Acute GVHD, BK virus hemorrhagic cystitis and age are risk factors for transplant-associated thrombotic microangiopathy in adults

Author:

Vasu Sumithira1,Bostic Matthew1,Zhao Qiuhong1,Sharma Nidhi1ORCID,Puto Marcin2,Knight Samantha1,Scott Denise1,Guzman Rosalyn1,Kromer Meghan1,Tackett Karen1,Lind Kristin1,Knill Kathryn1,Watson Emily1,Wall Sarah1ORCID,Saad Ayman1ORCID,Choe Hannah1,Larkin Karilyn1ORCID,Brammer Jonathan1,Jaglowski Samantha1ORCID,Penza Sam1,Davies Stella M.3,Cataland Spero1

Affiliation:

1. Division of Hematology, and

2. Department of Pharmacy, The Ohio State University, Columbus, OH; and

3. Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children’s Hospital, Cincinnati, OH

Abstract

Abstract Hematopoietic cell transplantation–associated thrombotic microangiopathy (TMA) is a complication associated with higher nonrelapse mortality (NRM) in patients who undergo allogeneic transplant (HCT). Current classification criteria are not generally agreed on or validated, and the presence of confounding factors after transplant contribute to underdiagnosis or delayed diagnosis of TMA. We studied risk factors, incidence, and biomarkers of TMA in 119 adult allogeneic HCT recipients. Twenty-seven patients developed a clinically actionable phenotype of TMA (CA-TMA) and the incidence of CA-TMA was 22% by day 180. Among the 27 patients who developed CA-TMA, 10 developed it before the onset of acute graft-versus-host disease (aGVHD), and 17 patients developed it after the onset of aGVHD. We report for the first time that age >50 years, BK hemorrhagic cystitis, and other viral infections (CMV, HHV-6, or adenovirus) are risk factors for adult CA-TMA. Even after adjustment for aGVHD, CA-TMA was independently associated with significantly higher NRM. These data illustrate relationships between CA-TMA and aGVHD, describe new risk factors for CA-TMA and emphasizes the need to develop validated set of criteria for timely diagnosis.

Publisher

American Society of Hematology

Subject

Hematology

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