Guidelines for the proper use of etanercept in Japan

Abstract

Application of biological agents targeting inflammatory cytokines such as tumor necrosis factor-α (TNF-α) dramatically caused a paradigm shift in the treatment of rheumatoid arthritis (RA). Infliximab, a chimeric anti-TNF-α monoclonal antibody, has initially been introduced to Japan in 2003 and shown to be dramatically effective in alleviating arthritis refractory to conventional treatment. However, serious adverse events such as bacterial pneumonia, tuberculosis, and Pneumocystis jiroveci pneumonia were reported to be in relatively high incidence; i.e., 2%, 0.3%, and 0.4%, respectively, in a strict postmarketing surveillance of an initial 4000 cases in Japan. Etancercept, a recombinant chimeric protein consisting of p75 TNF-α receptor and human IgG, was subsequently introduced to Japan in March of 2005. We therefore drew up treatment guidelines for the use of etanercept to avoid potential serous adverse events, since only approximately 150 cases have been included in the clinical study of etanercept in Japan. The guidelines were initially designed by the principal investigators (N.M, T.T., K.E.) of rheumatoid arthritis study groups of the Ministry of Health, Labor and Welfare (MHLW), Japan, and finally approved by the board of directors of the Japan College of Rheumatology. The MHLW assigned a duty to the pharmaceutical companies to perform a complete postmarketing surveillance of an initial 3000 cases to explore any adverse events, and this was performed according to the treatment guidelines shown in this article.

Introduction

In recent years, there has been a paradigm shift in the treatment of rheumatoid arthritis (RA). It is mostly attributed to the introduction of biological agents targeting inflammatory cytokines. Biological agents have approved and marketed for the treatment of RA in Europe and the United States include anti-tumor necrosis factor-α (TNF-α) antibodies such as infliximab (Remicade) adalimumab (Humira), soluble TNF-α receptor etanercept (Enbrel), and interleukin (IL)-1 receptor antagonist anakinra (Kineret). Among these, etanercept has drawn particular attention as a highly effective and safe biological product in the treatment of RA; it was approved in January 2005 in Japan.

Efficacy and adverse events of etanercept

Etanercept is a recombinant chimeric protein consisting of two molecules of p75 and the Fc portion of human IgG1 and is produced by introducing the fusion gene into Chinese hamster ovary cells (molecular weight, approximately 150kDa; total amino acid residues, 934). As compared with the natural-occurring soluble TNF-α receptor, etanercept showed 50-fold greater binding to TNF-α, 100- to 1000-fold greater biological activity, and 5- to 8-fold longer plasma half-life; therefore, treatment of RA with etanercept has been conducted.1

In a phase III study in the United States involving 234 patients with active RA who were resistant to disease-modifying antirheumatic drugs (DMARDs) including methotrexate (MTX), treatment with etanercept 25mg showed significantly greater efficacy than etanercept 10mg or placebo.1 Analysis of adverse events revealed that the incidence of injection-site reactions was significantly higher in the 25-mg dose group than other dose groups and that the active treatment groups had a higher incidence of infections, i.e., upper respiratory tract infections, than the placebo group.

In a double-blind study of concomitant MTX, 89 patients with active RA who had been treated with MTX for at least 6 months received either etanercept 25 mg or placebo twice a week subcutaneously in addition to MTX, resulting in improvement in a 20% American College of Rheumatology (ACR 20) response in 71% of patients receiving etanercept and an ACR 50 improvement in 39% of patients receiving etanercept. Moreover, there were no significant differences in incidence of adverse events such as infections between the two groups.2

On the basis of these results, etanercept was approved as a treatment for RA by the Federal Drug Administration (FDA) in the United States in November 1998. More than 6 years after its approval in the United States, the drug was approved in January 2005 and has been marketed since the end of March 2005 in Japan.

The most significant benefit of etanercept is to inhibit the progression of joint destruction. Its efficacy has been demonstrated to be far superior to that of MTX, which is known to have the potent effect of slowing the progression of joint destruction.3 The remarkable effectiveness of etanercept has been shown particularly in the recently reported TEMPO (Trial of Etanercept and Methotrexate with Radiographic Patient Outcomes).4 In this trial, 686 patients with RA who were resistant to one or more DMARDs other than MTX received one of the following three treatments for 2 years: MTX alone, etanercept alone, or etanercept plus MTX. The primary efficacy endpoint was the numeric index of the ACR response (ACR-N) area under the curve (ACR-AUC) over the first 24 weeks. The primary endpoint did not differ significantly between the MTX monotherapy group and etanercept monotherapy group; however, the etanercept plus MTX group had significantly higher ACR-AUC values than the two monotherapy groups. The proportion of patients achieving ACR 50, a clinically meaningful efficacy, at 2 years was 71% in the etanercept plus MTX group as compared with 42% in the MTX monotherapy group and 54% in the etanercept group, indicating greater efficacy of the combination of etanercept and MTX. Moreover, the change in total Sharp Score at 1 year of treatment was −0.54 in the etanercept plus MTX group as compared with +2.8 in the MTX monotherapy group and +0.52 in the etanercept group, suggesting the possibility that the combination may inhibit the progression of joint destruction and even heal the condition.

Frequently observed adverse events include injectionsite reactions, which are characterized by erythema with pruritus, swelling, or pain at the injection sites. Most reactions disappear with only topical treatments such as antihistamines.

The most careful attention should be given to monitoring for infections. Among the more than 1100 patients receiving long-term treatment for at least 6 months, 50 experienced serious infections such as pyelonephritis, bronchitis, septic arthritis, and abscess formation, which were caused by various types of organisms including bacteria, fungi, and Pneumocystis jiroveci. Etanercept may mask clinical symptoms characteristic of infections, such as fever and chills, and inhibit the production of acute inflammatory proteins, thereby causing the problem of difficulty in detecting infections at an early stage.

In addition, occurrence of tuberculosis has recently been of particular concern, although etanercept appears to be rarely associated with tuberculosis as compared with infliximab.5,6 However, caution should be exercised when etanercept is used in Japan, where tuberculosis frequently occurs,7 because BCG vaccinations in Japan preclude the use of the tuberculin skin test for screening at the start of drug treatment, and there are not a few patients with drugresistant Mycobacterium tuberculosis.8,9

Although the occurrence of malignancies was the most serious among possible complications, the incidence in the more than 1100 patients was not significantly different from the expected incidence in the general population. Also, patients with active RA have been shown to have a slightly higher incidence of malignant lymphoma. In March 2003, the FDA reported that the standardized incidence ratio (SIR) for malignant lymphoma ranged from 2.3 to 3.5 in patients receiving etanercept with no statistically significant difference.10

Because etanercept is known to exacerbate congestive heart failure, caution should be made when etanercept is administered to patients with heart failure. Initially, clinical trials were conducted with infliximab or etanercept as a therapeutic agent for congestive heart failure because TNF-α was believed to be involved in the pathophysiology of congestive heart failure. However, individual clinical trials showed treatment failures and even worsening cases of congestive heart failure, leading to termination of these trials.11

In addition, rare cases of pancytopenia have been reported. Although demyelinating diseases in the central nervous system have also been reported, a causal relationship to the treatment remains uncertain. In some patients with multiple sclerosis, an increase in disease activity has been found after the treatment.12 A recent report showed that etanercept treatment in early RA patients was well tolerated for up to 5 years.13

In Japan, 147 patients who were refractory to conventional DMARDs were enrolled in phase II clinical study. Patients were randomly divided into three groups, i.e., placebo group, 10mg twice-weekly group, and 25mg twice-weekly group, and treated for 12 weeks. Consequently, both the 10mg group and 25mg group yielded an almost identical ACR20 response, significantly better than the placebo group (64.0%, 65.3% vs. 6.3%, respectively). This trend was similar in both ACR50 and ACR70 response. There was no significant difference observed in severe adverse effects between the etanercept and placebo groups.

Treatment guidelines for the use of etanercept (Table 1)14

Table 1.

Treatment guidelines for the use of etanercept

A.	Inclusion criteria
Patients with active rheumatoid arthritis still presenting the following despite the use of one or more MHLW recommendation-level-ADMARDsa (methotrexate, bucillamine, or sulfasalazine) at a normal dose for more than 3 months:
	(1)	Tender joints ≥6
	(2)	Swollen joints ≥6
	(3)	ESR ≥28mm/h or CRP ≥2.0 mg/dl
Also, the patients must meet the following as having low risk for opportunistic infections:
	(1)	WBC ≥4000/mm3
	(2)	Peripheral blood lymphocytes ≥1000/mm3
	(3)	Serum β-d-glucan: negative
B.	Usage
The dose of etanercept is 10–25 mg administered twice weekly as a subcutaneous injection. A patient can self-inject etanercept only after the ability to self-inject is carefully assessed and appropriate training is provided by a health professional.
C.	Contraindication
	1.	Ongoing infection
	2.	Past history of serious infections in the last 6 months
	3.	Abnormal shadows on chest radiographs suggestive of old pulmonary tuberculosis (TB) or tuberculosis pleuritis
	4.	History of extra pulmonary TB or Pneumocystis carinii pneumonia
	5.	Congestive heart failure
	6.	Malignancy or demyelinating disease
D.	Caution
	1.	From the point of view of screening for infection (especially TB and opportunistic infections) as well as prevention of side effects, etanercept is recommended for clinical use at medical institutes where:
		(1)	Chest X-rays can be obtained on the same day, and the X-ray can be interpreted by a pulmonologist, TB specialist, or radiologist
		(2)	Opportunistic infections can be treated
	2.	Comprehensive TB screening should be conducted including an in-depth patient history, chest radiographs (chest CT whenever possible) and a PPD skin test. In patients with suspected TB, based on medical history, abnormal shadows on chest radiographs suggestive of old pulmonary TB, or with a PPD skin test positive (as evidenced by redness of at least 20 mm in diameter or the presence of induration), the treatment with etanercept may be considered in addition to anti-tuberculosis drugs only if the potential benefits outweigh the potential risks.

MHLW, Ministry of Health, Labor and Welfare; DMARD, disease-modifying antirheumatic drug; ESR, erythrocyte sedimentation rate; CRP, C-reactive protein; WBC, white blood cells; TB, tuberculosis; CT, computed tomography; PPD, purified protein derivative

^a Cited in the Diagnostic Manual and Evidence-based Treatment Guidelines

For the safe use of etanercept in Japan, which produces such high efficacy and potential adverse events, the internal medicine rheumatology study group of the Ministry of Health, Labor and Welfare, Japan (led by N.M., T.T., and K.E.) has developed the guidelines for treatment with etanercept, which provide indications, contraindications, and tuberculosis risk assessment, which was based on the guidelines for the use of infliximab for RA patients in Japan9 (Fig. 1). The guidelines were approved by the board of directors of Japan College of Rheumatology.

Fig. 1.

Tuberculosis risk evaluation chart of the use of anti-TNF therapy. TNF, tumor necrosis factor; INH, isoniazid; PMS, postmarketing survery

Etanercept is indicated in patients with active RA at or above a certain level. Specifically, etanercept may be used in patients who have inadequately been controlled despite treatment of at least 3 months with the usual doses of one of the DMARDs (methotrexate, bucillamine, or sulfasalazine), which are rated as “recommendation A level” in the Diagnostic Manual and Evidence-based Treatment Guidelines15 developed by the study group of the Ministry of Health, Labor and Welfare. Leflunomide, another DMARD rated as recommendation A, is not included in the present guidelines because of the adverse event of serious interstitial pneumonia observed in Japan.16 Inadequate response to previous treatment is defined by the presence of at least six tender joints and swollen joints and either C-reactive protein levels of at least 2.0 mg/dl or erythrocyte sedimentation rate (ESR) of at least 28mm/h.

To avoid potential opportunistic infections, patients should have a peripheral leukocyte count of 4000/mm³ or more, peripheral lymphocyte count of 1000/mm³ or more, and a negative test for blood β-d-glucan. These criteria are based on the findings that cellular immunity plays an important role in opportunistic infections caused by Mycobacterium tuberculosis or fungi such as Pneumocystis jiroveci, and that these infections are likely to occur in patients with decreased peripheral lymphocyte counts.17 A test for blood β-d-glucan has been included because β-d-glucan, a component of fungi, may be diagnostic of fungal infections, especially infections with Pneumocystis jiroveci.

The recommended dosage and administration of etanercept in Japan is 10–25 mg given once daily and twice weekly as a subcutaneous injection. In this aspect, onceweekly administration of 50mg etanercept in patients with active RA patients has been approved in the United States, and this dosing regimen was shown to be equivalent to 25 mg etanercept twice weekly in terms of safety, efficacy, and pharmacokinetics.18 Patients will switch to self-injection after they are assessed as capable of conducting self-injections and receive adequate instructions. Etanercept may be used as monotherapy as the drug was administered so in clinical trials in Japan. In Europe and the United States, however, etanercept in combination with MTX has been demonstrated to provide greater efficacy in TEMPO.4 Thus, the combination of etanercept with MTX should be considered in patients with highly active disease in Japan.

Etanercept is contraindicated in patients with active infections or a history of serious infections within the previous 6 months. In addition, careful assessment of the risk of tuberculosis should be made. Specifically, the following three examinations should be performed before treatment initiation: interview with respect to family and past history of tuberculosis, chest radiography, and purified protein derivative (PPD) skin test (Fig. 1). Chest radiographs should preferably be interpreted by a specialist in pulmonology, tuberculosis, or radiology. When abnormalities are suspected on chest radiography, computed tomography of the chest should be performed. Etanercept is contraindicated in patients with abnormalities in chest radiographs such as linear opacities, calcification ≥5mm, and pleural thickening suggesting old pulmonary tuberculosis, and individuals infected with pulmonary or extrapulmonary tuberculosis. However, treatment with etanercept may be considered with antituberculous agents only if the potential benefits outweigh the potential risks. In patients with a positive PPD skin test (as evidenced by erythema of at least 20mm in diameter or the presence of induration) or opacities suggesting old pulmonary tuberculosis on chest radiographs, treatment with isoniazid 0.3 g/day should be initiated at least 1 month prior to administration of etanercept and continued for the subsequent 9 months. However, no definite guidelines are available that address how to deal with isoniazid-induced hepatic impairment and isoniazid-resistant Mycobacterium tuberculosis, as well as how long isoniazid treatment should be given. Etanercept is also contraindicated in patients with previous Pneumocystis jiroveci pneumonia, congestive heart failure, malignancies, or demyelinating disease.

To sum up, in this article we focused on the guidelines for the use of etanercept that have been introduced in Japan since spring 2005. In Japan, because only about 100 patients received etanercept in clinical trials, it remains uncertain whether etanercept yields clinical benefit and adverse events with a similar frequency as observed in Europe and the United States. Nonetheless, we will conduct an all-cases postmarketing surveillance using the above-mentioned treatment guidelines, review the results, and revise the guidelines as needed.