Abstract

The discovery of biomarkers to predict the development of complications associated with hematopoietic stem cell transplantation (HSCT) offers a potential avenue for the early identification and treatment of these life-threatening consequences. Serum lactate dehydrogenase (sLDH) has been identified as a potential biomarker for determining the outcome of allogenic HSCT (allo-HSCT). A retrospective study was performed using data collected from 204 allo-HSCT recipient patients to examine the predictive value of sLDH levels pre- and post-allo-HSCT on patient survival, graft-versus-host-disease (GVHD) incidence, and time to platelet/white blood cells (WBC) engraftment. Our findings show that neither pre- (p= 0.61) nor post-transplantation (p= 0.55) sLDH levels were associated with GVHD incidence. However, elevated sLDH levels pre- and post-transplantation (≥ 386 and ≥ 409 IU/mL, respectively) were found to be adverse risk factors for patient survival (p= 0.16, p= 0.20, respectively). Furthermore, a median sLDH level ≥ 400 IU/mL from day +5 to day +15 post-transplantation had a significant positive association with enhanced time to platelet and white blood cell (WBC) engraftment, compared to patients with sLDH levels < 400 IU/mL (p< 0.001). Our data suggests that high sLDH levels pre- and post-allo-HSCT could be considered a predictor of poor patient survival. Furthermore, high levels of sLDH days 5-15 post-allo-HSCT could be associated with improved time to platelet and WBC engraftment; however, this appears to come at the cost of increased mortality risk.

Highlights

  • Allogeneic hematopoietic stem cell transplantation has been used as a curative treatment approach for a range of malignant and non-malignant diseases [1,2]

  • We further explored the prognostic value of Serum lactate dehydrogenase (sLDH) levels in the context of hematopoietic stem cell transplantation (HSCT)

  • We examined the association of sLDH levels preand post-transplantation on its ability to determine overall survival, GVHD incidence, and PLT/white blood cells (WBC) engraftment in patients receiving allo-HSCT

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Summary

Introduction

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has been used as a curative treatment approach for a range of malignant and non-malignant diseases [1,2] Despite the benefit this treatment strategy can provide, it is associated with. Donor/recipient HLA compatibility, comorbidities, conditioning regimens, and graft-versus-host-disease (GVHD) prophylaxis are understood to be the main contributing factors for determining the risk of sLDH levels in Pre- and Post-allo-HSCT complications associated with allo-HSCT. The discovery of biomarkers to predict the development of complications associated with hematopoietic stem cell transplantation (HSCT) offers a potential avenue for the early identification and treatment of these life-threatening consequences. High levels of sLDH days 5-15 post-allo-HSCT could be associated with improved time to platelet and WBC engraftment; this appears to come at the cost of increased mortality risk

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