Intravenous administration of anakinra in children with macrophage activation syndrome

Anakinra is a 17 KD recombinant, non-glycosylated Interleukin-1 (IL-1) receptor antagonist. Subcutaneous (SC) anakinra is used in the treatment of systemic JIA (SJIA) [1, 2]. Anakinra has also been described to be effective in the treatment of macrophage activation syndrome (MAS) secondary to sJIA as well as other rheumatic diseases like systemic lupus erythematosus (SLE) and Kawasaki Disease (KD) [2‐5]. Recent reports show anakinra can be effective in secondary hemophagocytic lymphohistiocytosis (sHLH) due to non-rheumatic diseases as well [6]. In some situations, such as thrombocytopenia, subcutaneous edema or in children in intensive care setting, it may be necessary to use intravenous (IV) administration of anakinra instead of SC anakinra. There have only been a few studies that evaluated the pharmacokinetics of IV anakinra in the past [7]. In the present era of COVID-19, high-dose anakinra has been shown to improve outcomes associated with hyper-inflammation observed both with SARS-CoV-2 infections and the newly described multisystem inflammatory syndrome in children (MIS-C) [8‐10]. We sought to describe our experience with IV anakinra in children with MAS at our institution prior to COVID-19 in order to guide clinicians wishing to consider this therapy for indications such as hyperinflammation seen with COVID-19 and MIS-C.

In collaboration with our hospital pharmacists, a protocol was designed for the use of IV anakinra in our center. The protocol outlines potential use of IV anakinra in patients with an underlying rheumatic condition (such as SJIA, SLE, KD) with features of MAS or secondary HLH. These patients may require high doses of anakinra, require multiple subcutaneous injections, may have subcutaneous edema, thrombocytopenia, or coagulopathy. For patients naïve to anakinra, the dose was started at 2 mg/kg and titrated up to a maximum of 100 mg IV every 12 h according to the patient’s clinical status. For patients already on maintenance anakinra and admitted to hospital, anakinra was titrated up to a maximum of 100 mg IV every 6 h according to the patient’s clinical status. The SC formulation was mixed in normal saline with 1 ml of normal saline per 1 mg of anakinra, administered IV over 30 min.

An IRB-approved retrospective chart review of various clinical and demographic variables via electronic medical record were identified for patients that had received IV anakinra at our institution between January 2017 and December 2019.

The duration of therapy, doses and outcome of the patients were recorded. MAS laboratory values as described by the Ravelli criteria [11] were identified prior to and 24 to 48 h after conclusion of administration of IV anakinra.

In all, 19 patients (9 male) received IV anakinra (Table 1). All patients met the 2016 Ravelli criteria for MAS [11], except patient #1 and #5, in whom a clinical decision was made to start anakinra due to rising ferritin and transaminases. Eleven patients were in a critical care setting during administration. Median age of our cohort was 13 years. Indication was MAS secondary to SJIA (n = 10), SLE (n = 3), sHLH (n = 5) and other (n = 1). All 5 patients with sHLH met 2004 HLH criteria [12] (Table 2). Maximum duration of therapy was 85 days. Median duration of therapy was 10 days. The initial dose of IV anakinra ranged from 1.7 to 10 mg/kg/day and the maximum dose of IV anakinra ranged from 4.2–15.4 mg/kg/day. One patient (#4) was already on 100 mg SQ Q12 of anakinra at home, and this was increased to 100 mg Q6 IV (20 mg/kg/day) to successfully treat an acute episode of MAS. The maximum frequency of administration was every 6 h. In most cases the general trend of the fibrinogen, ferritin, AST, and platelet count improved after initiation of IV anakinra. There were no reports of anaphylaxis or reactions associated with administration of IV anakinra.

Increased transaminases were noticed in patient #5 who received a maximum dose of 8 mg/kg/day (224 mg); discontinuation of anakinra resulted in normalization of AST and ALT. Five (26.3%) of the patients died from their underlying disease or complications. Other medications received by patients who died are depicted in Table 3. Patient #10 had SJIA and MAS; MAS laboratory parameters improved after IV anakinra administration. However, she developed Methicillin sensitive Staphylococcus aureus bacteremia (MSSA) leading to multi organ failure and cardiorespiratory arrest. Patient #14 had recurrent refractory ischemic strokes secondary to vasculitis of unknown etiology and multi-organ failure with MAS. Patient #17 with primary immune dysregulation (mutation in MUNC 13) died of overwhelming cytomegalovirus viremia (CMV) and MSSA bacteremia. Patient #18 with refractory HLH and CNS involvement also had overwhelming sepsis. Patient #19 with HLH status post BMT and recurrent CMV viremia died from multi organ failure, however anakinra had been used a year prior to her death. Three of these patients (#10, #18, #19) had improvement in the Ravelli MAS laboratory parameters in response to IV anakinra despite their fatal outcome.

Our experience with IV anakinra administration prior to the recent COVID-19 pandemic indicates that intravenously administered anakinra was overall safe and well tolerated with minimal adverse effects apart from one case of elevated transaminases, which is a known side effect of SC anakinra and described by Canna et al. [13]. There were no reported instances of anaphylaxis. It was effective for the treatment of MAS with improvement of laboratory parameters in most instances. Thus, IV anakinra may be an important therapeutic option for critically ill patients, although there is limited literary evidence regarding the pharmacokinetics, absorption, and efficacy of IV anakinra.

Prior studies of IV anakinra in sepsis have not shown an increase risk of adverse effects. In 1994, Fisher et al. [14] reported no statistically significant increase in survival time for Interleukin-1 antagonist treatment compared with placebo among all patients who received the study medication or among patients with sepsis. In a multicenter trial in 1997, Opal et al. [15] failed to demonstrate a statistically significant reduction in mortality when continuous IL-1 receptor antagonist infusions were compared with standard therapy in sepsis. In both these instances no excess adverse effects or microbial superinfections were attributed to the IL-1 inhibitor [14, 15]. In a large cohort of 763 patients, Shakoory et all in 2016 showed significant clinical improvement with treatment of IV anakinra vs placebo for sepsis patients with features of MAS [16].

Mehta et al. recently described high dose IV anakinra for MAS/HLH in cytokine storm syndromes [10]. They used IV anakinra in 39% of their patient population with cytokine storm and no adverse effects were seen. Cavalli et al. used IV anakinra at 10 mg/kg/day and showed improvement in COVID-19 associated hyperinflammation in 72% of their cohort [8]. Montegudo et al. used continuous Anakinra (2400 mg/day) in treatment of MAS/ sHLH with clinical improvement in 4/5 patients [17]. In a recent paper (December 2020) Kavirayani et al. successfully used IV anakinra at extremely high doses (48 mg/kg/day) for the treatment of non- familial CNS HLH even in the setting of intercurrent infections [18]. Thus, IV anakinra could be an option for treating COVID-19 associated hyperinflammatory state and/or cytokine storm in selected patients and appears to be well tolerated at high doses and in the setting of sepsis.

Limitations of our study include that it was retrospective in nature and only a relatively modest number of patients were included. However, we believe these cases are illustrative regarding the use of IV anakinra. Fatal outcome was observed in five patients in our series (26.3%) similar to findings noted by Eloseily et al. [19]. These patients either had severe, refractory disease or were immunosuppressed prior to IV anakinra exposure due to other medications/ post bone marrow transplant. Despite this, the laboratory indicators of MAS improved in three of the patients who succumbed to their illness.