Injection-site reactions upon Kineret (anakinra) administration: experiences and explanations

Anakinra is a recombinant form of the human interleukin-1 receptor antagonist (IL-1Ra), r-metHuIL-1Ra, which is produced by recombinant DNA technology in an E. coli expression system. Anakinra is identical to native human IL-1Ra, except for the addition of a single methionine residue at its amino terminus [1]. Therapeutically, anakinra neutralises the biological activity of IL-1α and β by competitively inhibiting the two cytokines binding to the IL-1 receptor [2]. The maintenance of balance between IL-1 and IL-1Ra is thought to be important in preventing the development of inflammatory arthritis. Kineret is indicated for the treatment of rheumatoid arthritis in adult patients, in the European Union in combination with methotrexate in patients with inadequate response to methotrexate alone, in the United States also as monotherapy in patients failing at least one disease-modifying anti-rheumatic drug (DMARD). The recommended dose of Kineret is 100 mg administered once daily via subcutaneous injection.

Injection-site reactions (ISR), often defined as a constellation of symptoms including swelling, erythema, pruritus and pain around the site of injection, is a common adverse event associated with different kinds of biologic therapies [3], and can present a challenge to patients. ISRs are the most common and consistently reported treatment-related adverse events associated with Kineret. These are typically characterised by one or more of erythema, ecchymosis, inflammation and pain. In a review of five clinical trials, at doses of 50–150 mg/day, the reported rates of ISRs were 71% for the anakinra-treated groups versus 28% for patients receiving placebo [4]. The median duration of the above-mentioned typical symptoms was 14–28 days. The development of ISRs in patients who had not previously experienced ISRs was uncommon after the first month of therapy. A summary of ISR frequencies in some of the clinical studies with Kineret is presented in Table 1.

Early observations, in clinical trials with Kineret, indicated that a substantial amount of patients had skin reactions varying in intensity from mild to severe. This prompted studies in both humans and rats in order to investigate if vehicle and/or protein were capable of inducing non-immunologically mediated cutaneous mast cell degranulation [5]. Healthy volunteers received daily injections of large doses (1 ml of up to 200 mg/ml) of IL-1Ra for 28 days. Intradermal testing after 28 injections demonstrated that the response (erythema and oedema) for both vehicle alone and rhuIL-1Ra in vehicle generally followed the same pattern as that observed in histamine-injected positive control sites. In rats, an intradermal testing assay was used where extravasation of blue dye (injected in the tail vein) was assessed 30 min after intradermal injections of test solutions. All test solutions, which consisted of the various components of the Kineret vehicle, induced permeability changes that were significantly greater than those occurring with PBS alone. Changing the vehicle to PBS significantly reduced the reactivity from that occurring with rhuIL-1Ra in citrate buffer. However, the permeability increase was still higher over that occurring with PBS alone. Concurrent administration of diphenhydramine (100 μg), an anti-histamine, and rhuIL-1Ra in citrate buffer totally eliminated the permeability increase. Clearly, the results of the study show that the components of the vehicle have the potential to induce mast cell degranulation. But the vehicle is not the sole cause of the reactions since patients given lower doses (1 ml of 20 mg/ml) of rhuIL-1Ra in vehicle have milder reactions. Thus, the combination of vehicle constituents and a high protein concentration in the syringe give rise to mast cell degranulation upon subcutaneous injection [5]. In one of the dose-finding studies with Kineret [6], it was also noted that the injection-site reactions were dose related. ISRs were experienced by 28% of subjects in the placebo group and by 19, 38, 56, 64 and 63% in the groups receiving anakinra at 0.04, 0.1, 0.4, 1.0 and 2.0 mg/kg, respectively.

The placebo used in all clinical trials performed with Kineret has consisted of the vehicle, i.e. the formulated solution without protein. A considerable amount of patients receiving placebo have also reported ISRs (see above). In commercially available Kineret syringes, anakinra is formulated in 10 mM sodium citrate, 140 mM NaCl, 0.5 mM EDTA, and polysorbate 80 and has pH 6.5. The protein concentration in the Kineret syringe is 100 mg/0.67 ml, equivalent to 150 mg/ml. Potential reasons for pain upon injection can be related to buffer (citrate), non-physiological pH (6.5 vs. 7.2) and the presence of the surfactant polysorbate 80.

The formulation strategy is primarily to achieve stability of the protein, and the use of citrate in the Kineret formulation has indeed structural biologic reasons. Highly concentrated IL-1Ra solutions are prone to aggregate at elevated temperature which is due to its predominant β-barrel structural fold. This protein aggregation can be suppressed by the presence of citrate in the solution. Phosphate, for instance, is an approximately fourfold weaker suppressant than citrate [7]. Sodium citrate is a common buffering agent for parenteral drugs formulated around pH 6 [8]. Furthermore, buffer concentration is a factor that must be considered when designing injectable presentations and low buffer concentrations (10 mM or lower) are recommended to reduce injection pain caused by buffer components [9].

It has previously been reported that a component part of an epoetin α preparation caused pain after subcutaneous injection. The pain experienced by the patients taking this epoetin α preparation was described as stinging, burning and itching, and it disappeared in most patients within 15 min. Differences in pain scores after subcutaneous injection of the epoetin α solution and its vehicle were assessed in a small trial with 36 volunteers, normal saline serving as placebo control. It turned out that pain scores with the vehicle or its citrate component were significantly higher than saline. The conclusion was that the local pain experienced after subcutaneous administration of the epoetin α solution was mainly due to the citrate component of the buffered solution [10]. In a study on subcutaneous delivery of typical buffers for human growth hormone preparations in humans, 0.3 ml of buffer with sodium citrate caused significantly more injection pain when compared to 0.3 ml saline [11].

Another component of the Kineret formulation is polysorbate 80. This substance is commonly used in many pharmaceuticals for its solubilising and stabilising effects. There are some case reports of patients who developed hypersensitivity reactions to erythropoietin. The subsequent skin testing and clinical course suggested that the reactions were due to the excipient polysorbate 80 [12]. Hence, in patients who develop hypersensitivity reactions after subcutaneous injections of biological drugs, a control of the presence of polysorbate 80 is valid.

The clinical experience indicates that there are two different types of ISRs in relation to injections of Kineret. One immediate, with a stinging and burning feeling, and one delayed, which presents with rash, swelling and pain. Up to 70% of patients experience an ISR and of those 95% are mild to moderate in severity. Onset of ISRs are generally within the first weeks of initiating therapy, and patients who do not experience an ISR within 4 weeks are unlikely to experience any ISR. The incidence rate of ISRs tends to diminish when patients are on concomitant oral steroids [13‐15].

The delayed type can present with a more severe reaction involving erythema, pruritus, swelling and pain, i.e. inflammatory lesions. Five patients were reported with cutaneous drug reactions due to anakinra in 2005 [16]. A histopathological study was performed on punch biopsy specimens of skin lesions. Within the dermis, the most striking feature was a prominent eosinophilic infiltrate with a tendency to concentrate around vessels and surrounding nerve fibres. An increased number of spindle-shaped mast cells and CD68+ dermal macrophages was also seen, characteristic of an allergic inflammation. The drug was discontinued in two patients (systemic reaction in one) while the other three completed the period of study but had occasional reappearances of drug eruptions. The delayed reaction may be treated with topical corticosteroids or anti-histamines and, in the vast majority of cases, disappears within 2 months.

The immediate ISRs with acute pain, experienced by many patients, cannot to the same extent be relieved by the remedies mentioned above. This reaction may, however, be alleviated by placing a cool pack on the injection site for a few minutes before and after the injection, thereby mildly anaesthetising the subcutaneous nerves. Many physicians assert that the immediate reaction is the one which is hardest to endure and is the cause of many drop outs from treatment with Kineret.

At our clinics (Nordström, Pettersson and Knight), we recently conducted a placebo-controlled trial with anakinra in adult-onset Still’s disease. During this study, patients were asked to apply a cool pack before and after the injection and to warm the syringe in their hand before injecting. Over 50% out of 12 patients experienced mild ISRs, all of whom required or were offered antihistamines and/or topical corticosteroids. Only one patient experienced an intermediate ISR that subsided during follow-up, and no patient withdrew from the study because of ISRs.

The clinical experiences put together can aid in the recommendation of remedies for the different kinds of ISRs. As described above, to alleviate the acute pain (stinging, burning) it is advised to warm the syringe, with its content, to room temperature before the injection and to apply a cold pack to the injection site 2–3 min before and immediately after the injection. The delayed reactions can be mitigated by application of topical hydrocortisone or anti-histamine cream, and it is recommended to alternate the injection sites to avoid recall reactions. The clinical understanding is also that they will disappear over time. In our opinion, the single most important measure to make patients manage both the acute and delayed ISRs is to inform in advance about the potential for such reactions. Convincing patients to remain motivated to push beyond the weariness of injections and injection-site reactions can be challenging, and these challenges have a major impact on adherence. This has been particularly true for patients suffering from multiple sclerosis, where disease-modifying therapies are often burdened with ISRs [17].