Abstract:Since targeted biologic treatments have been introduced for the treatment of plaque-type psoriasis and psoriatic arthritis, switching between different medications has become necessary in selected patients, particularly after treatment failures. To evaluate the efficacy and safety of etanercept treatment in adult patients with psoriasis after failure to respond to other previous therapies. In particular, the differences in efficacy profiles after switching from traditional (cyclosporine [ciclosporin], methotre… Show more
“…The clinical benefits of etanercept are well established with regard to peripheral joint disease and skin symptoms 17,20,21,22,23,29 . Thus, in pivotal trials, 12-week treatment with etanercept led to significant increases, relative to placebo, in the proportion of patients with PsA achieving the PsARC and PASI 75-level skin clearance.…”
Section: Discussionmentioning
confidence: 99%
“…Etanercept discontinuation because of safety concerns has occurred rarely 19,30,37 or not at all 29,36 in available studies, although British patient registry data suggested that about 3% of patients discontinued etanercept per year, citing AE 38 .…”
Section: Discussionmentioning
confidence: 99%
“…Established clinical benefits of etanercept treatment in PsA include amelioration of skin disease 19,21,22,28,29 , reduction in joint pain and swelling 21 , and prevention of radiographic progression 17,19 . In parallel with these responses, some studies have also established significant benefits in health-related quality of life 17,30,31 .…”
Objective.To describe the longterm effectiveness and safety of etanercept in Canadian patients with psoriatic arthritis (PsA), treated over 24 months in clinical practice.Methods.Patients with active PsA (≥ 3 tender and ≥ 3 swollen joints) were recruited from 22 centers. Etanercept was administered at 50 mg/week subcutaneously. In addition to clinical assessment of skin and joint disease, conducted at baseline and at Months 6, 12, 18, and 24, regular patient interviews were conducted by telephone. Patient responses related to health status, disability, and work productivity were scored using the patient global assessment tool, the Health Assessment Questionnaire (HAQ), the Health and Labour Questionnaire (HLQ), and the Fatigue Severity Scale.Results.Out of 110 patients, 71 (65%) maintained etanercept treatment through the end of our study. All clinical measures of disease severity, including joint tenderness/pain, joint swelling, and Psoriasis Area and Severity Index score, improved significantly between baseline and Month 6 of etanercept treatment and remained constant thereafter. By the end of our study, 79% of patients achieved a Psoriatic Arthritis Response Criteria response, and 56% of patients achieved a 0.5-point improvement on HAQ, indicating clinically significant improvement in disability; 14% of patients finished our study free of disability (HAQ = 0). Patients’ work productivity and fatigue improved significantly in parallel with these clinical and functional improvements.Conclusion.Continuous treatment with etanercept over 2 years in a clinical setting improved clinical symptoms of PsA while reducing fatigue, improving work productivity, and ameliorating or eliminating disability.
“…The clinical benefits of etanercept are well established with regard to peripheral joint disease and skin symptoms 17,20,21,22,23,29 . Thus, in pivotal trials, 12-week treatment with etanercept led to significant increases, relative to placebo, in the proportion of patients with PsA achieving the PsARC and PASI 75-level skin clearance.…”
Section: Discussionmentioning
confidence: 99%
“…Etanercept discontinuation because of safety concerns has occurred rarely 19,30,37 or not at all 29,36 in available studies, although British patient registry data suggested that about 3% of patients discontinued etanercept per year, citing AE 38 .…”
Section: Discussionmentioning
confidence: 99%
“…Established clinical benefits of etanercept treatment in PsA include amelioration of skin disease 19,21,22,28,29 , reduction in joint pain and swelling 21 , and prevention of radiographic progression 17,19 . In parallel with these responses, some studies have also established significant benefits in health-related quality of life 17,30,31 .…”
Objective.To describe the longterm effectiveness and safety of etanercept in Canadian patients with psoriatic arthritis (PsA), treated over 24 months in clinical practice.Methods.Patients with active PsA (≥ 3 tender and ≥ 3 swollen joints) were recruited from 22 centers. Etanercept was administered at 50 mg/week subcutaneously. In addition to clinical assessment of skin and joint disease, conducted at baseline and at Months 6, 12, 18, and 24, regular patient interviews were conducted by telephone. Patient responses related to health status, disability, and work productivity were scored using the patient global assessment tool, the Health Assessment Questionnaire (HAQ), the Health and Labour Questionnaire (HLQ), and the Fatigue Severity Scale.Results.Out of 110 patients, 71 (65%) maintained etanercept treatment through the end of our study. All clinical measures of disease severity, including joint tenderness/pain, joint swelling, and Psoriasis Area and Severity Index score, improved significantly between baseline and Month 6 of etanercept treatment and remained constant thereafter. By the end of our study, 79% of patients achieved a Psoriatic Arthritis Response Criteria response, and 56% of patients achieved a 0.5-point improvement on HAQ, indicating clinically significant improvement in disability; 14% of patients finished our study free of disability (HAQ = 0). Patients’ work productivity and fatigue improved significantly in parallel with these clinical and functional improvements.Conclusion.Continuous treatment with etanercept over 2 years in a clinical setting improved clinical symptoms of PsA while reducing fatigue, improving work productivity, and ameliorating or eliminating disability.
“…Similarly, in patient 8, switching to etanercept after previous TNF-antagonist failure was not successful. Although etanercept may represent an effective and well-tolerated alternative treatment for psoriasis patients who have failed to respond to other therapies (traditional or biologic), it has been reported that etanercept was more effective in biologic naive patients [20]. However, the rate of response to a second TNF antagonist is usually inferior to that of the first [16].…”
An association among the occurrence of antidrug antibodies (ADAs), diminished trough serum drug levels (TSDLs) and non-response or loss of response has been described for several tumor necrosis factor alpha (TNF) blocking agents in a variety of diseases, including psoriasis. In a series of ten psoriasis patients with primary or secondary failure, or adverse reactions during anti-TNF therapy, we measured ADAs and TSDLs in patient serum using radioimmunoassay and ELISA, respectively. By proposing a treatment algorithm derived from research in this field, we show that measuring ADAs and TSDLs in psoriasis patients provides a more structured approach to clinical decision making for psoriasis patients who fail anti-TNF therapy.
“…Data pertaining to patients with psoriasis who switch from one TNF-a antagonist to another, however, have been limited generally to small studies. [14][15][16][17][18][19][20] In the current study, the efficacy of this alternative treatment paradigm was evaluated by assessing clinical response in patients with plaque psoriasis who switch to infliximab after having an inadequate response (IR) to etanercept.…”
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