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      Immune‐monitoring of myelodysplastic neoplasms: Recommendations from the i4MDS consortium

      research-article
      1 , 2 , 3 , 4 , 1 , 2 , 5 , 6 , 7 , 8 , 9 , 1 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 6 , 20 , 2 , 9 , 9 , 21 , 22 , 23 , 23 , 23 , 24 , 25 , 26 , 15 , 27 , 20 , 4 , 28 , 29 , 11 , 30 , 6 , 31 , 32 , 33 , 34 , 35 , 2 , 36 , 37 , 38 , 20 , 25 , 39 , 40 , 41 , 42 , 11 , 30 , 24 , 39 , 43 , 44 , 13 , 14 , 15 , 17 , 9 , 37 , 3 , 11 , , 1 , 45 , 6 , 2 , 16 , 34 , , i4MDS consortium
      HemaSphere
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          Abstract

          Advancements in comprehending myelodysplastic neoplasms (MDS) have unfolded significantly in recent years, elucidating a myriad of cellular and molecular underpinnings integral to disease progression. While molecular inclusions into prognostic models have substantively advanced risk stratification, recent revelations have emphasized the pivotal role of immune dysregulation within the bone marrow milieu during MDS evolution. Nonetheless, immunotherapy for MDS has not experienced breakthroughs seen in other malignancies, partly attributable to the absence of an immune classification that could stratify patients toward optimally targeted immunotherapeutic approaches. A pivotal obstacle to establishing “immune classes” among MDS patients is the absence of validated accepted immune panels suitable for routine application in clinical laboratories. In response, we formed International Integrative Innovative Immunology for MDS (i4MDS), a consortium of multidisciplinary experts, and created the following recommendations for standardized methodologies to monitor immune responses in MDS. A central goal of i4MDS is the development of an immune score that could be incorporated into current clinical risk stratification models. This position paper first consolidates current knowledge on MDS immunology. Subsequently, in collaboration with clinical and laboratory specialists, we introduce flow cytometry panels and cytokine assays, meticulously devised for clinical laboratories, aiming to monitor the immune status of MDS patients, evaluating both immune fitness and identifying potential immune “risk factors.” By amalgamating this immunological characterization data and molecular data, we aim to enhance patient stratification, identify predictive markers for treatment responsiveness, and accelerate the development of systems immunology tools and innovative immunotherapies.

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          Revised international prognostic scoring system for myelodysplastic syndromes.

          The International Prognostic Scoring System (IPSS) is an important standard for assessing prognosis of primary untreated adult patients with myelodysplastic syndromes (MDS). To refine the IPSS, MDS patient databases from international institutions were coalesced to assemble a much larger combined database (Revised-IPSS [IPSS-R], n = 7012, IPSS, n = 816) for analysis. Multiple statistically weighted clinical features were used to generate a prognostic categorization model. Bone marrow cytogenetics, marrow blast percentage, and cytopenias remained the basis of the new system. Novel components of the current analysis included: 5 rather than 3 cytogenetic prognostic subgroups with specific and new classifications of a number of less common cytogenetic subsets, splitting the low marrow blast percentage value, and depth of cytopenias. This model defined 5 rather than the 4 major prognostic categories that are present in the IPSS. Patient age, performance status, serum ferritin, and lactate dehydrogenase were significant additive features for survival but not for acute myeloid leukemia transformation. This system comprehensively integrated the numerous known clinical features into a method analyzing MDS patient prognosis more precisely than the initial IPSS. As such, this IPSS-R should prove beneficial for predicting the clinical outcomes of untreated MDS patients and aiding design and analysis of clinical trials in this disease.
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            The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

            The upcoming 5th edition of the World Health Organization (WHO) Classification of Haematolymphoid Tumours is part of an effort to hierarchically catalogue human cancers arising in various organ systems within a single relational database. This paper summarizes the new WHO classification scheme for myeloid and histiocytic/dendritic neoplasms and provides an overview of the principles and rationale underpinning changes from the prior edition. The definition and diagnosis of disease types continues to be based on multiple clinicopathologic parameters, but with refinement of diagnostic criteria and emphasis on therapeutically and/or prognostically actionable biomarkers. While a genetic basis for defining diseases is sought where possible, the classification strives to keep practical worldwide applicability in perspective. The result is an enhanced, contemporary, evidence-based classification of myeloid and histiocytic/dendritic neoplasms, rooted in molecular biology and an organizational structure that permits future scalability as new discoveries continue to inexorably inform future editions.
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              International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data

              The classification of myeloid neoplasms and acute leukemias was last updated in 2016 within a collaboration between the World Health Organization (WHO), the Society for Hematopathology, and the European Association for Haematopathology. This collaboration was primarily based on input from a clinical advisory committees (CACs) composed of pathologists, hematologists, oncologists, geneticists, and bioinformaticians from around the world. The recent advances in our understanding of the biology of hematologic malignancies, the experience with the use of the 2016 WHO classification in clinical practice, and the results of clinical trials have indicated the need for further revising and updating the classification. As a continuation of this CAC-based process, the authors, a group with expertise in the clinical, pathologic, and genetic aspects of these disorders, developed the International Consensus Classification (ICC) of myeloid neoplasms and acute leukemias. Using a multiparameter approach, the main objective of the consensus process was the definition of real disease entities, including the introduction of new entities and refined criteria for existing diagnostic categories, based on accumulated data. The ICC is aimed at facilitating diagnosis and prognostication of these neoplasms, improving treatment of affected patients, and allowing the design of innovative clinical trials.
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                Author and article information

                Contributors
                lionel.ades@aphp.fr
                shahram.kordasti@kcl.ac.uk
                Journal
                Hemasphere
                Hemasphere
                10.1002/(ISSN)2572-9241
                HEM3
                HemaSphere
                John Wiley and Sons Inc. (Hoboken )
                2572-9241
                15 May 2024
                May 2024
                : 8
                : 5 ( doiID: 10.1002/hem3.v8.5 )
                : e64
                Affiliations
                [ 1 ] Humanitas Clinical and Research Center–IRCCS & Department of Biomedical Sciences Humanitas University Milan Italy
                [ 2 ] Comprehensive Cancer Centre, King's College London UK
                [ 3 ] Hématologie seniors Hôpital Saint‐Louis, Assistance Publique des Hôpitaux de Paris (APHP) Paris France
                [ 4 ] INSERM UMR_S1160, Institut de Recherche Saint Louis Université Paris Cité Paris France
                [ 5 ] Research Group of Molecular Immunology Francis Crick Institute London UK
                [ 6 ] Department of Medicine 1, Haematology, Cellular Therapy, Hemostaseology and Infectious Diseases University Medical Center Leipzig Leipzig Germany
                [ 7 ] Department of Clinical Biochemistry Bispebjerg and Frederiksberg Hospital Copenhagen Denmark
                [ 8 ] Department of Pathology, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
                [ 9 ] Hematology Branch, National Heart, Lung and Blood Institute Bethesda Maryland USA
                [ 10 ] Imperial College London London UK
                [ 11 ] Université Paris Cité, CNRS, INSERM, Institut Cochin Paris France
                [ 12 ] Centre for Clinical Haematology, University Hospitals of Birmingham Birmingham UK
                [ 13 ] Cell & Developmental Biology Vanderbilt University School of Medicine Nashville Tennessee USA
                [ 14 ] Pathology, Microbiology and Immunology, Vanderbilt University Medical Center Nashville Tennessee USA
                [ 15 ] Vanderbilt‐Ingram Cancer Center, Vanderbilt University Medical Center Nashville Tennessee USA
                [ 16 ] Department of Clinical and Molecular Sciences Università Politecnica delle Marche Ancona Italy
                [ 17 ] Moffitt Cancer Center, Malignant Hematology Department Tampa USA
                [ 18 ] Universidade Católica Portuguesa Faculdade de Medicina Portugal
                [ 19 ] Universidade Católica Portuguesa, Centro de Investigação Interdisciplinar em Saúde Portugal
                [ 20 ] Medical Clinic I, University Hospital Carl Gustav Carus, TU Dresden Dresden Germany
                [ 21 ] Division of Cancer Sciences The University of Manchester Manchester UK
                [ 22 ] The Christie NHS Foundation Trust Manchester UK
                [ 23 ] Immunophenotyping Laboratory (Synnovis Analytics LLP) Southeast Haematological Malignancy Diagnostic Service, King's College Hospital London UK
                [ 24 ] University of Texas MD Anderson Cancer Center Houston, Texas USA
                [ 25 ] Hematology Department, Vall d'hebron University Hospital, Vall d'hebron Institut of Oncology (VHIO) Vall d'Hebron Barcelona Hospital Campus Barcelona Spain
                [ 26 ] Department of Haematology University Hospital of Wales Cardiff UK
                [ 27 ] Vanderbilt University Medical Center Nashville Tennessee USA
                [ 28 ] Laboratoire d'Immunologie et d‘Histocompatibilité, Assistance Publique des Hôpitaux de Paris (APHP), Hôpital Saint‐Louis Paris France
                [ 29 ] Institut Carnot OPALE, Institut de Recherche Saint‐Louis, Hôpital Saint‐Louis Paris France
                [ 30 ] Assistance Publique‐Hôpitaux de Paris Centre, Hôpital Cochin Paris France
                [ 31 ] Section for Hematology, Department of Medicine Haukeland University Hospital Bergen Norway
                [ 32 ] Department of Clinical Science Faculty of Medicine, University of Bergen Bergen Norway
                [ 33 ] Department of Haematology King's College Hospital, Denmark Hill London UK
                [ 34 ] Haematology Department Guy's and St Thomas NHS Trust London UK
                [ 35 ] MLL Münchner Leukämielabor Munich Germany
                [ 36 ] Hematopoietic Stem Cell Laboratory Francis Crick Institute London UK
                [ 37 ] Department of Hematology, Cancer Center Amsterdam Amsterdam University Medical Centers, location VU University Medical Center Amsterdam The Netherlands
                [ 38 ] Institute of Immunology and Immunotherapy University of Birmingham Birmingham UK
                [ 39 ] Myelodysplastic Syndrome Unit, Hematology Division Azienda Ospedaliero‐Universitaria Careggi, University of Florence Florence Italy
                [ 40 ] Department of Hematology, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
                [ 41 ] Biotech Research and Innovation Center (BRIC) University of Copenhagen Copenhagen Denmark
                [ 42 ] Department of Clinical Medicine, Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark
                [ 43 ] Hematology Department Hospital da Luz Lisboa Lisboa Portugal
                [ 44 ] Deanery Faculdade de Medicina, UCP Lisboa Portugal
                [ 45 ] Leeds Teaching Hospital Leeds UK
                Author notes
                [*] [* ] Correspondence: Lionel Adès ( lionel.ades@ 123456aphp.fr ); Shahram Kordasti ( shahram.kordasti@ 123456kcl.ac.uk )

                [*]

                Cristina A. Tentori and Lin P. Zhao are Joint first authors.

                [**]

                Matteo G. Della Porta, Catherine Cargo, Uwe Platzbecker, and Shahram Kordasti are Joint senior authors.

                [ † ]

                Lionel Adès and Shahram Kordasti are Joint corresponding authors.

                Author information
                http://orcid.org/0000-0002-4735-5226
                http://orcid.org/0000-0002-1535-9601
                http://orcid.org/0000-0002-0347-4207
                Article
                HEM364
                10.1002/hem3.64
                11096644
                38756352
                103e3bf8-85a2-44a7-a01a-187268c4184f
                © 2024 The Authors. HemaSphere published by John Wiley & Sons Ltd on behalf of European Hematology Association.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 31 January 2024
                : 03 March 2024
                Page count
                Figures: 5, Tables: 4, Pages: 16, Words: 10436
                Funding
                Funded by: The CRUK City of London Centre Award
                Award ID: CTRQQR‐2021/100004
                Categories
                Hematopoiesis
                Guidelines ‐ Consensus‐based
                Guidelines ‐ Consensus‐based
                Custom metadata
                2.0
                May 2024
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.4.3 mode:remove_FC converted:16.05.2024

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