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      PTCy versus ATG as graft-versus-host disease prophylaxis in mismatched unrelated stem cell transplantation

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          Abstract

          There is an increased risk of GVHD and of non-relapse mortality (NRM) after allogeneic stem cell transplantations (alloSCT) when mismatched unrelated donors (MMUD) are used. In Europe, it is standard practice to use rabbit anti-thymocyte globulin (rATG) to reduce the high NRM and GVHD risks after MMUD alloSCT. As an alternative to rATG, post-transplantation Cyclophosphamide (PTCy) is in increasing clinical use. It is currently impossible to give general recommendations regarding preference for one method over another since comparative evidence from larger data sets is lacking. To improve the evidence base, we analyzed the outcome of rATG vs. PTCy prophylaxis in adult patients with hematologic malignancies undergoing first peripheral blood alloSCT from MMUD (9/10 antigen match) between Jan 2018 and June 2021 in the database of the European Society for Blood and Marrow Transplantation (EBMT). We performed multivariate analyses using the Cox proportional-hazards regression model. We included 2123 patients in the final analyses (PTCy, n = 583; rATG, n = 1540). p values and hazard ratios (HR) presented here are multivariate outcomes. Two years after alloSCT we found a lower NRM in the PTCy group of 18% vs. 24.9% in the rATG group; p = 0.028, HR 0.74. Overall survival in the PTCy cohort was higher with 65.7% vs. 55.7% in the rATG cohort; p < 0.001, HR 0.77. Progression-free survival was also better in the PTCy patients with 59.1% vs. 48.8% when using rATG; p = 0.001, 0.78. The incidences of chronic GVHD and acute GVHD were not significantly different between the groups. We found significantly lower NRM as well as higher survival in recipients of peripheral blood alloSCTs from MMUD receiving PTCy as compared to rATG. The results of the current analysis suggest an added value of PTCy as GVHD prophylaxis in MMUD alloSCT.

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          A Proportional Hazards Model for the Subdistribution of a Competing Risk

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            National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2014 Diagnosis and Staging Working Group report.

            The 2005 National Institutes of Health (NIH) Consensus Conference proposed new criteria for diagnosing and scoring the severity of chronic graft-versus-host disease (GVHD). The 2014 NIH consensus maintains the framework of the prior consensus with further refinement based on new evidence. Revisions have been made to address areas of controversy or confusion, such as the overlap chronic GVHD subcategory and the distinction between active disease and past tissue damage. Diagnostic criteria for involvement of mouth, eyes, genitalia, and lungs have been revised. Categories of chronic GVHD should be defined in ways that indicate prognosis, guide treatment, and define eligibility for clinical trials. Revisions have been made to focus attention on the causes of organ-specific abnormalities. Attribution of organ-specific abnormalities to chronic GVHD has been addressed. This paradigm shift provides greater specificity and more accurately measures the global burden of disease attributed to GVHD, and it will facilitate biomarker association studies.
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              International, Multicenter Standardization of Acute Graft-versus-Host Disease Clinical Data Collection: A Report from the Mount Sinai Acute GVHD International Consortium.

              Acute graft-versus-host disease (GVHD) remains a leading cause of morbidity and nonrelapse mortality after allogeneic hematopoietic cell transplantation. The clinical staging of GVHD varies greatly between transplant centers and is frequently not agreed on by independent reviewers. The lack of standardized approaches to handle common sources of discrepancy in GVHD grading likely contributes to why promising GVHD treatments reported from single centers have failed to show benefit in randomized multicenter clinical trials. We developed guidelines through international expert consensus opinion to standardize the diagnosis and clinical staging of GVHD for use in a large international GVHD research consortium. During the first year of use, the guidance followed discussion of complex clinical phenotypes by experienced transplant physicians and data managers. These guidelines increase the uniformity of GVHD symptom capture, which may improve the reproducibility of GVHD clinical trials after further prospective validation.
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                Author and article information

                Contributors
                olaf.penack@charite.de
                Journal
                Blood Cancer J
                Blood Cancer J
                Blood Cancer Journal
                Nature Publishing Group UK (London )
                2044-5385
                15 March 2024
                15 March 2024
                December 2024
                : 14
                : 1
                : 45
                Affiliations
                [1 ]Medical Clinic, Department for Haematology, Oncology and Tumorimmunology, Charité Universitätsmedizin Berlin, ( https://ror.org/001w7jn25) Berlin, Germany
                [2 ]GRID grid.492743.f, EBMT Transplant Complications Working Party, ; Paris, France
                [3 ]GRID grid.462844.8, ISNI 0000 0001 2308 1657, EBMT Paris Study Office, Department of Haematology, Saint Antoine Hospital, INSERM UMR-S 938, , Sorbonne University, ; Paris, France
                [4 ]Anadolu Medical Center Hospital, Kocaeli, Turkey
                [5 ]Oslo University Hospital, Rikshospitalet, ( https://ror.org/00j9c2840) Oslo, Norway
                [6 ]GRID grid.14925.3b, ISNI 0000 0001 2284 9388, Gustave Roussy Cancer Campus, ; Villejuif, France
                [7 ]University Medical Center, Department for Stem Cell Transplantation, ( https://ror.org/021ft0n22) Hamburg, Germany
                [8 ]Hannover Medical School, ( https://ror.org/00f2yqf98) Hannover, Germany
                [9 ]GRID grid.460094.f, ISNI 0000 0004 1757 8431, ASST Papa Giovanni XXIII, ; Bergamo, Italy
                [10 ]GRID grid.6292.f, ISNI 0000 0004 1757 1758, IRCCS Azienda Ospedaliero-Universitaria di Bologna, ; Bologna, Italy
                [11 ]University of Muenster, ( https://ror.org/00pd74e08) Muenster, Germany
                [12 ]University of Heidelberg, ( https://ror.org/038t36y30) Heidelberg, Germany
                [13 ]GRID grid.412460.5, RM Gorbacheva Research Institute, , Pavlov University, ; St Petersburg, Russia
                [14 ]Department of Hematology, University Hospitals Leuven and KU Leuven, ( https://ror.org/05f950310) Leuven, Belgium
                [15 ]GRID grid.412210.4, ISNI 0000 0004 0397 736X, Department of Haematology, , University Hospital Centre Rijeka, ; Rijeka, Croatia
                Author information
                http://orcid.org/0000-0003-4876-802X
                http://orcid.org/0000-0001-5103-9966
                http://orcid.org/0000-0003-1544-9911
                http://orcid.org/0000-0002-7429-8570
                Article
                1032
                10.1038/s41408-024-01032-8
                10940681
                38485723
                570c0dbe-a2c6-433a-b0de-11fed1d7358b
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 18 December 2023
                : 4 March 2024
                : 5 March 2024
                Categories
                Article
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                © Springer Nature Limited 2024

                Oncology & Radiotherapy
                stem-cell research,translational research,graft-versus-host disease

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