EASIX and mortality after allogeneic stem cell transplantation

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作者
Thomas Luft
Axel Benner
Tobias Terzer
Sonata Jodele
Christopher E. Dandoy
Rainer Storb
Lambros Kordelas
Dietrich Beelen
Ted Gooley
Brenda M. Sandmaier
Mohamed Sorror
Markus Zeisbrich
Aleksandar Radujkovic
Peter Dreger
Olaf Penack
机构
[1] Medicine V,Department of Bone Marrow Transplantation, West German Cancer Centre
[2] University Hospital Heidelberg,Department of Nephrology
[3] Division of Biostatistics,Charité Universitätsmedizin Berlin, Hematology
[4] German Cancer Research Centre,undefined
[5] Oncology,undefined
[6] Hematology,undefined
[7] Cincinnati Children’s Hospital Medical Centre,undefined
[8] Fred Hutchinson Cancer Research Centre,undefined
[9] University of Washington,undefined
[10] University Hospital Essen,undefined
[11] University of Duisburg-Essen,undefined
[12] University of Heidelberg,undefined
[13] Oncology and Tumorimmunology,undefined
[14] Berlin-Brandenburg Centre for Regenerative Therapies,undefined
[15] Berlin Institute of Health,undefined
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摘要
Allogeneic stem cell transplantation (alloSCT) is an effective immunotherapy in patients with hematological malignancies. Endothelial dysfunction was linked to major complications after alloSCT. We asked the question if the “Endothelial Activation and Stress Index” (EASIX; [(creatinine × LDH) ÷ thrombocytes]) can predict mortality after alloSCT. We performed a retrospective cohort analysis in five alloSCT centers in the USA and Germany. EASIX was assessed prior to conditioning (EASIX-pre) and correlated with mortality in 755 patients of a training cohort in multivariable models. The predictive model established in the training cohort was validated in 1267 adult allo-recipients. Increasing EASIX-pre predicted lower overall survival (OS) after alloSCT, and successful model validation was achieved for the validation cohort. We found that EASIX-pre predicts OS irrespective of established scores. Moreover, EASIX-pre was also a significant prognostic factor for transplant-associated microangiopathy. Finally, EASIX-pre correlated with biomarkers of endothelial homeostasis such as CXCL8, interleukin-18, and insulin-like-growth-factor-1 serum levels. This study establishes EASIX-pre based on a standard laboratory biomarker panel as a predictor of individual risk of mortality after alloSCT independently from established clinical criteria.
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页码:553 / 561
页数:8
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