Journal for ImmunoTherapy of Cancer (Jan 2024)

Endothelial Activation and Stress Index (EASIX) to predict mortality after allogeneic stem cell transplantation: a prospective study

  • Axel Benner,
  • Peter Dreger,
  • Grzegorz W Basak,
  • Christian Koenecke,
  • Olaf Penack,
  • Christophe Peczynski,
  • Lucia López Corral,
  • Ivan Moiseev,
  • Hélène Schoemans,
  • Zinaida Peric,
  • Thomas Luft,
  • Simona Sica,
  • Mutlu Arat,
  • Maija Itäla-Remes,
  • Nicolaas P M Schaap,
  • Michal Karas,
  • Ludek Raida,
  • Thomas Schroeder,
  • Elisabetta Metafuni,
  • Tulay Ozcelik,
  • Brenda M Sandmaier,
  • Lambros Kordelas

DOI
https://doi.org/10.1136/jitc-2023-007635
Journal volume & issue
Vol. 12, no. 1

Abstract

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Background We previously reported that the “Endothelial Activation and Stress Index” (EASIX; ((creatinine×lactate dehydrogenase)÷thrombocytes)) measured before start of conditioning predicts mortality after allogeneic hematopoietic stem cell transplantation (alloSCT) when used as continuous score. For broad clinical implementation, a prospectively validated EASIX-pre cut-off is needed that defines a high-risk cohort and is easy to use.Method In the current study, we first performed a retrospective cohort analysis in n=2022 alloSCT recipients and identified an optimal cut-off for predicting non-relapse mortality (NRM) as EASIX-pre=3. For cut-off validation, we conducted a multicenter prospective study with inclusion of n=317 first alloSCTs from peripheral blood stem cell in adult patients with acute leukemia, lymphoma or myelodysplastic syndrome/myeloproliferative neoplasms in the European Society for Blood and Marrow Transplantation network.Results Twenty-three % (n=74) of alloSCT recipients had EASIX-pre ≥3 taken before conditioning. NRM at 2 years was 31.1% in the high EASIX group versus 11.5% in the low EASIX group (p<0.001). Patients with high EASIX-pre also had worse 2 years overall survival (51.6% vs 70.9%; p=0.002). We were able to validate the cut-off and found that EASIX ≥3 was associated with more than twofold increased risk for NRM in multivariate analysis (HR=2.18, 95% CI 1.2 to 3.94; p=0.01). No statistically significant difference could be observed for the incidence of relapse.Conclusions The results of this study provide a prospectively validated standard laboratory biomarker index to estimate the transplant-related mortality risk after alloSCT. EASIX ≥3 taken before conditioning identifies a population of alloSCT recipients who have a more than twofold increased risk of treatment-related mortality.