Psoriasis is a chronic, immune-mediated, inflammatory disease with a high prevalence in the general population (2%) and an important impact on the quality of life [1].

Treatment adherence to anti-tumor necrosis factor-alpha (anti-TNF-α) agents is an overall marker of treatment success, and it depends on multiple factors, such as efficacy, safety profile, patient satisfaction, and physician’s confidence with the drug used. Clinical trials and registries indicated that the overall efficacy of anti-TNF-α decreases over time leading to a progressive loss of patient adherence to treatment. Studies have revealed that the major reason for treatment discontinuation is the loss of efficacy, followed by adverse events [2] [3] [4] [5] [6].

The soluble tumor necrosis factor receptor etanercept is approved by the FDA for the treatment of moderate to severe plaque psoriasis [7].

In real-world experience, patients and practicing dermatologists may opt to use etanercept intermittently for various reasons, including interruptions in insurance coverage or preparation for surgery. A recent study demonstrated control of psoriasis symptoms after discontinuation and re-treatment with etanercept [8].

In the present case report, we are describing a 39-year-old adult male with a long-standing history of chronic plaque psoriasis who improved and sustained efficacy on just loading injection of etanercept therapy for 36 weeks followed-up. The consent form was taken from the patient about the publication of his condition.

A 39-year-old adult male patient presented to our clinic with long-standing, severe plaque psoriasis for 15 years duration without joint involvement. For several years, he received multiple appropriate topical therapies (e.g. tar, topical corticosteroids, and vitamin D analogs), and narrowband UVB phototherapy but remained refractory to treatment. He was initially treated with 15 mg per week oral methotrexate, which resulted in significant improvement.

However, abnormal findings in liver functions were noted, unfortunately, leading to discontinuation.

On examination, the patient had diffuse erythematous, inflammatory plaques covered with adherent white silvery scales involving 25% of the body surface area (BSA) and psoriasis area and severity index (PASI) score of 13. Biological therapy was recommended and induction treatment with etanercept was initiated with 50 mg twice weekly for the first 12 weeks. On follow-up, after 8 weeks disease was stabilized, with mild erythema involving 1% of BSA, a PASI score of 1.3.

Due to his work circumstances, he did not show up to his scheduled follow-up after the finished induction dose. However, he came after 36 weeks from the first induction dose of etanercept when the disease relapsed involving mostly the lower legs and on examination, PASI score was 7.2 and BSA 12%. According to the patient, this relapse started last week (Figure 1).

Thus, full patient screening was done for safety and for discovering any hidden disorder including complete blood count, erythema sediment rate, C-reactive protein, lactate dehydrogenase, liver function test, lipid profile, electrolyte panel, QuantiFERON-TB GOLD blood test, chest x-ray and resulted with no risk factors could appear. Re-treatment with the same induction dose of etanercept was given and instructs the patient coming back for follow up after one month to assess the improvement, but he came again after 36 weeks from the first injection showed sustained efficacy and no side effect and on examination, PASI score was 1.3 and BSA 1% (Figure 2). The recommendation is given to the patient to follow up monthly for any signs of relapse and continuing on just topical moisturization.

In some studies that compare continuous and interrupted etanercept therapy, both the results were effective and well-tolerated in patients with psoriasis, with greater improvements observed in the continuous arm at week 24 and most patients regained their response after re-initiation of etanercept [9]. While in other reports, treatment survival was constantly high in patients going intermittent regimen with optimal clinical success and adherence [6].

Psoriasis is commonly a chronic disease that requires continuous treatment. However, for some patients, it is characterized by more extended periods of remission and intermittent relapse. In the clinical setting, interruption of therapy may occur for reasons such as disease remission, discontinuation of insurance coverage, cost-effectiveness, concurrent disease, intercurrent illness, or preparation for surgery. The risks involved in stopping and restarting therapy are relapse, rebound, or tachyphylaxis and inability to regain efficacy [10]. In our case report, the reason for restart medication is the relapse of disease after a prolonged remission period.

Etanercept was initially approved in European countries for patients with psoriasis only with intermittent schedules up to 24 weeks, with re-treatment after treatment interruption in case of disease recurrence [6]. In our report, the intermittent therapy is prolonged up to 36 weeks and the disease was controlled with sustained efficacy and without any serious infection or adverse effect observed.

This study added to other studies that discuss continuous and intermittent etanercept therapy [6] [9].

In conclusion, intermittent etanercept treatment of the patient with moderate to severe plaque psoriasis is safe, well-tolerated, and efficacious after induction dose for 36 weeks without adverse effect.

However further studies are required involving more patients, to assess the response to these prolonged remission periods.

The authors declare no conflicts of interest regarding the publication of this paper.

Abdulwahhab, W.S. and Mehair, A.S. (2021) Interrupted Etanercept Therapy: A New Case Report. Journal of Cosmetics, Dermatological Sciences and Applications, 11, 71-75. https://doi.org/10.4236/jcdsa.2021.112007