Early bilirubinemia after allogeneic stem cell transplantation-an endothelial complication.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
07 2021
Historique:
received: 31 03 2020
accepted: 01 12 2020
revised: 20 11 2020
pubmed: 1 2 2021
medline: 27 7 2021
entrez: 31 1 2021
Statut: ppublish

Résumé

Hyperbilirubinemia occurs frequently after allogeneic stem cell transplantation. Causes include primary liver damage and endothelial complications as major contributors. Here, we have investigated the impact of early bilirubinemia (EB) on posttransplant outcomes. Maximum total bilirubin levels (days 0-28) were categorized using maximally selected log rank statistics to identify a cut off for the endpoint non-relapse mortality (NRM) in a training cohort of 873 patients. EB above this cut off was correlated with NRM and overall survival (OS) and with pre- and posttransplant Angiopoietin-2, interleukin (IL)18, CXCL8 and suppressor of tumorigenicity-2 (ST2) serum levels, and the endothelial activation and stress index (EASIX). Clinical correlations were validated in a sample of 388 patients transplanted in an independent institution. The EB cut off was determined at 3.6 mg/dL (61.6 µM). EB predicted OS (HR 1.60, 95% CI 1.21-2.12, p < 0.001), and NRM (CSHR 2.14; 1.28-3.56, p = 0.004), also independent of typical endothelial complications such as veno-occlusive disease, refractory acute graft-versus-host disease, or transplant-associated microangiopathy. However, EB correlated with high Angiopoietin-2, EASIX-pre and EASIX-day 0, as well as increased levels of posttransplant CXCL8, IL18, and ST2. In summary, EB indicates a poor prognosis. The association of EB with endothelial biomarkers suggests an endothelial pathomechanism also for this posttransplant complication.

Identifiants

pubmed: 33517355
doi: 10.1038/s41409-020-01186-6
pii: 10.1038/s41409-020-01186-6
pmc: PMC8263345
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1573-1583

Subventions

Organisme : Wilhelm Sander-Stiftung (Wilhelm Sander Foundation)
ID : 2016.077.1
Organisme : EC | EC Seventh Framework Programm | FP7 Health (FP7-HEALTH - Specific Programme "Cooperation": Health)
ID : 306240
Organisme : China Scholarship Council (CSC)
ID : n.a.

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Auteurs

Hao Dai (H)

Epidemiology, German Cancer Research Centre, Heidelberg, Germany.

Olaf Penack (O)

Hematology, Oncology and Tumor Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Aleksandar Radujkovic (A)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

David Schult (D)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Joshua Majer-Lauterbach (J)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Igor Wolfgang Blau (IW)

Hematology, Oncology and Tumor Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Lars Bullinger (L)

Hematology, Oncology and Tumor Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Sihe Jiang (S)

Hematology, Oncology and Tumor Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Carsten Müller-Tidow (C)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Peter Dreger (P)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Thomas Luft (T)

Department of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany. thomas.luft@med.uni-heidelberg.de.

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