Abstract:IntroductionPharmacoeconomic studies examining the cost-effectiveness of biological agents to treat moderate-to-severe psoriasis in real-life clinical practice are scarce. The aim of this study was to assess the efficiency, in terms of incremental cost-effectiveness, of etanercept and adalimumab in a real clinical setting.MethodsDirect and indirect costs were assessed from a Spanish societal perspective in a historical hospital cohort of patients with moderate-to-severe psoriasis attending a tertiary referral … Show more
“…Our study clearly demonstrates the difference between patients that do continuous therapy versus intermittent therapy, with differences of close to E2000 and E7300 in the first and the second year between both regimens. However, the use of tailored treatment strategies such as the induction dose of 50 mg/ weekly allow us to achieve costs lower than those of other hospitals in our setting (21). Etanercept, together with adalimumab, and by virtue of their posology, permits greater therapeutic flexibility, leading to lower costs, as asserted by Puig in his study published in 2013, and even without significant differences in terms of efficacy between both drugs, as substantiated by Ruano (21).…”
We present our experience in regular clinical practice with etanercept, showing it to be an effective, safe, and versatile drug that permits patient-tailored treatment, delivering a frankly satisfactory control of our psoriasis patients.
“…Our study clearly demonstrates the difference between patients that do continuous therapy versus intermittent therapy, with differences of close to E2000 and E7300 in the first and the second year between both regimens. However, the use of tailored treatment strategies such as the induction dose of 50 mg/ weekly allow us to achieve costs lower than those of other hospitals in our setting (21). Etanercept, together with adalimumab, and by virtue of their posology, permits greater therapeutic flexibility, leading to lower costs, as asserted by Puig in his study published in 2013, and even without significant differences in terms of efficacy between both drugs, as substantiated by Ruano (21).…”
We present our experience in regular clinical practice with etanercept, showing it to be an effective, safe, and versatile drug that permits patient-tailored treatment, delivering a frankly satisfactory control of our psoriasis patients.
Biological therapy for moderate-to-severe psoriasis is highly effective but cost-intensive. This systematic review aimed at analyzing evidence on the cost-effectiveness of biological treatment of moderate-to-severe psoriasis. A literature search was conducted until 30/06/2017 in PubMed, Cochrane Library, LILACS, and EconLit. The quality of identified studies was assessed with the checklist by the Centre for Reviews and Dissemination guidance. Out of 482 records, 53 publications were eligible for inclusion. Half of the studies met between 20 and 25 of the quality checklist items, displaying moderate quality. Due to heterogeneity of studies, a qualitative synthesis was conducted. Cost ranges per outcome were enormous across different studies due to diversity in assumptions and model design. Pairwise comparisons of biologicals revealed conflicting results. Overall, adalimumab appeared to be most cost-effective (100% of all aggregated pairwise comparisons), followed by ustekinumab (66.7%), and infliximab (60%). However, in study conclusions most recent publications favored secukinumab and apremilast (75% and 60% of the studies investigating these medications). Accepted willingness-to-pay thresholds varied between 30,000 and 50,000 USD/Quality-Adjusted Life Year (QALY). Three-quarters of studies were financially supported, and in 90% of those, results were consistent with the funder’s interest. Economic evaluation of biologicals is crucial for responsible allocation of health care resources. In addition to summarizing the actual evidence this review highlights gaps and needs for future research.
“…). Twenty‐eight articles were published after the reviews that were conducted to inform the U.K.'s National Institute of Health and Care Excellence (NICE) guidelines for high‐quality psoriasis care . There was diversity in setting, perspective and national characteristics (Table ), psoriasis severity, design and evaluation type (Table S1; see Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Seven articles (14 of 71 comparisons) either did not specify disease severity or reported a mild to severe range. Chronic plaque psoriasis, the most common form, was considered in 13 articles (23 of 71 comparisons) . The remainder did not report the form of psoriasis.…”
Section: Resultsmentioning
confidence: 99%
“…This reflects trial designs that did not reflect routine practice or identify differences in outcomes relevant to patients, adherence and side‐effects over the lifetime course of psoriasis. A few studies addressed these issues using observational nonrandomized designs, postal survey or incorporation of long‐term safety monitoring data . It is unclear whether these designs were sufficient to minimize bias and accurately identify statistically valid differences between interventions.…”
The economic evidence is dominated by comparisons of interventions to placebo, with implicit comparisons of different therapies. There is a lack of evaluations of service model innovations to deliver complex packages of care for psoriasis. Primary and secondary integrated clinical and economic research is needed to address the limitations and to identify patient preferences and barriers/facilitators to treatment.
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