评估针对杜兴氏肌肉萎缩症患者的磷酰二氨吗啉寡聚体治疗模式:MarketScan索赔分析。

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Therapy Pub Date : 2024-11-11 DOI:10.1007/s12325-024-03044-z
Alexa C Klimchak, James Signorovitch, Bryan Innis, Chamindra G Laverty, Katherine Gooch
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引用次数: 0

摘要

简介:磷酰二胺吗啉寡聚物(PMOs)是一种基于体重的治疗方法,每周通过静脉输注给药,在美国已被批准用于治疗杜氏肌营养不良症(DMD)患者,这些患者可接受某些外显子跳接治疗。现实世界中有关 PMO 治疗模式的证据十分有限。本研究使用纵向行政报销数据来描述美国 DMD 患者的 PMO 治疗模式:MarketScan® 商业和医疗补助数据(2018 年 1 月 1 日至 2021 年 12 月 31 日)用于识别 PMO 治疗(依替普生、戈罗迪生、维托拉生、卡西美生)的索赔。研究描述了报销天数比例(PDC)、连续报销 PMO 的比例(报销间隔不超过 30 天)以及 PMO 报销间隔≥30 天后的后续 PMO 报销时间:结果:133 名患者的 PMO 索偿次数≥ 1 次。需要多个代码才能确定 PMO 治疗范围。平均年龄为 14.1 岁;所有患者均为男性。平均连续随访时间为 669.3 天。PDC 中位数为 83.4%。74名患者(55.6%)拥有连续的PMO报销范围(报销间隔不≥30天)。在 59 名 PMO 索偿间隔≥30 天的患者中,39 名患者的后续 PMO 索偿间隔≥1 天。通过卡普兰-梅耶尔分析计算剔除率,75.5%的患者在间隔期≥30天后的1年内进行了后续PMO索赔,中位时间为64天(包括符合条件的30天):结论:了解治疗模式对于描述精准基因药物在现实世界中的使用情况非常重要。本研究观察到,PMO 治疗 DMD 的 PDC 较高。大多数患者都有持续的 PMO 治疗申请,而大多数在 PMO 治疗申请中出现空白的患者都有后续的 PMO 治疗申请。尽管如此,考虑到理赔数据的不足和支付方承保范围的因素,所观察到的持续性可能被低估了。对于以体重为基础的输注式 PMO 治疗,如果仅根据索赔数据观察到的治疗模式来推断治疗效果或耐受性,应谨慎行事。
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Assessment of Phosphorodiamidate Morpholino Oligomer Treatment Patterns for Patients with Duchenne Muscular Dystrophy: A MarketScan Claims Analysis.

Introduction: Phosphorodiamidate morpholino oligomers (PMOs), weight-based treatments administered weekly by intravenous infusion, are approved in the US for patients with Duchenne muscular dystrophy (DMD) amenable to certain exon skipping. Evidence regarding PMO treatment patterns in real-world settings is limited. This study used longitudinal administrative claims data to characterize PMO treatment patterns among US patients with DMD.

Methods: MarketScan® commercial and Medicaid data (January 1, 2018-December 31, 2021) were used to identify claims for PMO treatments (eteplirsen, golodirsen, viltolarsen, casimersen). The proportion of days covered (PDC), proportion with continuous PMO claims coverage (no gaps in claims ≥ 30 days), and time to subsequent PMO claims after a ≥ 30-day gap in PMO claims were described.

Results: One hundred thirty-three patients with ≥ 1 PMO claim were identified. Multiple codes were needed to identify PMO treatment coverage. Mean age was 14.1 years; all patients were male. Mean continuous follow-up duration was 669.3 days. Median PDC was 83.4%. Seventy-four (55.6%) patients had continuous PMO claims coverage (no ≥ 30-day gaps in claims). Of the 59 patients with ≥ 1 gap in PMO claims of ≥ 30 days, 39 had ≥ 1 subsequent PMO claim. Accounting for censoring via Kaplan-Meier analysis, 75.5% had a subsequent PMO claim within 1 year after a ≥ 30-day gap, with a median time of 64 days (including the qualifying 30 days).

Conclusion: Understanding treatment patterns is important for characterizing real-world utilization of precision genetic medicines. This study observed a high PDC for PMO treatments for DMD. Most patients had continuous PMO claims coverage, and most patients with a gap in PMO claims had a subsequent PMO claim. Nonetheless, the observed persistence may have been underestimated given shortcomings of claims data and payer coverage considerations. Caution should be exercised when inferring treatment effectiveness or tolerability based on observed treatment patterns from claims data alone for weight-based, infused PMO treatments.

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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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