A comparison of liprotamase, a non-porcine pancreatic enzyme replacement therapy, to porcine extracted pancrelipase in a noninferiority randomized clinical trial in patients with cystic fibrosis
M. Konstan, J. Wagener, M. Wilschanski, I. Laki, S. Boas, S. Dorota, M. Gangal, R. S. Martin, W. Shanahan, J. Pennington
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引用次数: 3
Abstract
Objective: Porcine derived enzymes are used for pancreatic enzyme replacement therapy in patients with cystic fibrosis (CF). Liprotamase is a biotechnology-derived, non-porcine, enzyme replacement without enteric coating. This study compared the effects of liprotamase and porcinederived pancrelipase on Coefficient of Fat Absorption (CFA) in patients with Exocrine Pancreatic Insufficiency (EPI) due to CF. Methods: We conducted a randomized, open-label, assessor blind, parallel group, multicenter, international trial to evaluate the noninferiority of liprotamase to porcine pancrelipase in 128 CF patients’ age ≥7 years with pancreatic insufficiency (Study NCT02279498). Subjects were randomized to liprotamase or pancrelipase, dose-matched to pre-study lipase doses. The primary endpoint was the between group difference in least square (LS) mean change from baseline in CFA, with a non-inferiority margin of -15% for the lower bound of the 95% confidence interval (CI). Key secondary endpoints compared treatment effects on CFA in the absence or presence of concomitant gastric acid suppression (GAS), and coefficient of nitrogen absorption (CNA). Results: Liprotamase missed the noninferiority criterion for CFA (95% CI -16.0, -7.7%), but met that criterion for CNA (95% CI -1.9, -0.7%). Concomitant GAS was associated with higher CFA with liprotamase but not pancrelipase. Conclusion: In this study, liprotamase was inferior to pancrelipase with regards to CFA, but not CNA. Higher doses and GAS may improve the efficacy of liprotamase.
目的:猪源性酶用于囊性纤维化(CF)患者胰酶替代治疗。利朊酶是一种生物技术衍生的,非猪的,不含肠道包衣的酶替代品。本研究比较了利protamase和猪源性胰酶对CF所致外分泌胰功能不全(EPI)患者脂肪吸收系数(CFA)的影响。方法:我们进行了一项随机、开放标签、评估者盲、平行组、多中心、国际试验,评估128例年龄≥7岁的CF伴胰功能不全患者使用利protamase对猪源性胰酶的非效性(研究NCT02279498)。受试者被随机分配到脂肪酶或胰酶组,剂量与研究前的脂肪酶剂量相匹配。主要终点是CFA中最小二乘(LS)平均变化与基线的组间差异,95%置信区间(CI)下界的非劣效裕度为-15%。关键次要终点比较了在没有或存在胃酸抑制(GAS)和氮吸收系数(CNA)的情况下对CFA的治疗效果。结果:利普塔酶未达到CFA的非劣效性标准(95% CI -16.0, -7.7%),但达到了CNA的标准(95% CI -1.9, -0.7%)。伴随的GAS与较高的CFA与利朊酶相关,但与胰酶无关。结论:本研究中,对于CFA,利普曲酶不如胰酶,而对于CNA,则不如胰酶。高剂量和GAS可提高利朊酶的疗效。