Transplant-associated thrombotic microangiopathy in pediatric patients: pre-HSCT risk stratification and prophylaxis.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
27 04 2021
Historique:
received: 09 12 2020
accepted: 08 03 2021
entrez: 20 4 2021
pubmed: 21 4 2021
medline: 1 6 2021
Statut: ppublish

Résumé

Transplant-associated thrombotic microangiopathy (TA-TMA) is an endothelial injury syndrome that complicates hematopoietic stem cell transplant (HSCT). Morbidity and mortality from TA-TMA remain high, making prevention critical. We describe our retrospective single-center experience of TA-TMA after pediatric allogeneic HSCT and present a novel pre-HSCT risk-stratification system and prophylaxis regimen. From January 2012 through October 2019, 257 patients underwent 292 allogeneic HSCTs. Prospective risk stratification was introduced in December 2016. High-risk (HR) patients were treated with combination prophylaxis with eicosapentaenoic acid and N-acetylcysteine. The 1-year cumulative incidence of TA-TMA was 6.3% (95% confidence interval [CI], 3.2-9.4). Age ≥10 years, myeloablative conditioning with total body irradiation, HLA mismatch, diagnosis of severe aplastic anemia or malignancy, prior calcineurin inhibitor exposure, and recipient cytomegalovirus seropositivity were found to be pre-HSCT risk factors for development of TA-TMA. Before routine prophylaxis, TA-TMA rates were significantly different between the HR and standard-risk groups, at 28.2% (95% CI, 0-12.7) vs 3.2% (0.1-6.3), respectively (P < .001). After introduction of prophylaxis, the 1-year cumulative incidence of TA-TMA in the HR group decreased to 4.5% (95% CI, 0-13.1; P = .062, compared with the incidence before prophylaxis). Multicenter pediatric studies are needed to validate these risk criteria and to confirm the efficacy of the prophylactic regimen.

Identifiants

pubmed: 33877298
pii: S2473-9529(21)00268-8
doi: 10.1182/bloodadvances.2020003988
pmc: PMC8095147
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2106-2114

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Christine S Higham (CS)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

Griffin Collins (G)

Division of Pediatric Hematology and Oncology, and.

Kristin A Shimano (KA)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

Alexis Melton (A)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

Sandhya Kharbanda (S)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

Lena E Winestone (LE)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

James N Huang (JN)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.
Division of Pediatric Hematology and Oncology, and.

Jasmeen Dara (J)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

Janel R Long-Boyle (JR)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.
Department of Clinical Pharmacy, Benioff Children's Hospital, University of California San Francisco, San Francisco, CA.

Christopher C Dvorak (CC)

Division of Pediatric Allergy, Immunology, and Bone Marrow Transplant.

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