Individualized recombinant human thrombomodulin (ART-123) administration in sepsis patients based on predicted phenotypes

Abstract

Letter to the editor Disseminated intravascular coagulation (DIC) is a relatively common complication of sepsis. The pathophysiology of septic DIC is associated with neutrophil extracellular trap (NET) formation [1] which results in subsequent thrombi formation known as immunothrombosis, especially in the liver. There are at least two known types of NETs; one type known as vital NETs is produced directly by activation of neutrophils on invasion by pathogens. The other type known as suicidal NETs is produced indirectly through the subsequent over-production of cytokines [2]. Vital NETs, which develop as an initial response to the pathogen, are shown to be suppressed by recombinant human thrombomodulin (ART-123), while suicidal NETs are not [1]. Therefore, ART-123 is potentially more effective when it is administered during the early phase of sepsis. In a phase 3 randomized controlled trial, ART-123 failed to show any differences in 28-day mortality compared to placebo [3]. In this trial, only patients with pre-existing coagulopathy were included based on the post hoc analysis of a phase 2 trial which had shown survival difference in this specific subgroup population. It is possible that the administration of ART-123 was too delayed to work effectively, since only patients with pre-existing coagulopathy were included and suicidal NETs were likely already activated in this population. Therefore, it is crucial to determine the cases that will benefit most from ART123 treatment during the early phase. There is increasing interest in the classification of sepsis [4] for personalized treatment options. More recently, a large, retrospective analysis based on machine learning method classified phenotypes of patients with sepsis into four clinical types (α, β, γ, and δ) that correlated with host response patterns using demographic data, physical examination findings, and laboratory data on arrival [5]. Of these, patients with the δ phenotype—characterized by liver dysfunction and shock—were more inclined to develop coagulopathy and had a higher mortality rate than those of patients with other phenotypes. Based on the findings of both studies, we hypothesize that patients with this phenotype are potentially most likely to benefit from ART-123. Since the phenotypes can be obtained before the patients develop coagulopathy, ART-123 can be administered during the early phase for those who are expected to develop coagulopathy. Further clinical trials with earlier intervention based on the clinical phenotyping for precision medicine are warranted to demonstrate mortality benefit of this theoretically effective medication for septic DIC.