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本文引用的文献

1
Stratification, Hypothesis Testing, and Clinical Trial Simulation in Pediatric Drug Development.儿科药物研发中的分层、假设检验与临床试验模拟
Ther Innov Regul Sci. 2016;2016. doi: 10.1177/2168479016651661. Epub 2016 Jun 2.
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Biosimilars in rheumatic diseases: structural and functional variability that may impact clinical and regulatory decisions.风湿性疾病中的生物类似药:可能影响临床和监管决策的结构与功能变异性
Clin Rheumatol. 2016 Dec;35(12):2869-2875. doi: 10.1007/s10067-016-3430-7. Epub 2016 Oct 6.
3
Moving toward personalized medicine in rheumatoid arthritis: SNPs in methotrexate intracellular pathways are associated with methotrexate therapeutic outcome.迈向类风湿关节炎的个性化医疗:甲氨蝶呤细胞内途径中的单核苷酸多态性与甲氨蝶呤治疗效果相关。
Pharmacogenomics. 2016 Oct;17(15):1649-1674. doi: 10.2217/pgs-2016-0067. Epub 2016 Sep 27.
4
Clinical trials for authorized biosimilars in the European Union: a systematic review.欧盟已获批生物类似药的临床试验:一项系统综述
Br J Clin Pharmacol. 2016 Dec;82(6):1444-1457. doi: 10.1111/bcp.13076. Epub 2016 Sep 5.
5
The economic implications of biosimilars.生物类似药的经济影响。
Am J Manag Care. 2015 Dec;21(16 Suppl):s331-40.
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Use of Modeling and Simulation in the Design and Conduct of Pediatric Clinical Trials and the Optimization of Individualized Dosing Regimens.建模与仿真在儿科临床试验设计与实施以及个体化给药方案优化中的应用。
CPT Pharmacometrics Syst Pharmacol. 2015 Nov;4(11):630-40. doi: 10.1002/psp4.12038. Epub 2015 Nov 13.
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Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis: a randomised trial.泼尼松龙对比泼尼松龙联合环孢素 A 对比泼尼松龙联合甲氨蝶呤治疗新诊断的幼年皮肌炎:一项随机试验。
Lancet. 2016 Feb 13;387(10019):671-678. doi: 10.1016/S0140-6736(15)01021-1. Epub 2015 Nov 30.
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Clin Pharmacol Ther. 2016 Apr;99(4):363-9. doi: 10.1002/cpt.269. Epub 2015 Nov 9.
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青少年特发性关节炎的临床试验设计

Clinical Trial Design in Juvenile Idiopathic Arthritis.

作者信息

Balevic Stephen J, Becker Mara L, Cohen-Wolkowiez Michael, Schanberg Laura E

机构信息

Division of Pediatric Rheumatology, Duke University Medical Center, 2301 Erwin Road, CHC, T-Level, Durham, NC, 27710, USA.

Department of Pediatrics, Children's Mercy Kansas City, UMKC School of Medicine, 2401 Gillham Road, Kansas City, MO, 64108, USA.

出版信息

Paediatr Drugs. 2017 Oct;19(5):379-389. doi: 10.1007/s40272-017-0244-2.

DOI:10.1007/s40272-017-0244-2
PMID:28612093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6105333/
Abstract

Randomized clinical trials provide the gold standard evidence base to guide clinical practice. Despite major advances in trial design, pediatric clinical trials are still difficult to perform and pose unique challenges, including the need to consider the impact of developmental changes in trial design. Advances within pediatric rheumatology combined with the need to comply with legislative requirements have driven new approaches to performing pediatric clinical trials such as utilization of large research networks, incorporation of patient and family stakeholders in the planning and implementation of clinical trials, and the development of novel trial designs. The expansion of available biological therapeutics that now includes biosimilar drugs highlights the important and difficult balance of providing new and cost-effective drugs to children while ensuring safety in a vulnerable population. Future advances in juvenile idiopathic arthritis (JIA) clinical trials will likely be the application of precision medicine based on biologic, rather than phenotypic, classification of JIA, with improved understanding of pediatric clinical pharmacology. Clinical trial simulations and comparative effectiveness studies are important supplements to traditional clinical trials, permitting efficient studies and results that are more generalizable.

摘要

随机临床试验为指导临床实践提供了金标准证据基础。尽管试验设计取得了重大进展,但儿科临床试验仍然难以开展,并带来了独特的挑战,包括在试验设计中需要考虑发育变化的影响。儿科风湿病学的进展以及遵守立法要求的必要性推动了开展儿科临床试验的新方法,如利用大型研究网络、让患者和家庭利益相关者参与临床试验的规划和实施,以及开发新型试验设计。目前可用生物疗法的扩展,包括生物类似药,凸显了在为儿童提供新的且具成本效益的药物的同时确保弱势群体安全这一重要且困难的平衡。幼年特发性关节炎(JIA)临床试验未来的进展可能是基于JIA的生物学而非表型分类应用精准医学,同时加深对儿科临床药理学的理解。临床试验模拟和比较效果研究是传统临床试验的重要补充,能实现高效研究且结果更具普遍性。