Endothelial Activation and Stress Index-Measured Pretransplantation Predicts Transplantation-Related Mortality in Patients with Thalassemia Major Undergoing Transplantation with Thiotepa, Treosulfan, and Fludarabine Conditioning.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
07 2022
Historique:
received: 11 02 2022
revised: 18 04 2022
accepted: 01 05 2022
pubmed: 14 5 2022
medline: 7 7 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

The use of thiotepa-treosulfan-fludarabine conditioning regimen and peripheral blood stem cell grafts is associated with improved outcomes of hematopoietic stem cell transplantation (HCT) in patients with high-risk thalassemia major. However, there remains a need to identify predictors of poor outcomes in this cohort to further optimize outcomes. The Endothelial Activation and Stress Index (EASIX) is a biomarker shown to predict survival in various settings, including graft-versus-host disease, veno-occlusive disease, and nonrelapse mortality following allogeneic HCT. In this retrospective analysis, we evaluated the role of EASIX-PreTx (measured before conditioning therapy) as a biomarker in predicting day +100 transplantation-related mortality (TRM+100) in 281 patients with thalassemia major who underwent HCT with a uniform conditioning regimen using thiotepa-treosulfan-fludarabine at our center between January 2012 and December 2019. The median patient age was 9 years (range, 1 to 25 years), and 109 (38.8%) were females. According to the Pesaro classification (with Vellore modification), 3 patients (1.1%) were class I, 34 (12.1%) were class II, 134 (47.7%) were class III low risk, and 110 (39.1%) were class III high risk. Stem cell donors were matched sibling (n = 218; 77.6%), matched related nonsibling (n = 23; 8.2%), or matched unrelated (n = 40; 14.2%). Five patients (1.8%) received a bone marrow graft, and the others received a peripheral blood stem cell graft. Thirty-eight patients (13.5%) had TRM+100. EASIX-PreTx was available for 184 patients (65.5%). The median EASIX-PreTx was significantly higher in patients with TRM+100 compared with those without TRM+100 (1.09 versus .75; P = .008). An EASIX-PreTx cutoff of .85 had 70.4% sensitivity and 62% specificity for predicting TRM+100. The TRM+100 for patients with EASIX-PreTx >.85 was significantly higher than those with EASIX <.85 (24.4% versus 7.5%; P = .003). In a uniform subgroup of class III patients undergoing allogeneic HCT (n = 156), EASIX-PreTx was an independent predictor of TRM+100.

Identifiants

pubmed: 35550442
pii: S2666-6367(22)01270-2
doi: 10.1016/j.jtct.2022.05.001
pii:
doi:

Substances chimiques

Thiotepa 905Z5W3GKH
treosulfan CO61ER3EPI
Vidarabine FA2DM6879K
Busulfan G1LN9045DK
fludarabine P2K93U8740

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

356.e1-356.e6

Informations de copyright

Copyright © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Uday P Kulkarni (UP)

Department of Haematology, Christian Medical College, Vellore, India.

Aswin Anand Pai (AA)

Department of Haematology, Christian Medical College, Vellore, India.

M L Kavitha (ML)

Department of Haematology, Christian Medical College, Vellore, India.

Sushil Selvarajan (S)

Department of Haematology, Christian Medical College, Vellore, India.

Sharon Lionel (S)

Department of Haematology, Christian Medical College, Vellore, India.

Anup J Devasia (AJ)

Department of Haematology, Christian Medical College, Vellore, India.

Anu Korula (A)

Department of Haematology, Christian Medical College, Vellore, India.

N A Fouzia (NA)

Department of Haematology, Christian Medical College, Vellore, India.

Eunice Sindhuvi (E)

Department of Haematology, Christian Medical College, Vellore, India.

Aby Abraham (A)

Department of Haematology, Christian Medical College, Vellore, India.

Alok Srivastava (A)

Department of Haematology, Christian Medical College, Vellore, India.

Vikram Mathews (V)

Department of Haematology, Christian Medical College, Vellore, India.

Biju George (B)

Department of Haematology, Christian Medical College, Vellore, India.

Poonkuzhali Balasubramanian (P)

Department of Haematology, Christian Medical College, Vellore, India. Electronic address: bpoonkuzhali@cmcvellore.ac.in.

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