|Year : 2017 | Volume
| Issue : 3 | Page : 139-145
Clinical experience with two etanercept biosimilars in Indian patients with spondyloarthritis
Ashok Kumar, Anshul Goel, Mehul Lapsiwala, Mohit Goyal, Gaurav Dembla
Department of Rheumatology, Fortis Flt. Lt. Rajan Dhall Hospital, New Delhi, India
|Date of Web Publication||27-Jul-2017|
Department of Rheumatology, Fortis Flt. Lt. Rajan Dhall Hospital, Vasant Kunj, New Delhi - 110 070
Source of Support: None, Conflict of Interest: None
Background: Antitumor necrosis factor (TNF) drugs are highly efficacious in spondyloarthritis (SpA). We present retrospective analysis of our experience with 2 etanercept biosimilars (Etacept and Intacept).
Methods: Clinical record of patients with axial and/or peripheral SpA (Assessment of SpA International Society [ASAS] criteria) registered during April 2013–September 2016 was retrieved. Those with active disease (Bath Ankylosing Spondylitis Disease Activity Index [BASDAI] >4), despite 1-month trial of two non-steroidal anti-inflammatory drugs (NSAIDs) (axial) and/or 3-month trial of disease modifying anti-rheumatic drugs (peripheral), received anti-TNF therapy. Etanercept biosimilar (50 mg) was administered weekly for the first 12 weeks. Patients achieving “major improvement” after 12 weeks (Ankylosing Spondylitis Disease Activity Score [ASDAS] reduction by >2 points) received the dose every 2 weeks subsequently. BASDAI, Bath Ankylosing Spondylitis Functional Index, and ASDAS and NSAID index were noted at baseline, 12, and 24 weeks. For Etacept, week 52 and 104 data were also available. Primary endpoint was BASDAI <4 at 12 weeks.
Results: Males constituted the majority (76%) and mean ASDAS was 4.7. In patients receiving Etacept, BASDAI <4 and major improvement were achieved by 12 weeks in 77% (42/54) and 61% (33/54) patients, respectively. Forty-three patients had completed 52 weeks and 27 patients had completed 104 weeks of treatment. Among 27 patients completing 104 weeks, secondary end points: ASAS 20, 40, and ASAS-partial remission status were achieved by 89%, 67%, and 41%, respectively. Intacept results were available up to 24 weeks and were comparable to those of Etacept. Injection site reactions followed by upper respiratory tract infections were the most common adverse reactions. One patient developed tuberculous pleural effusion.
Conclusion: Etanercept biosimilar therapy was found efficacious and safe.
Keywords: Antitumor necrosis factor, biological, biosimilar, etanercept, spondyloarthritis
|How to cite this article:|
Kumar A, Goel A, Lapsiwala M, Goyal M, Dembla G. Clinical experience with two etanercept biosimilars in Indian patients with spondyloarthritis. Indian J Rheumatol 2017;12:139-45
|How to cite this URL:|
Kumar A, Goel A, Lapsiwala M, Goyal M, Dembla G. Clinical experience with two etanercept biosimilars in Indian patients with spondyloarthritis. Indian J Rheumatol [serial online] 2017 [cited 2020 Jul 7];12:139-45. Available from: http://www.indianjrheumatol.com/text.asp?2017/12/3/139/211696
| Introduction|| |
Spondyloarthritis (SpA) is an important category of chronic inflammatory joint disease. The socioeconomic burden of SpA can be considerable, due to work disabilities, use of healthcare resources, and sometimes to the patient's depressed mood or low social functioning.,,,,, The first-line therapy for the axial SpA consists of nonsteroidal anti-inflammatory drugs (NSAIDs) and regular exercise, but they are not effective in many cases. Disease modifying anti-rheumatic drugs (DMARDs) such as sulfasalazine, methotrexate, or leflunomide are recommended for treating peripheral arthritis or extra-articular features. However, in patients refractory to above measures, antitumor necrosis factor (TNF) drug is a reliable option. The Assessment of SpA International Society (ASAS) recommends use of anti-TNF in patients diagnosed with AS or SpA if they have active disease and have not improved with conventional treatment (NSAIDs and DMARDs). All four TNF-alpha blockers currently available in India for the treatment of AS (infliximab, adalimumab, etanercept, and golimumab) demonstrated similar high efficacy in patients who did not respond to previous NSAIDs therapy.,,, As patents for innovator anti-TNF drugs expire, pharmaceutical manufacturers have developed copies of innovator molecules at considerably lower production cost. These have also been called “biosimilars” by NICE. Biosimilar is a biological medicine which has been shown not to have any clinically meaningful differences from the originator biological drug in terms of quality, safety, and efficacy.“ We report our clinical experience with two etanercept biosimilars in patients with SpA. These local biosimilars are approved by the Drug Controller General of India. We used “Etacept” (introduced in the Indian market with effect from April 2013) and “Intacept” (introduced with effect from April 2015). We also tried to examine if the efficacy of etanercept biosimilars was sustained after reducing the dosing frequency.
| Methods|| |
This was a retrospective chart review in which we retrieved the clinic records of patients who fulfilled the following inclusion criteria;
- Patients with axial and/or peripheral SpA (according to ASAS criteria) attending our rheumatology clinic during April 2013–September 2016 and
- Those with active disease (>4 Bath Ankylosing Spondylitis Disease Activity Index [BASDAI]) despite a 1-month trial of at least two NSAIDs (for axial symptoms only) with or without 3-month trial of DMARDs (for peripheral joint symptoms).
Following patients were excluded;
- Patients who did not complete at least 12 weeks of etanercept biosimilar therapy or
- Patients with active tuberculosis, current or past history of hepatitis B, hepatitis C or human immunodeficiency virus, demyelinating disease, alcohol abuse, psychiatric illness, symptoms of severe and progressive or uncontrolled renal, hepatic, hematologic, gastrointestinal, endocrine, pulmonary, cardiac, neurological, or cerebral disease, congestive heart failure, history of any form of cancer within the past 10 years, history of serious infection requiring hospitalization in the past 6 months, and history of any surgery in the past 12 weeks. Women with pregnancy or who were breastfeeding were also excluded from the study.
Screening for latent tuberculosis (TB) included chest X-ray, interferon gamma release assay (“Quantiferon-TB-Gold“), and Mantoux test (1 TU). In addition, hepatitis B surface antigen and anti-hepatitis C virus status were also obtained before starting anti-TNF therapy. Patients with latent TB received rifampicin and isoniazid for 6 months, started simultaneously with anti-TNF therapy. Baseline assessment parameters included BASDAI, Bath Ankylosing Spondylitis Functional Index (BASFI), Ankylosing Spondylitis Disease Activity Score (ASDAS), and NSAID consumption index.,, These were repeated at 12 weeks, 24 weeks, 52 weeks, and 104 weeks after starting the treatment with Etacept and at 12 weeks and 24 weeks after starting treatment with Intacept. Other parameters assessed at above-mentioned time points included ASAS-20 (Assessment of SpA International Society), ASAS-40, and ASAS-partial remission (ASAS-PR)., The primary endpoint was achievement of BASDAI <4 and secondary endpoints were achievement of ASAS 20, ASAS 40, and ASAS-PR responses. Patients were also advised physiotherapy in the form of spinal extension exercises, deep breathing exercises, and regular aerobic exercises such as brisk walk, cycling, and swimming. Etanercept biosimilar 50 mg was administered subcutaneously weekly for first 12 weeks. In the first 2 years starting from April 2013, we used only Etacept while afterward most new patients received Intacept when the latter became available. Patients initially treated with Etacept continued the same drug except when discontinuation was necessitated by inefficacy or adverse effect. Same was applicable in case of Intacept. Patients achieving “major improvement” after 12 weeks (as defined by ASAS i.e., reduction of ASDAS by >2 points) received same biosimilar every 2 weeks subsequently. The patients who failed to achieve “major improvement” at the end of 12 weeks were continued on weekly dose of prescribed biosimilar. They were then assessed at the end of 24 weeks for the achievement of “major improvement” and if achieved, were switched to once every 2 weeks dosages. In case of worsening of symptoms, patients were reverted to weekly regimen. Patients with lack of any response at 12 weeks discontinued the drug. Adverse effects of treatment were carefully noted. Patients who discontinued following up with rheumatology clinic were contacted telephonically and their missing data were received through E-mail or on next personal visit at clinic.
The study protocol was approved by the Ethics Committee of our institution.
| Results|| |
[Figure 1]a and [Figure 1]b give the outline of patients considered eligible for anti-TNF therapy. A total of 82 patients were started on etanercept biosimilar. Five patients had to be excluded due to discontinuation of treatment during first 12 weeks (3 had an adverse reaction and 2 decided to drop out because of fear of adverse effects). Thus, 77 patients continued the treatment (Etacept 54, Intacept 23). [Table 1] gives the baseline demographic characteristics of these patients.
|Figure 1: (a) Outline of patient response in Etacept group. (b) Outline of patient response in Intacept group. *Depending on physician's evaluation and patient reported global assessment|
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Both etanercept biosimilars provided excellent symptom relief in axial symptoms and in patients with psoriatic arthropathy. Response in peripheral arthritis and entheseal symptoms remained moderate.
Details of clinical response are shown in [Figure 1]a. It is noteworthy that progressive improvement in all endpoints occurred over time with Etacept. [Figure 2] gives the graphical presentation of the trend of improvement. The primary endpoint was achieved by 77% (42/54) patients. [Table 2] gives serial outcomes, including achievement of secondary endpoints at various time intervals. After commencing Etacept, 10 out of 54 patients did not require any NSAID in first 3 months of therapy. Overall reduction of NSAID index can be observed in [Table 2]. As many as 43 patients had completed 52 weeks and 27 patients had completed 104 weeks. Twelve patients were able to maintain major improvement status on once a month dose of Etacept. Seven out of ten patients were able to discontinue oral corticosteroids. Three patients, who were unable to taper off steroids, had primary failure of Etacept. One patient had axial SpA with inflammatory bowel disease (IBD), in whom IBD was asymptomatic at the time of starting Etacept. His axial symptoms responded well with treatment without any recurrence of IBD-related symptoms during 2 years of follow-up. There were three patients who had only partial improvement at the end of 12 weeks. Although their BASDAI did not fall below four, their NSAID consumption index had dropped substantially. They were reluctant to discontinue the biosimilar for lack of a better alternative. Hence, we kept them in follow-up while continuing weekly dose of Etacept. At the end of 6 months, one of these three patients achieved “major improvement,” so he was switched to Etacept once every 2 weeks dosage. He remained well on the same dosage at the end of 1-year follow-up.
|Figure 2: Graphical presentation of serial outcomes. (a) Trend of assessment of spondyloarthritis international society 20, assessment of spondyloarthritis international society 40, and assessment of spondyloarthritis international society partial remission response achievement. (b) Bath Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Disease Activity Index, and nonsteroidal anti-inflammatory drug index trend for Etacept. (c) Bath Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Disease Activity Index, and nonsteroidal anti-inflammatory drug index trend for Intacept|
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[Figure 1]b shows details of clinical response in Intacept group. The primary endpoint was achieved by 61% (14/23) patients. [Table 2] gives serial outcomes of various parameters over 24 weeks. Same is depicted in graphical manner in [Figure 2]. After starting Intacept, as many as eight patients were able to discontinue NSAIDs completely. Four out of five patients were able to taper off oral corticosteroids. One patient, who could not discontinue steroids, had primary failure of Intacept. There were two patients who had only partial improvement at the end of 12 weeks. Although their BASDAI did not fall below 4, they wished to continue the biosimilar for lack of a better alternative. Hence, they were kept in follow-up, while continuing weekly dose of Intacept. Although only short-term data were available for Intacept, the improvement trend appeared similar to that of Etacept.
Overall, injection site reactions were the most common adverse reactions followed by upper respiratory tract infections. In Etacept group, we noted injection site reactions (n = 9), upper respiratory tract infections (n = 4), skin and subcutaneous tissue infections (n = 2), recurrence of acute anterior uveitis (n = 1), episode of Vitritis (n = 1), reactivation of TB (n = 1), weight gain (n = 1), diarrhea (n = 1), and headache (n = 1). Four patients had to discontinue Etacept due to adverse events. In Intacept group, injection site reactions (n = 2), upper respiratory tract infections (n = 1), weight gain (n = 1), polycythemia (n = 1), hair fall (n = 1), and headache (n = 1) were observed. Two patients had to discontinue Intacept due to treatment emergent adverse events.
History of acute anterior uveitis was present in 11 patients in Etacept group and five patients in Intacept group, of whom only 1 had recurrence of uveitis (4 months after starting Etacept). Etacept was discontinued after recurrence of uveitis. His uveitis recovered completely with a short course of topical steroid therapy. One patient developed tuberculous pleural effusion after 31 months of Etacept therapy. His screening for latent TB was positive (Mantoux test > 20 mm) and he had received rifampicin and isoniazid as part of treatment of latent TB infection. Etacept was discontinued and full course of antitubercular therapy was administered, following which he completely recovered from tuberculosis.
| Discussion|| |
This retrospective study in patients with active SpA shows that treatment with etanercept biosimilars is both efficacious and safe. Progressive improvement in terms of disease activity was observed over time. Most patients remained in a state of low disease activity during the study period. In addition, there was a significant improvement in BASFI score implying that a proportion of the functional loss in AS patients is reversible.
Murphy et al. showed that the efficacy of etanercept could be sustained even with reduced dosing frequency once a stable state of improvement was achieved. Encouraged by this observation coupled with financial constraints in the Indian setting, we reduced the frequency of Etacept injections to once in 2 weeks after the first 12 weeks of treatment. The efficacy remained uncompromised in majority of patients during the entire follow-up. Intacept showed the same trend though only limited data are available till now. An open-label observational study by Brandt et al. on etanercept innovator product with once a week dosing reported ASAS 20 and ASAS 40 response at 54 weeks in 72.1% and 63.5% patients, respectively. They also reported mean BASDAI value of 2.8 ± 2.3 at week 54. In our retrospective analysis, we obtained ASAS 20 and ASAS 40 response at 52 weeks in 81% and 56% patients, respectively. Mean BASDAI value at this time point was 2.5 ± 0.9. These results are comparable and their significance is increased by the fact that our patients received lower cumulative doses of the drug. The strategy of reducing the dosage frequency without loss of efficacy has implications on the cost of treatment as well. This is of special relevance in resource-constrained countries such as India, where most patients are neither covered by medical insurance nor supported by government or employer.
Overall, adverse event profile did not differ significantly from what is previously reported for the innovator product. India has a relatively high prevalence of active and latent tuberculosis as compared to developed countries. Reduced dosing frequency may also bring down the risk of reactivation of latent tuberculosis in our patients. This has already been noted in the case of infliximab treatment of spondyloarthropathy. The lone patient who developed tuberculous pleural effusion after 31 months of Etacept therapy in the present study had already received 6 months course of rifampicin and isoniazid for his latent TB at the start of anti-TNF therapy. The reason for TB in his case may be a new exposure to TB. Good response to first-line antitubercular drugs rules out any possibility of drug-resistant TB. This case also demonstrates the ever persisting possibility of developing TB in patients receiving anti-TNF drugs in high TB burden countries despite initial treatment of latent TB.
Most experts advise that antitubercular therapy (ATT) should be started at least 1 month before the commencement of anti-TNF therapy if latent TB is present. In the present study, we started ATT and etanercept biosimilar at the same time without any adverse consequence. This is consistent with an earlier observation that etanercept does not cause reactivation tuberculosis in the first 6 months of therapy.
Although the prevalence of latent TB infection identified by standard Mantoux positivity in India is 44%, we found Mantoux positivity rate of 27% only in patients with SpA in this study. This may be due to the phenomenon of anergy in rheumatic diseases. It is interesting to note that no Mantoux negative patient developed reactivation TB. Probably, the interferon gamma release assay adequately compensated for the diagnostic gap resulting from tuberculin anergy.
Acute anterior uveitis as a potential side effect of etanercept which is already well documented in literature.,,, In this retrospective report, we had prescribed Etacept to 11 patients and Intacept to five patients, who already had a history of acute anterior uveitis. Discontinuation of Etacept was required in one patient, who developed unilateral acute anterior uveitis after first 4 months of treatment. He was receiving Etacept once every week. All other patients receiving Etacept or Intacept could continue treatment without any further episodes of uveitis. No patient had developed a new-onset acute anterior uveitis while on etanercept biosimilar therapy. We hypothesize that reducing the dosage frequency might have impact on reducing the incidence of attacks of uveitis.
Limitations of this study include its retrospective design, absence of control group to compare the results, 104-week follow-up only on 27 patients in Etacept group, and small sample size of Intacept group (as Intacept was introduced in Indian market much later). We did not do a formal cost-benefit analysis to obtain an estimate of the economic impact of biosimilar therapy. Further studies addressing these limitations are necessary. Despite these limitations, overall data show encouraging results on efficacy and safety of both the biosimilars.
The etanercept biosimilars were generally well tolerated in this study, with no unexpected safety issues in either group. The overall efficacy profile was comparable to that of the innovator product. The strategy of reduced dosing frequency following initial 12 weeks of standard regimen did not result in any loss of efficacy.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]