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《实体器官移植中基于生物标志物的免疫抑制药物管理巴塞罗那共识》

Barcelona Consensus on Biomarker-Based Immunosuppressive Drugs Management in Solid Organ Transplantation.

作者信息

Brunet Mercè, Shipkova Maria, van Gelder Teun, Wieland Eberhard, Sommerer Claudia, Budde Klemens, Haufroid Vincent, Christians Uwe, López-Hoyos Marcos, Barten Markus J, Bergan Stein, Picard Nicolas, Millán López Olga, Marquet Pierre, Hesselink Dennis A, Noceti Ofelia, Pawinski Tomasz, Wallemacq Pierre, Oellerich Michael

机构信息

*Pharmacology and Toxicology Laboratory, Biomedical Diagnostic Center (CDB), Hospital Clinic of Barcelona, University of Barcelona, Spain; †Klinikum Stuttgart, ZentralInstitut für Klinische Chemie und Laboratoriumsmedizin, Stuttgart, Germany; ‡Departments of Internal Medicine and Hospital Pharmacy, Erasmus MC, University Medical Center Rotterdam, the Netherlands; §Department of Nephrology, University of Heidelberg, University Hospital Heidelberg and Mannheim, Heidelberg; ¶Medizinische Klinik mit Schwerpunkt Nephrologie, Charité Universitätsmedizin Berlin, Germany; ‖Louvain Centre for Toxicology and Applied Pharmacology, Institut de Recherche Expérimentale et Clinique and Clinical Chemistry Department, Université catholique de Louvain, Cliniques Universitaires Saint-Luc, Brussels, Belgium; **C42 Clinical Research & Development, Department of Anesthesiology, University of Colorado, Aurora; ††Immunology Laboratory, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain; ‡‡Department of Cardiovascular Surgery, University Heart Center Hamburg, Germany; §§Department of Pharmacology, Oslo University Hospital, Norway; ¶¶U850 INSERM, Université de Limoges, CHU Limoges, France; ‖‖Division of Nephrology and Renal Transplantation, Department of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, the Netherlands; ***Liver Diseases Department, National Center for Liver Transplantation, Hospital Central de las Fuerzas Armadas, Montevideo, Uruguay; †††Department of Drug Chemistry, Faculty of Pharmacy, Medical University of Warsaw, Poland; and ‡‡‡Department of Clinical Pharmacology, University Medical Center Göttingen, Georg-August University, Göttingen, Germany.

出版信息

Ther Drug Monit. 2016 Apr;38 Suppl 1:S1-20. doi: 10.1097/FTD.0000000000000287.

Abstract

With current treatment regimens, a relatively high proportion of transplant recipients experience underimmunosuppression or overimmunosuppression. Recently, several promising biomarkers have been identified for determining patient alloreactivity, which help in assessing the risk of rejection and personal response to the drug; others correlate with graft dysfunction and clinical outcome, offering a realistic opportunity for personalized immunosuppression. This consensus document aims to help tailor immunosuppression to the needs of the individual patient. It examines current knowledge on biomarkers associated with patient risk stratification and immunosuppression requirements that have been generally accepted as promising. It is based on a comprehensive review of the literature and the expert opinion of the Biomarker Working Group of the International Association of Therapeutic Drug Monitoring and Clinical Toxicology. The quality of evidence was systematically weighted, and the strength of recommendations was rated according to the GRADE system. Three types of biomarkers are discussed: (1) those associated with the risk of rejection (alloreactivity/tolerance), (2) those reflecting individual response to immunosuppressants, and (3) those associated with graft dysfunction. Analytical aspects of biomarker measurement and novel pharmacokinetic-pharmacodynamic models accessible to the transplant community are also addressed. Conventional pharmacokinetic biomarkers may be used in combination with those discussed in this article to achieve better outcomes and improve long-term graft survival. Our group of experts has made recommendations for the most appropriate analysis of a proposed panel of preliminary biomarkers, most of which are currently under clinical evaluation in ongoing multicentre clinical trials. A section of Next Steps was also included, in which the Expert Committee is committed to sharing this knowledge with the Transplant Community in the form of triennial updates.

摘要

在当前的治疗方案下,相当一部分移植受者经历免疫抑制不足或过度免疫抑制。最近,已确定了几种有前景的生物标志物来确定患者的同种异体反应性,这有助于评估排斥风险和个体对药物的反应;其他生物标志物与移植物功能障碍和临床结果相关,为个性化免疫抑制提供了切实可行的机会。本共识文件旨在帮助根据个体患者的需求调整免疫抑制方案。它审视了与患者风险分层和免疫抑制需求相关的生物标志物的现有知识,这些知识已被普遍认为具有前景。它基于对文献的全面综述以及国际治疗药物监测和临床毒理学协会生物标志物工作组的专家意见。对证据质量进行了系统加权,并根据GRADE系统对推荐强度进行了评级。讨论了三种类型的生物标志物:(1)与排斥风险相关的生物标志物(同种异体反应性/耐受性),(2)反映个体对免疫抑制剂反应的生物标志物,以及(3)与移植物功能障碍相关的生物标志物。还讨论了生物标志物测量的分析方面以及移植界可获取的新型药代动力学 - 药效学模型。传统的药代动力学生物标志物可与本文讨论的生物标志物联合使用,以实现更好的结果并提高移植物长期存活率。我们的专家小组对一组拟议的初步生物标志物的最合适分析提出了建议,其中大多数目前正在正在进行的多中心临床试验中进行临床评估。还包括了“下一步”部分,专家委员会承诺每三年更新一次,以向移植界分享这些知识。

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