International, Multicenter Standardization of Acute Graft-versus-Host Disease Clinical Data Collection: A Report from the Mount Sinai Acute GVHD International Consortium

Andrew C. Harris(University of Utah), Rachel Young(Mount Sinai Hospital), Steven M. Devine(The Ohio State University), William J. Hogan(WinnMed), Francis Ayuk(Universität Hamburg), Udomsak Bunworasate(Chulalongkorn University), Chantiya Chanswangphuwana(Chulalongkorn University), Yvonne A. Efebera(The Ohio State University), Ernst Holler(University of Regensburg), Mark R. Litzow(WinnMed), Rainer Ordemann(TU Dresden), Muna Qayed(Emory University), Anne S. Renteria(Icahn School of Medicine at Mount Sinai), Ran Reshef(Columbia University Irving Medical Center), Matthias Wölfl(Universitätsklinikum Würzburg), Yi‐Bin Chen(Massachusetts General Hospital), Steven C. Goldstein(University of Michigan–Ann Arbor), Madan Jagasia(Vanderbilt University Medical Center), Franco Locatelli(Bambino Gesù Children's Hospital), Stephan Mielke(University of Würzburg), David Porter(University of Pennsylvania), Tal Schechter(Hospital for Sick Children), Zhanna Shekhovtsova, James L.M. Ferrara(Mount Sinai Hospital), John E. Levine(Icahn School of Medicine at Mount Sinai)
Biology of Blood and Marrow Transplantation
September 16, 2015
Cited by 943Open Access
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Abstract

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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