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贝伐单抗在遗传性出血性毛细血管扩张症中的剂量-反应关系

Dose - response relationship of bevacizumab in hereditary hemorrhagic telangiectasia.

作者信息

Azzopardi Nicolas, Dupuis-Girod Sophie, Ternant David, Fargeton Anne-Emmanuelle, Ginon Isabelle, Faure Frédéric, Decullier Evelyne, Roux Adeline, Carette Marie-France, Gilbert-Dussardier Brigitte, Hatron Pierre-Yves, Lacombe Pascal, Leguy-Seguin Vanessa, Rivière Sophie, Corre Romain, Bailly Sabine, Paintaud Gilles

机构信息

a Université François-Rabelais de Tours ; CNRS, GICC UMR 7292; Tours , France.

出版信息

MAbs. 2015;7(3):630-7. doi: 10.1080/19420862.2015.1022693.

Abstract

Hereditary hemorrhagic telangiectasia (HHT), a genetic vascular disorder associated with epistaxis and hepatic shunts, is responsible for high-output cardiac failure in rare cases. Bevacizumab, which targets vascular endothelial growth factor, was shown to decrease both cardiac index (CI) and epistaxis duration in HHT patients with severe liver involvement. The relationship between its serum concentration and change in both CI and epistaxis duration was investigated to design the bevacizumab maintenance dosing regimen of future therapeutic studies. Twenty-five HHT patients with dyspnea and high CI were included in a prospective non-comparative study. They received bevacizumab at a dose of 5 mg/kg per infusion every 14 days for a total of 6 injections. The relationships between bevacizumab serum concentration and both CI and epistaxis duration were described using transit compartments and direct inhibition pharmacokinetic-pharmacodynamic models. The performances of different maintenance regimens were evaluated using simulation. Infusions every 3, 2 and one months were predicted to maintain 41%, 45% and 50% of patients with CI <4 L/min/m(2) at 24 months, respectively. The fraction of patients with <20 min epistaxis per month was predicted to be 34%, 43% and 60%, with infusion every 3, 2 or one months, respectively. Simulations of the effects of different maintenance dosing regimens predict that monthly 5 mg/kg infusions of bevacizumab should allow sustained control of both cardiac index and epistaxis.

摘要

遗传性出血性毛细血管扩张症(HHT)是一种与鼻出血和肝分流相关的遗传性血管疾病,在罕见情况下可导致高输出量心力衰竭。贝伐单抗靶向血管内皮生长因子,已证明可降低严重肝脏受累的HHT患者的心脏指数(CI)和鼻出血持续时间。研究了其血清浓度与CI和鼻出血持续时间变化之间的关系,以设计未来治疗研究的贝伐单抗维持给药方案。一项前瞻性非对照研究纳入了25例有呼吸困难和高CI的HHT患者。他们接受每14天一次、每次剂量为5mg/kg的贝伐单抗静脉输注,共6次。使用转运室和直接抑制药代动力学-药效学模型描述了贝伐单抗血清浓度与CI和鼻出血持续时间之间的关系。使用模拟评估了不同维持方案的效果。预测每3个月、每2个月和每月进行一次输注,在24个月时分别可使41%、45%和50%的CI<4L/min/m²的患者维持该水平。预测每月鼻出血时间<20分钟的患者比例,每3个月、每2个月或每月进行一次输注时分别为34%、43%和60%。不同维持给药方案效果的模拟预测,每月5mg/kg的贝伐单抗输注应能持续控制心脏指数和鼻出血。

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