pathological characteristics, treatment response, and progression. Median time from initial diagnosis to CNS metastasis was ∼5.4 years (range 3.4–15.5 years) and survival after metastasis was ∼160 days (range 19 days–4.4 years). No patients achieved long-term (>5 years) survival, though some displayed varying degrees of remission following CNS-directed therapy. We conclude that clinicians must be attentive to the development of CNS metastases in patients with CTCL. The growing body of literature on such cases will inform evolving therapeutic guidelines on this rare CTCL complication.

          Plain language summary

          Cutaneous T-cell lymphoma (CTCL) is a rare cancer of the blood, which typically manifests with skin lesions, such as itchy, scaly rashes that may thicken to form tumors on the skin. Though uncommon, metastases do occur in CTCL. A particularly rare location for these metastases is the central nervous system. This case series recounts the story of four unique patients and the presentation, diagnosis, and treatment of their CTCL, which unfortunately progressed to involve the central nervous system. Outcomes with central nervous system involvement in CTCL are poor, but may occur sometime later than a patient's initial diagnosis. Our patients had a median time from initial diagnosis to central nervous system metastases of ∼5.4 years and a survival of ∼160 days after central nervous system metastases. Some types of therapy, such as radiation, surgery, or chemotherapy, may be beneficial in extending survival or providing symptomatic relief for patients. It can be difficult to recognize symptoms of central nervous system metastases, so this case series emphasizes that vigilance for potential metastases and use of interdisciplinary teams is important in caring for these patients. This case series demonstrates the importance of continued research in this area, with the hope of improving outcomes for patients with central nervous system metastases of CTCL.

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          Most cited references44

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          Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

          Research electronic data capture (REDCap) is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: (1) a brief description of the REDCap metadata-driven software toolset; (2) detail concerning the capture and use of study-related metadata from scientific research teams; (3) measures of impact for REDCap; (4) details concerning a consortium network of domestic and international institutions collaborating on the project; and (5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions.
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            The REDCap consortium: Building an international community of software platform partners

            The Research Electronic Data Capture (REDCap) data management platform was developed in 2004 to address an institutional need at Vanderbilt University, then shared with a limited number of adopting sites beginning in 2006. Given bi-directional benefit in early sharing experiments, we created a broader consortium sharing and support model for any academic, non-profit, or government partner wishing to adopt the software. Our sharing framework and consortium-based support model have evolved over time along with the size of the consortium (currently more than 3200 REDCap partners across 128 countries). While the "REDCap Consortium" model represents only one example of how to build and disseminate a software platform, lessons learned from our approach may assist other research institutions seeking to build and disseminate innovative technologies.
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              Mogamulizumab versus vorinostat in previously treated cutaneous T-cell lymphoma (MAVORIC): an international, open-label, randomised, controlled phase 3 trial

              Cutaneous T-cell lymphomas are rare non-Hodgkin lymphomas with substantial morbidity and mortality in advanced disease stages. We compared the efficacy of mogamulizumab, a novel monoclonal antibody directed against C-C chemokine receptor 4, with vorinostat in patients with previously treated cutaneous T-cell lymphoma.
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                Author and article information

                Journal
                CNS Oncol
                CNS Oncol
                CNS
                CNS Oncology
                Future Medicine Ltd (London, UK )
                2045-0907
                2045-0915
                25 October 2023
                December 2023
                25 October 2023
                : 12
                : 4
                : CNS105
                Affiliations
                [1 ]Medical Scientist Training Program, Emory University School of Medicine, Atlanta, GA 30322, USA
                [2 ]Nutrition & Health Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322, USA
                [3 ]Emory University School of Medicine, Atlanta, GA 30322, USA
                [4 ]Division of Neuroradiology, Department of Radiology & Imaging Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA
                [5 ]Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA
                [6 ]Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA
                [7 ]Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA
                [8 ]Department of Hematology & Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA
                Author notes
                [* ]Author for correspondence: Tel.: +1 404 778 1900; pallen5@ 123456emory.edu
                Author information
                https://orcid.org/0000-0001-9834-3017
                https://orcid.org/0000-0001-9128-2004
                https://orcid.org/0009-0004-5893-4241
                https://orcid.org/0000-0002-1729-4629
                https://orcid.org/0000-0002-5644-9638
                https://orcid.org/0000-0002-3959-3662
                Article
                10.2217/cns-2023-0014
                10701703
                37877303
                1cd5a8cd-d469-43cb-bd5d-de5a7e694db3
                © 2023 Pamela Allen

                This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License

                History
                : 03 July 2023
                : 26 September 2023
                : 25 October 2023
                Page count
                Pages: 13
                Funding
                Funded by: Conquer Cancer Foundation;
                Award ID: 0000059354
                Funded by: National Cancer Institute;
                Award ID: F30CA243250, R01CA264519
                Funded by: Lymphoma Research Foundation;
                Award ID: 0000059101
                Funded by: National Institute of General Medical Sciences;
                Award ID: T32 GM008169
                Categories
                Case Series

                brain,metastasis,mycosis fungoides,sezary syndrome,visceral
                brain, metastasis, mycosis fungoides, sezary syndrome, visceral

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