Comparing the efficacy of cipaglucosidase alfa plus miglustat with alglucosidase alfa for late-onset Pompe disease: an expanded network meta-analysis utilizing patient-level and aggregate data.

IF 2.8 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES
Shuai Fu, Noemi Hummel, Simon Shohet, Neil Johnson, Alasdair MacCulloch, Jeff Castelli, William Kerr, Brian Fox, Vera Gielen
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引用次数: 0

Abstract

Aim: Treatment options for late-onset Pompe disease (LOPD) include enzyme replacement therapy (ERT) with alglucosidase alfa (alg), cipaglucosidase alfa plus miglustat (cipa + mig) and avalglucosidase alfa. However, only one randomized controlled trial (RCT) directly compared cipa + mig and alg and had relatively few ERT-naive patients. A multilevel network meta-regression (ML-NMR) integrated individual patient data and aggregate data into indirect treatment comparisons, with relative effects adjusted to any target population, to compare the efficacy of cipa + mig and alg. Materials & methods: A Bayesian ML-NMR was conducted to compare the efficacy of cipa + mig and alg for 6-minute walk distance (6MWD, meters) and percent predicted forced vital capacity (ppFVC) across any target population, using patient-level and aggregate data from RCTs (PROPEL, COMET, LOTS) and phase I/II and open-label extension (OLE) trials (PROPEL OLE, LOTS OLE, COMET OLE, ATB200-02, NEO-1/NEO-EXT), adjusting for baseline covariates. Relative effect estimates were obtained for 6MWD and ppFVC change from baseline to week 52. Two networks were analyzed: network A (RCTs only) and network B (RCTs and single-arm OLE and phase I/II studies matched to comparator arms). To assess the impact of prior ERT exposure, simulations were conducted by only varying ERT duration among included covariates. Results: For cipa + mig compared with alg, both networks were associated with relative increases in 6MWD (mean difference [95% credible interval], Bayesian probability for network A: 13.48 m [6.79, 19.85], >99.9%; network B: 12.59 m [7.89, 17.45], >99.9%) and ppFVC (network A: 1.63% [0.71, 2.60], >99.9%; network B: 3.17% [2.53, 3.81], >99.9%). Network B suggested cipa + mig was favorable (>99.9%) in all groups for both end points and appeared more favorable with increasing ERT duration. Conclusion: Cipa + mig was associated with an improvement in 6MWD and ppFVC relative to alg independent of prior ERT exposure, which appeared more favorable when all available evidence was used. These data could inform decision-making in treating ERT-naive and ERT-experienced patients with LOPD.

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比较西葡萄糖苷酶加米卢司他与α葡萄糖苷酶治疗迟发性庞贝病的疗效:一项利用患者水平和汇总数据的扩展网络meta分析。
目的:迟发性Pompe病(LOPD)的治疗选择包括alfa (alg)、cipa + miglustat (cipa + mig)和avalglucosidase alfa的酶替代疗法(ERT)。然而,只有一项随机对照试验(RCT)直接比较了cipa + mig和alg,并且相对较少的ert初始患者。多层次网络meta回归(ML-NMR)将个体患者数据和总体数据整合到间接治疗比较中,并将相对效应调整到任何目标人群,以比较cipa + mig和alg的疗效。材料和方法:使用随机对照试验(PROPEL、COMET、LOTS)、I/II期和开放标签扩展(OLE)试验(PROPEL OLE、LOTS OLE、COMET OLE、ATB200-02、NEO-1/NEO-EXT)的患者水平和汇总数据,对基线共变量进行调整,进行贝叶斯ML-NMR,比较cipa + mg和alg对6分钟步行距离(6MWD,米)和预测强制肺泡容量百分比(ppFVC)在任何目标人群中的疗效。从基线到第52周,获得了6MWD和ppFVC变化的相对效应估计。分析了两个网络:网络A(仅rct)和网络B (rct和单臂OLE以及与比较组匹配的I/II期研究)。为了评估先前ERT暴露的影响,模拟仅通过在纳入的协变量中改变ERT持续时间来进行。结果:cipa + mig与alg相比,两种网络的6MWD(平均差值[95%可信区间],网络A的贝叶斯概率为13.48 m[6.79, 19.85], >99.9%;网络B的贝叶斯概率为12.59 m[7.89, 17.45], >99.9%)和ppFVC(网络A: 1.63%[0.71, 2.60], >99.9%;网络B: 3.17%[2.53, 3.81], >99.9%)相对增加。网络B显示,在所有组中,cipa + mig在两个终点都是有利的(>99.9%),并且随着ERT持续时间的增加而更加有利。结论:与先前ERT暴露无关,Cipa + mig与6MWD和ppFVC的改善相关,当使用所有可用证据时,这似乎更有利。这些数据可以为治疗未ert和已ert的LOPD患者提供决策依据。
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来源期刊
Journal of comparative effectiveness research
Journal of comparative effectiveness research HEALTH CARE SCIENCES & SERVICES-
CiteScore
3.50
自引率
9.50%
发文量
121
期刊介绍: Journal of Comparative Effectiveness Research provides a rapid-publication platform for debate, and for the presentation of new findings and research methodologies. Through rigorous evaluation and comprehensive coverage, the Journal of Comparative Effectiveness Research provides stakeholders (including patients, clinicians, healthcare purchasers, and health policy makers) with the key data and opinions to make informed and specific decisions on clinical practice.
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