在 WAPPS-Hemo 平台内开发支持对缺乏血浆酶原的患者进行预防性替代治疗的血浆酶原人群 PK 模型

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-05-02 DOI:10.1111/hae.15027
Pierre Chelle, Dagmar Hajducek, Karen Thibaudeau, Nicholas Hobson, Alfonso Iorio, Amy Shapiro, Andrea Edginton
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引用次数: 0

摘要

导言胰蛋白酶原缺乏症是一种极为罕见的疾病,患者如不及时治疗可能会出现韧带病变。本研究的目的是开发、评估并在 WAPPS-Hemo 平台中整合支持血浆酶原缺乏症患者预防性替代治疗的人群 PK 模型。结果该人群 PK 模型来自先前临床研究中的 16 名参与者,是一个 2 室模型,其变异性用去脂质量来描述最为恰当。评估结果表明,该模型很好地描述了数据,在有限的采样环境中进行贝叶斯预测,可使与纤溶酶原治疗相关的PK参数达到可接受的精度。结论该模型已被整合到WAPPS-Hemo网络服务中,以帮助纤溶酶原缺乏患者进行个体化预防治疗。通过 WAPPS-Hemo 数据库收集的前瞻性 PK 数据将用于更好地了解纤溶酶原 PK 和改善患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of a Plasminogen Population PK model supporting prophylactic replacement therapy for Plasminogen deficient patients within the WAPPS-Hemo platform

Development of a Plasminogen Population PK model supporting prophylactic replacement therapy for Plasminogen deficient patients within the WAPPS-Hemo platform

Introduction

Plasminogen deficiency is an ultra rare disease whose patients may develop ligneous lesions if untreated. Prophylactic replacement therapy with plasma derived plasminogen, Ryplazim, is efficient in treating lesions and could benefit from pharmacokinetic (PK) tailoring.

Aim

The objectives of this study are to develop, evaluate and integrate into the WAPPS-Hemo platform a Population PK model supporting prophylactic replacement therapy for Plasminogen deficient patients.

Methods

Population PK modelling and evaluations followed the same protocol performed for factor VIII and IX concentrates. Limited sampling analysis used dosing and sampling scenarios in accordance with recommended treatment for Ryplazim.

Results

The population PK model, derived from 16 participants included in previous clinical studies, was a 2-compartment model whose variability was best described by fat-free mass. Evaluations showed that the model described well the data and Bayesian forecasting in limited sampling environment led to acceptable precision for PK parameters relevant to plasminogen treatment.

Conclusion

The model was integrated into the WAPPS-Hemo webservice to help individualize prophylactic treatment in plasminogen deficient patients. Prospective PK data to be collected through the WAPPS-Hemo database will be used to better understand plasminogen PK and improve patient care.

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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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