Plasma biomarkers of lower gastrointestinal and liver acute GVHD

Author:

Harris Andrew C.1,Ferrara James L. M.1,Braun Thomas M.2,Holler Ernst3,Teshima Takanori4,Levine John E.1,Choi Sung W.1,Landfried Karin3,Akashi Koichi4,Lugt Mark Vander1,Couriel Daniel R.1,Reddy Pavan1,Paczesny Sophie1

Affiliation:

1. Blood and Marrow Transplant Program and

2. Department of Biostatistics, The University of Michigan, Ann Arbor, MI;

3. Department of Hematology/Oncology, University Medical Center Regensburg, Regensburg, Germany; and

4. Center for Cellular and Molecular Medicine, Kyushu University Graduate School of Science, Fukuoka, Japan

Abstract

Abstract The lower gastrointestinal tract (LGI) and liver are the GVHD target organs most associated with treatment failure and nonrelapse mortality. We recently identified regenerating islet-derived 3-α (REG3α) as a plasma biomarker of LGI GVHD. We compared REG3α with 2 previously reported GI and liver GVHD diagnostic biomarkers, hepatocyte growth factor (HGF) and cytokeratin fragment 18, in 954 hematopoietic cell transplantation patients. All 3 biomarkers were significantly elevated in LGI GVHD compared with non-GVHD diarrhea; REG3α discerned LGI GVHD from non-GVHD diarrhea better than HGF and cytokeratin fragment 18. Although all 3 biomarkers predicted nonresponse to therapy at day 28 in LGI GVHD patients, only REG3α and HGF concentrations predicted 1-year nonrelapse mortality (P = .01 and P = .02, respectively). Liver GVHD without GI involvement at GVHD onset and non-GVHD liver complications were uncommon; all 3 biomarkers were elevated in liver GVHD, but did not distinguish GVHD from other causes of hyperbilirubinemia.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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