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      Outcomes after allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia patients with der(1;7)(q10;p10)

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          Abstract

          The prognosis of acute myeloid leukemia (AML) patients with der(1;7)(q10;p10) who underwent allogeneic hematopoietic stem cell transplantation (allo‐SCT) is unclear due to its rarity. We retrospectively analyzed 151 AML patients with der(1;7)(q10;p10) and compared the findings with those of 853 AML patients with monosomy 7 or chromosome 7q deletion (‐7/del(7q)) using Japanese nationwide registry data. The der(1;7)(q10;p10) group showed significantly better transplant outcomes than the ‐7/del(7q) group. In the multivariate analysis of the der(1;7)(q10;p10) group, additional chromosomal abnormalities and a poor performance status significantly influenced the survival. In conclusion, allo‐SCT is a feasible treatment option for AML patients with der(1;7)(q10;p10).

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          Most cited references15

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          Investigation of the freely available easy-to-use software ‘EZR' for medical statistics

          Y Kanda (2012)
          Although there are many commercially available statistical software packages, only a few implement a competing risk analysis or a proportional hazards regression model with time-dependent covariates, which are necessary in studies on hematopoietic SCT. In addition, most packages are not clinician friendly, as they require that commands be written based on statistical languages. This report describes the statistical software ‘EZR' (Easy R), which is based on R and R commander. EZR enables the application of statistical functions that are frequently used in clinical studies, such as survival analyses, including competing risk analyses and the use of time-dependent covariates, receiver operating characteristics analyses, meta-analyses, sample size calculation and so on, by point-and-click access. EZR is freely available on our website (http://www.jichi.ac.jp/saitama-sct/SaitamaHP.files/statmed.html) and runs on both Windows (Microsoft Corporation, USA) and Mac OS X (Apple, USA). This report provides instructions for the installation and operation of EZR.
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            The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.

            The World Health Organization (WHO) classification of tumors of the hematopoietic and lymphoid tissues was last updated in 2008. Since then, there have been numerous advances in the identification of unique biomarkers associated with some myeloid neoplasms and acute leukemias, largely derived from gene expression analysis and next-generation sequencing that can significantly improve the diagnostic criteria as well as the prognostic relevance of entities currently included in the WHO classification and that also suggest new entities that should be added. Therefore, there is a clear need for a revision to the current classification. The revisions to the categories of myeloid neoplasms and acute leukemia will be published in a monograph in 2016 and reflect a consensus of opinion of hematopathologists, hematologists, oncologists, and geneticists. The 2016 edition represents a revision of the prior classification rather than an entirely new classification and attempts to incorporate new clinical, prognostic, morphologic, immunophenotypic, and genetic data that have emerged since the last edition. The major changes in the classification and their rationale are presented here.
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              Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel.

              The first edition of the European LeukemiaNet (ELN) recommendations for diagnosis and management of acute myeloid leukemia (AML) in adults, published in 2010, has found broad acceptance by physicians and investigators caring for patients with AML. Recent advances, for example, in the discovery of the genomic landscape of the disease, in the development of assays for genetic testing and for detecting minimal residual disease (MRD), as well as in the development of novel antileukemic agents, prompted an international panel to provide updated evidence- and expert opinion-based recommendations. The recommendations include a revised version of the ELN genetic categories, a proposal for a response category based on MRD status, and criteria for progressive disease.
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                Author and article information

                Contributors
                ishiyama-knz@umin.ac.jp
                Journal
                EJHaem
                EJHaem
                10.1002/(ISSN)2688-6146
                JHA2
                EJHaem
                John Wiley and Sons Inc. (Hoboken )
                2688-6146
                06 November 2022
                February 2023
                : 4
                : 1 ( doiID: 10.1002/jha2.v4.1 )
                : 251-257
                Affiliations
                [ 1 ] Department of Hematology Kanazawa University Hospital Kanazawa Japan
                [ 2 ] Department of Hematopoietic Stem Cell Transplantation National Cancer Center Hospital Tokyo Japan
                [ 3 ] Department of Hematology Jyoban Hospital of Tokiwa Foundation Fukushima Japan
                [ 4 ] Division of Hematology Department of Internal Medicine Aichi Medical University Nagakute Japan
                [ 5 ] Hematology Division Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan
                [ 6 ] Department of Hematology Federation of National Public Service Personnel Mutual Aid Associations Toranomon Hospital Tokyo Japan
                [ 7 ] Department of Hematology and Oncology Tokai University School of Medicine Isehara Japan
                [ 8 ] Department of Hematology Kanagawa Cancer Center Yokohama Japan
                [ 9 ] Department of Hematology Hiroshima Red Cross Hospital and Atomic‐bomb Survivors Hospital Hiroshima Japan
                [ 10 ] Department of Hematology Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital Nagoya Japan
                [ 11 ] Department of Hematology Hyogo Medical University Hospital Hyogo Japan
                [ 12 ] Leukemia Research Center Saiseikai Maebashi Hospital Maebashi Japan
                [ 13 ] Department of Hematology National Hospital Organization Kumamoto Medical Center Kumamoto Japan
                [ 14 ] Division of Hematology‐Oncology Japanese Red Cross Society Narita Hospital Narita Japan
                [ 15 ] Japanese Data Center for Hematopoietic Cell Transplantation Nagoya Japan
                [ 16 ] Department of Registry Science for Transplant and Cellular Therapy Aichi Medical University School of Medicine Nagakute Japan
                [ 17 ] Department of Hematology and Cell Therapy Aichi Cancer Center Nagoya Japan
                Author notes
                [*] [* ] Correspondence

                Ken Ishiyama, Department of Hematology, Kanazawa University Hospital, 13‐1 Takaramachi, Kanazawa, Ishikawa 920‐8641, Japan.

                Email: ishiyama-knz@ 123456umin.ac.jp

                Author information
                https://orcid.org/0000-0002-9933-4638
                https://orcid.org/0000-0002-6189-0620
                https://orcid.org/0000-0002-4255-5616
                Article
                JHA2609
                10.1002/jha2.609
                9928652
                6b18af94-e3c5-4033-9350-1c618b43474d
                © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 October 2022
                : 20 October 2022
                Page count
                Figures: 1, Tables: 1, Pages: 7, Words: 3039
                Categories
                Short Report
                Short Reports
                Custom metadata
                2.0
                February 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.5 mode:remove_FC converted:14.02.2023

                additional chromosomal abnormalities,allogeneic hematopoietic stem cell transplantation,aml,der(1;7)(q10;p10)

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