Erythropoietin to Improve Critical Care Patient Outcomes

Anemia Clinical Trial

— EPO-ICU-FS  

Official title:

Erythropoietin to Improve Critical Care Patient Outcomes: Feasibility Study of a Multicenter, Randomized, Placebo-controlled Trial of Subcutaneous Erythropoietin Injection for Intensive Care Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05080049
• Other study ID #: EPO-ICU-FS
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: January 28, 2022
• Est. completion date: December 31, 2022

Study information

• Verified date: September 2022
• Source: University Hospital, Angers
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Recently, the french societies for critical care (SFAR and SRLF) produced guidelines for anemia treatment in critically ill patients that recommend the use of erythropoietin (EPO) in these patients, but the european society (ESICM) recommended against the use of EPO in this patients, despite recent meta analysis showing a lower mortality in patients treated with EPO. Nevertheless, RCT on EPO in the ICU are quite all, new data are thus needed. Before conducting a large study on EPO in anemic patients in the ICU, we propose to cinduct a feasability RCT to evaluate the feasability of such a study.

Description:

Anemia is very common in intensive care patients, affecting approximately two-thirds of patients on admission, with a mean admission hemoglobin (Hb) level of 11.0 g/dl. The severity of anemia is associated with increased morbidity and mortality. Its pathophysiology is complex, involving blood loss (from repeated blood sampling, invasive procedures, surgical interventions, etc.) and inflammation. The latter is responsible for a decrease in endogenous erythropoietin (EPO) production and a decreased bone marrow response, which can be very prolonged (half of the patients discharged from ICU with anemia are still anemic at 6 months of discharge, with low levels of EPO, compared to the observed Hb levels). On this basis, several randomized clinical trials (RCTs) evaluating the effect of EPO on the transfusion rate in this population were performed in the 1990s-2000s. The authors showed a modest reduction in blood transfusion, which was not considered clinically relevant in view of the cost of EPO at that time. Since then, meta-analyses evaluating the benefits and risks of EPO in intensive care patients suggest a positive impact of EPO on mortality. The largest, including 34 studies (and 930,470 patients) reports a reduction in the relative risk of mortality of 0.76, 95% CI [0.61 - 0.92]. Beyond the reduction in red blood cell transfusions, the benefit of EPO could be directly due to its erythropoietic effect (correction of anemia) and/or its anti-inflammatory/anti-apoptotic properties. Based on this literature, the French critical care societies have recently recommended the use of EPO. However, the European Society of Intensive Care Medicine (ESICM) recently recommended against the use of EPO, based on the same literature, but suggested that the benefit of EPO should be evaluated. Indeed, the main obstacle to recommending the use of EPO seems to be economic, whereas the arrival on the market of biosimilar molecules has significantly reduced these costs. Most of the trials on EPO in critical care patients (and included in the meta-analyses) are quite old (about 15 years) and none of them had mortality as primary endpoint. In addition, transfusion practices and the quality of blood products have changed significantly over the years. In this context of disagreement on the recommendations for the use of EPO in these patients, but of potential benefit on mortality, there is an urgent need to evaluate whether EPO decreases mortality in adult anemic patients admitted to intensive care. However, calculation of the number of patients needed to evaluate the benefit of EPO on mortality in this population yields a number of patients to be included of the order of 1800-2000 patients. Before considering the implementation of a multicenter study involving such a large number of patients, a pilot study evaluating the feasibility and inclusion capacity for such a study seems indispensable according to the latest CONSORT recommendations.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 42
• Est. completion date: December 31, 2022
• Est. primary completion date: September 2, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients (age > 18 years),
• admitted to intensive care for more than 72 hours and less than 7 days
• who have received invasive ventilatory support and/or treatment with a vasoactive agent for at least one day since admission
• with an Hb level < 12 g/dl,
• with consent from the patient or patient's relative (or emergency inclusion procedure).

Exclusion Criteria:

• Moribund patient,
• Current hospitalization for acute coronary syndrome,
• Recent history of thromboembolic event (< 3 months),
• Uncontrolled hypertension despite adequate antihypertensive therapy,
• Myelodysplasia or chronic pathology requiring iterative transfusions,
• EPO treatment within the last 30 days,
• Participation in another interventional trial of an erythropoiesis-stimulating agent or anemia treatment,
• Expected discharge from the intensive care unit within 24 hours,
• Known hypersensitivity to EPO or any of its components,
• A history of erythroblastopenia following erythropoietin therapy
• Pregnant, breast-feeding or parturient woman
• Person deprived of liberty by judicial or administrative decision
• Person under forced psychiatric care
• Person under a legal protection measure.

Related Conditions & MeSH terms

• Anemia
• Intensive Care

Intervention

Drug:
• Erythropoietin
Patients receive a subcutaneous injection of 40,000 IU of erythropoietin alfa or zêta, repeated weekly until Day 28 (if the hemoglobin level is <12 g/dl and the patient remains hospitalized). The study treatments are administered by an open-label nurse. In both groups, before each injection, iron deficiency (defined as reticulocyte Hb <29 pg, or hepcidin <41 µg/L, or ferritin <100 µg/L, or ferritin <300 µg/L with transferrin saturation <20%) is treated with intravenous iron infusion (depending on the product available at the center). A restrictive transfusion strategy is recommended as long as the patient remains in the ICU, according to recent recommendations. Six visits are scheduled: V1 for inclusion and the first injection, V2 at Day 7(±2 days) for the second injection, V3 at Day 14(±2 days) for the third injection, V4 at Day 21(±2 days) for the fourth injection, V5 at Day 28(±2 days) for the fifth injection.
• Placebo
In the control arm, patients receive a subcutaneous injection of placebo (0.9% NaCl) according to the same schedule. The study treatments are administered by an open-label nurse. In both groups, before each injection, iron deficiency (defined as reticulocyte Hb <29 pg, or hepcidin <41 µg/L, or ferritin <100 µg/L, or ferritin <300 µg/L with transferrin saturation <20%) is treated with intravenous iron infusion (depending on the product available at the center). A restrictive transfusion strategy is recommended as long as the patient remains in the ICU, according to recent recommendations. Six visits are scheduled: V1 for inclusion and the first injection, V2 at Day 7(±2 days) for the second injection, V3 at Day 14(±2 days) for the third injection, V4 at Day 21(±2 days) for the fourth injection, V5 at Day 28(±2 days) for the fifth injection.

Locations

Country	Name	City	State
France	Cholet Hospital	Cholet
France	UH Tours	Tours

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recruitment rate	=50% of eligible patients will need to be enrolled, but the trial will not be feasible if the inclusion rate is = 25% or less	90 days
Primary	Adherence to allocation groups	A high level of matching of randomization and group allocation should be achieved, with at least 85% of included patients receiving protocol-allocated treatment, but if = 65% patients receive protocol-allocated treatment, the trial is not feasible	90 days
Primary	Completion of follow-up of included patients	= 85% of patients should be followed through to the end of follow-up, but if <65% patients are followed through to the last visit, the protocol will not be feasible	90 days
Secondary	The proportion of patients lost to follow-up at each visit	The proportion of patients lost to follow-up at each visit	7, 14, 21, 28 and 90 days
Secondary	The rate of missing data for mortality outcome	The rate of missing data for mortality outcome	90 days
Secondary	The rate of compliance with the therapeutic protocol at each visit for inpatients	The rate of compliance with the therapeutic protocol at each visit for inpatients	7, 14, 21, and 28 days
Secondary	Mean serum hemoglobin value	Mean serum hemoglobin value	28 days
Secondary	ICU mortality	ICU mortality	up to 90 days
Secondary	Hospital mortality	Hospital mortality	up to 90 days
Secondary	ICU length of stay	ICU length of stay	up to 90 days
Secondary	Hospital length of stay	Hospital length of stay	up to 90 days
Secondary	Blood transfusion	Proportion of patients who received at least one red blood cell transfusion	90 days
Secondary	number of red blood cells transfused	number of red blood cells transfused	90 days
Secondary	90 days survival analysis	90 days survival analysis	90 days
Secondary	Occurrence of hospital readmission (censored at 90 days after inclusion),	at least one hospital readmission after the hospital discharge	90 days
Secondary	Number of days living at home (or previous place of living)	Number of days living at home (or previous place of living) at D90	90 days
Secondary	Quality of life measured by the EQ-5D 5L scale, EuroQol 5 dimensions	The value from this scale records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine'. The scale is rated from 0 to 100.	90 days
Secondary	Proportion of patients with a thromboembolic event	Thrombolic event: pulmonary embolism, venous or arterial thrombosis	90 days