Use of Presepsin as a Marker for Immunotherapy Administration in Pneumonia (INSPIRE)

Immunotherapy Navigated by Serum Presepsin for Infections of the Respiratory Tract: the INSPIRE Double-blind, Randomized, Phase IIa Exploratory Trial.

The current study is an exploratory, phase IIa randomized clinical trial (RCT) aiming to evaluate if early presepsin increase coupled with early initiation of anakinra as an adjunct therapy to the standard-of-care treatment may improve outcomes of community-acquired pneumonia or hospital-acquired pneumonia.

Study Overview

• Status: Completed
• Conditions: Hospital-acquired Pneumonia; Community-acquired Pneumonia
• Intervention / Treatment: Drug: Placebo; Drug: Anakinra Prefilled Syringe

Detailed Description

Sepsis is a potentially lethal syndrome, which is characterized by the dysregulated response of the host to an infection. Due to its severity, sepsis should always be considered in patients with confirmed or suspected infection as it can rapidly progress to organ failure with poor prognosis. Conversely, patients with new-onset organ failure should be suspected for occult infection. Current epidemiology is suggesting an increase in the incidence of new cases. Sepsis has considerable economic burden on the community as septic patients merit higher-level of healthcare and prolonged hospital stay. Subsequently, prompt recognition and treatment are of essence in order to mitigate the overall toll.

In the past years, numerous efforts have been made to identify a biomarker that portends the presence of sepsis, but none has managed to consistently predict which patients will eventually develop this syndrome. This is largely attributed to still-unknown host and pathogen mechanisms by which the sepsis cascade is initiated. Therefore, further understanding of the pathophysiology is of paramount importance.

The pathogenesis of sepsis is multifaceted and includes immune, cardiovascular, coagulation and metabolic perturbations. Immune dysregulation is a well-established component that leads to tissue injury. Activation of the innate immunity is a crucial step in the sequence of the upcoming events. As such, if we manage to early recognize the activation of one specific immune pathway during the initial stages of sepsis in the human host and promptly commence immunotherapy directed against this specific pathway, we may prevent the cascade of events leading the patient to life-threatening organ dysfunction. This paradigm of timely intervention on the immune system upon early recognition of a specific pathway activation is the SAVE-MORE trial in COVID-19. Preemptive initiation of anakinra treatment guided by the early increase of the biomarker suPAR (soluble urokinase plasminogen activator receptor) well before clinical signs of deterioration develop led to a 64% overall improvement and a 55% relative decrease in mortality. This early personalized treatment was registered in December 2021 by the European Medicines Agency.

One similar cascade of events is happening in sepsis. Bacterial lipopolysaccharide (LPS) of the cell membrane of Gram-negative bacteria and danger-associated molecular patterns (DAMPs) like high-mobility group box-1 (HMGB1) and mitochondrial DNA (mtDNA) are recognized by toll-like receptors (TLRs). Cluster of Differentiation 14 (CD14) is the naturally occurring receptor of LPS on the surface of monocytes/macrophages and the regulator of TLR-4 signal transduction. In 2004, a novel form of CD14, named soluble CD14 subtype (sCD14-ST) or presepsin was found significantly increased in patients with sepsis. Numerous studies have validated its use as an early indicator of sepsis, but a definite cut-off value has not been established due to the heterogeneity in the study design, selection of patients and clinical context. Once LPS binds and activates TLR-4, production of interleukin (IL)-1 ensues. As a consequence, early detection of increased presepsin coupled with anakinra, one short half-life inhibitor of the activity of IL-1α and IL-1β, may be a promising personalized treatment strategy for sepsis.

In recent years, studies conducted by the Hellenic Sepsis Study Group have shown that presepsin levels over 350 pg/ml have satisfactory diagnostic and prognostic value for sepsis. In particular, results from the INTELLIGENCE-1 study showed that in patients with at least one of the qSOFA criteria, presepsin more than 350 pg/ml has a sensitivity for diagnosing sepsis and 28-day mortality of 80.2% and 91.5%, respectively. Similar results were reproduced by 2 more independent studies; INTELLIGENCE-2, which also included patients with qSOFA ≥ 1 and SAVE trial, which investigated patients with COVID-19.

On the other hand, presepsin's role in determining the appropriateness of treatment remains unclear. In a controlled clinical trial conducted by Hongli Xiao et al, presepsin was used at predefined cut-offs in order to modulate the duration of antimicrobial therapy in septic patients. The primary endpoints were the number of days free of antibiotics in a 28-day period and mortality on days 28 and 90. The results revealed significantly fewer days of antibiotic exposure to the presepsin group (14.54 days vs. 11.01 days; P < 0.001).

• Study Type: Interventional
• Enrollment (Actual): 60
• Phase: Phase 2

Contacts and Locations

Study Locations

• Greece
  • Athens, Greece
    • 1st Department of Internal Medicine, General Hospital of Eleusis THRIASIO
  • Athens, Greece, 12462
    • 4th Department of Internal Medicine, "Attikon" University Hospital, National and Kapodistrian University of Athens, Medical School
  • Athens, Greece
    • 1st Department of Internal Medicine, General Hospital of Athens GENNIMATAS
  • Athens, Greece
    • 6th Department of Pulmonary Medicine, SOTIRIA General Hospital of Chest Diseases of Athens
  • Nikaia, Greece
    • 3rd Department of Internal Medicine, General Hospital of Nikaia AGIOS PANTELEIMON

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Age equal to or above 18 years
• Male or female gender
• In case of women of reproductive age, willingness to use dual contraceptive method during the study period
• Written informed consent provided by the patient. For subjects without decision-making capacity, informed consent must be obtained from a legally designated representative following the national legislation in the Member State where the trial is planned
• Community-acquired pneumonia or hospital-acquired pneumonia
• qSOFA score equal to 1
• Serum presepsin > 350 pg/ml

Exclusion Criteria:

• Age below 18 years
• Denial of written informed consent
• Any stage IV malignancy
• Any do not resuscitate decision
• Patients with PaO2/FiO2 less than 150 necessitating non-invasive ventilation or mechanical ventilation
• Hospitalization in Intensive Care Unit
• Known hypersensitivity to anakinra
• Oral or IV intake of corticosteroids at a daily dose equal to or greater than 0.4 mg/kg prednisone for a period greater than the last 15 days
• qSOFA score 0, 2 or 3
• Any anti-cytokine biological treatment for the last one month
• Pregnancy or lactation. Women of child-bearing potential will be screened by a urine pregnancy test before inclusion in the study
• Participation in any other interventional trial

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Placebo; Treatment Arm 1: patients receiving placebo (N/S 0.9% w/v) subcutaneously once daily for 10 days plus Standard of Care	Drug: Placebo; 0.67 ml N/S 0.9% w/v administration subcutaneously once daily for 10 days (at least 4 days); Other Names: NaCl
Active Comparator: Anakinra; Treatment Arm 2: patients receiving anakinra subcutaneously 100 mg once daily for 10 days plus Standard of Care	Drug: Anakinra Prefilled Syringe; Anakinra 100 mg administration subcutaneously once daily for 10 days (at least 4 days); Other Names: Kineret

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of Sequential Organ Failure Assessment score by day 7 or death by day 90.	Patients who meet any of the following are considered to meet this endpoint: i) increase of Sequential Organ Failure Assessment score by 2 or more points from day 1 (before start of the study drug) until day 7; ii) death by day 90. Higher scores of the Sequential Organ Failure Assessment score indicate worsening of organ function, where the lowest score is 0 and highest is 24 (death).	90 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of Sequential Organ Failure Assessment score	Change of Sequential Organ Failure Assessment score over all days of follow-up. Higher scores indicate worsening of organ function, where lowest score is 0 and highest is 24 (death).	28 days
28-day organ dysfunction	Incidence of specific organ dysfunction by day 28	28 days
Time to hospital discharge	Time until discharge from hospital	28 days
28-day mortality	Mortality by day 28	28 days
Time to inflammation discontinuation	Time until attenuation of sepsis-induced inflammation as defined by procalcitonin measurements	7 days
Concentration of presepsin	Change of concentration of presepsin from baseline until day 10	10 days
Change in concentration of cytokines	Comparison of change of cytokine function by measurement of macrophage-derived, Th-1, Th-2 and Th-17 - derived cytokines' concentration following stimulation of cultured peripheral blood mononuclear cells (PBMCs). The concentrations of these molecules will be measured by enzyme-linked immunosorbent assay (ELISA) on days 1, 4 and 7.	7 days
Concentration of endothelial dysfunction markers	Comparison of change of endothelial dysfunction markers from baseline by days 4 and 7 by measurement of Intercellular Adhesion Molecule 1 (ICAM-1), Vascular Cell Adhesion Molecule 1 (VCAM-1), and E-selectin concentrations by enzyme-linked immunosorbent assay (ELISA).	7 days
Change of Sequential Organ Failure Assessment score of screening failure subjects	Comparative progression into overall organ dysfunction by day 10 (defined as in the primary endpoint) between patients who failed screening because of presepsin 350 pg/ml or less and patients who were enrolled in the study and were allocated to Treatment Arm 1 (placebo).	10 days
28-day mortality of screening failure cases compared with placebo	Comparative 28-day mortality between patients who failed screening because of presepsin 350 pg/ml or less and patients who were enrolled in the study and were allocated to Treatment Arm 1 (placebo).	28 days
90-day mortality	Mortality by day 90	90 days

Collaborators and Investigators

• Sponsor: Hellenic Institute for the Study of Sepsis
• Investigators: Study Chair: Evangelos Giamarellos-Bourboulis, MD, PhD, Hellenic Institute for the Study of Sepsis

Study record dates

Study Major Dates

• Study Start (Actual): March 6, 2023
• Primary Completion (Actual): June 28, 2024
• Study Completion (Actual): June 28, 2024

Study Registration Dates

• First Submitted: March 2, 2023
• First Submitted That Met QC Criteria: March 14, 2023
• First Posted (Actual): March 27, 2023

Study Record Updates

• Last Update Posted (Actual): July 31, 2024
• Last Update Submitted That Met QC Criteria: July 30, 2024
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: pneumonia; sepsis; anakinra; presepsin; SOFA
• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Respiratory Tract Infections; Respiratory Tract Diseases; Lung Diseases; Disease Attributes; Cross Infection; Iatrogenic Disease; Healthcare-Associated Pneumonia; Pneumonia; Antirheumatic Agents; Interleukin 1 Receptor Antagonist Protein
• Other Study ID Numbers: INSPIRE; 2022-002390-28 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No