Atopic Dermatitis Treatments Before and After Initiation of Ruxolitinib Cream: 6-Month Follow-Up Analysis of a US Payer Claims Database.

IF 2.2 Q3 HEALTH CARE SCIENCES & SERVICES ClinicoEconomics and Outcomes Research Pub Date : 2025-02-06 eCollection Date: 2025-01-01 DOI:10.2147/CEOR.S506043
Jinan Liu, Karishma Desai, Chia-Chen Teng, Daniel Sturm, Grace Stockbower, Hiten Patadia, Vincent Willey
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Abstract

Purpose: Many patients with atopic dermatitis (AD), a highly pruritic, relapsing, inflammatory skin disease, experience inadequate disease control. Ruxolitinib cream was approved in the US in September 2021 for the treatment of mild-to-moderate AD. This analysis describes treatment patterns before and after initiation of ruxolitinib cream among patients with AD.

Patients and methods: This retrospective, observational study used medical and pharmacy claims data from the Healthcare Integrated Research Database (HIRD®) and included adults and adolescents (aged ≥12 years) with an AD diagnosis, a first claim for ruxolitinib cream (index date) between October 2021 and July 2022, and continuous enrollment in a commercial or managed Medicare plan for 6 months before and after the index date. Analyses were also conducted in a subset of patients with a history of more advanced AD therapy (ie, systemic therapies, phototherapy, or ultrahigh-potent topical corticosteroids). Data from 6 months before ruxolitinib cream initiation (baseline period) and after initiation (follow-up period) were summarized using descriptive statistics.

Results: Of 1,581 patients in the overall AD cohort, 749 had a history of more advanced AD therapy. During the follow-up period, 43.8% of patients did not receive any other AD treatment. Compared with baseline, fewer patients received topical corticosteroids (52.3% vs 30.4%), topical calcineurin inhibitors (13.9% vs 6.6%), and topical phosphodiesterase-4 inhibitors (4.4% vs 2.3%) during the follow-up period; slightly greater reductions were observed among the subset with a history of more advanced AD therapies. Oral corticosteroid use decreased from 20.9% to 15.5% overall and from 44.1% to 20.7% in the subset with more advanced baseline therapy. Among patients receiving biologics at baseline, 17.4% did not receive these treatments during the follow-up period.

Conclusion: These 6-month follow-up data suggest that initiating ruxolitinib cream for AD may reduce the overall need for other topical treatments, oral corticosteroids, and biologics.

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开始使用 Ruxolitinib 霜前后的特应性皮炎治疗:对美国支付方索赔数据库的 6 个月随访分析。
目的:特应性皮炎(AD)是一种高度瘙痒、反复发作的炎症性皮肤病,许多患者的疾病控制不足。Ruxolitinib霜剂于2021年9月在美国被批准用于治疗轻中度AD。本分析描述了AD患者开始使用鲁索利替尼乳膏前后的治疗模式。患者和方法:这项回顾性观察性研究使用了来自医疗保健综合研究数据库(HIRD®)的医疗和药学索赔数据,纳入了患有AD诊断的成人和青少年(年龄≥12岁),首次索赔ruxolitinib乳膏(指标日期)为2021年10月至2022年7月,并在指标日期前后连续参加商业或管理医疗保险计划6个月。对一组接受过更高级AD治疗(即全身治疗、光疗或超高效局部皮质类固醇)的患者也进行了分析。采用描述性统计方法对鲁索利替尼乳膏开始使用前(基线期)和开始使用后(随访期)6个月的数据进行汇总。结果:在整个AD队列的1581例患者中,749例有更晚期AD治疗史。在随访期间,43.8%的患者未接受任何其他AD治疗。与基线相比,在随访期间,接受局部皮质类固醇(52.3%对30.4%)、局部钙调磷酸酶抑制剂(13.9%对6.6%)和局部磷酸二酯酶-4抑制剂(4.4%对2.3%)治疗的患者减少;在有更高级AD治疗史的亚组中观察到更大的减少。总体而言,口服皮质类固醇的使用从20.9%下降到15.5%,在基线治疗更先进的亚组中,口服皮质类固醇的使用从44.1%下降到20.7%。在基线接受生物制剂治疗的患者中,17.4%的患者在随访期间没有接受这些治疗。结论:这些6个月的随访数据表明,开始使用鲁索利替尼乳膏治疗AD可能会减少对其他局部治疗、口服皮质类固醇和生物制剂的总体需求。
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来源期刊
ClinicoEconomics and Outcomes Research
ClinicoEconomics and Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
3.70
自引率
0.00%
发文量
83
审稿时长
16 weeks
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