Use of biologicals in dermatology – following the agreed path or going off-piste? A brief report

Pub Date : 2021-09-15 DOI:10.5639/gabij.2021.1003.018
M. Wilcock, A. Pothecary
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Abstract

Introduction: Biological medicines are used to treat a range of conditions according to National Institute for Health and Care Excellence (NICE) technology appraisals. The annual drug treatment cost per patient per year varies depending on various factors, including newer or older biological, and availability of a biosimilar. Our biologicals pathway for dermatology (moderate or severe psoriasis) listed less expensive older biologicals (including biosimilars) early on in the treatment choices and more recently approved (and generally more expensive) choices lower down the pathway. Objective: We aimed to identify which biologicals or selective immunosuppressants were used first line in adult patients with moderate or severe psoriasis, and ascertain if the reasons for use of treatments other than adalimumab were in accordance with the locally agreed pathway. Methods: Medical records were reviewed for a sample of patients prescribed biologicals during late 2019 and early 2020. We identified patients who had commenced any treatment. Contact was made with lead dermatology nurses if needed. Results: There were 33 patients commenced on a biological – 17 had newly started biological therapy and 16 had switched from a prior biological therapy to a new therapy. Of the 17 new patients, two commenced apremilast (biological contraindicated), 10 commenced adalimumab, and five commenced other biologicals. Of these five who commenced other biologicals, two were on guselkumab, two on ustekinumab, and one on certolizumab. In all five instances there was a valid reason for not using adalimumab as first choice though this was not always explicit in the multidisciplinary team (MDT) documentation. Discussion: Though the number of psoriasis patients (17) newly starting a biological medicine was relatively small, it was reassuring that for five of these who commenced a subcutaneous biological other than adalimumab, there was a valid reason for this choice, though not always explicit in the MDT letter, which Dermatology will ensure is clear for future decisions. Hence going ‘off-piste’ was deemed justified. Conclusion: This very small-scale study found that the local guideline was followed with patients commencing treatments other than biosimilar adalimumab for valid reasons.
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生物制剂在皮肤病学中的应用——遵循既定路线还是偏离正轨?简短的报告
导言:根据国家健康和护理卓越研究所(NICE)的技术评估,生物药物用于治疗一系列疾病。每位患者每年的药物治疗费用取决于各种因素,包括新生物或旧生物,以及生物仿制药的可用性。我们的皮肤病(中度或重度牛皮癣)生物制剂途径在早期的治疗选择中列出了较便宜的旧生物制剂(包括生物仿制药),以及最近批准的(通常更昂贵的)选择。目的:我们旨在确定哪些生物制剂或选择性免疫抑制剂在中度或重度牛皮癣成年患者中使用一线,并确定使用阿达木单抗以外的治疗方法的原因是否符合当地商定的途径。方法:对2019年底至2020年初使用生物制剂的患者样本进行病历回顾。我们确定了已开始任何治疗的患者。如有需要,与皮肤科主任护士联系。结果:33例患者开始接受生物治疗,其中17例是新开始的生物治疗,16例是从先前的生物治疗转向新的生物治疗。在17例新患者中,2例开始使用阿普米司特(生物学禁忌症),10例开始使用阿达木单抗,5例开始使用其他生物制剂。在这5名开始使用其他生物制剂的患者中,2人使用guselkumab, 2人使用ustekinumab, 1人使用certolizumab。在所有五个病例中,不使用阿达木单抗作为首选的正当理由,尽管这在多学科团队(MDT)文件中并不总是明确的。讨论:虽然新开始使用生物药物的牛皮癣患者(17例)数量相对较少,但令人欣慰的是,其中5例开始使用阿达木单抗以外的皮下生物药物治疗,这种选择是有正当理由的,尽管MDT信函中并不总是明确的,但皮肤科将确保未来的决定是明确的。因此,“离场”被认为是合理的。结论:这项非常小规模的研究发现,由于正当原因,患者开始接受阿达木单抗生物仿制药以外的治疗时,遵循了当地指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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