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解析单克隆抗体治疗药物监测的复杂性,实现肿瘤个体化剂量。

Unraveling the complexity of therapeutic drug monitoring for monoclonal antibody therapies to individualize dose in oncology.

机构信息

CRCT, Université de Toulouse, Inserm, and Institut Claudius-Regaud, IUCT-Oncopole, Toulouse, France.

Department of Pharmacy and Pharmacology and Department of Nuclear Medicine, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Pharmacol Res Perspect. 2021 Apr;9(2):e00757. doi: 10.1002/prp2.757.

Abstract

Monoclonal antibodies (Mabs) have become key drugs in cancer treatment, either as targeted therapies or more recently as immune checkpoint inhibitors (ICIs). The fact that only some patients benefit from these drugs poses the usual question in the field of onco-hematology: that of the benefit of individual dosing and the potential of therapeutic drug monitoring (TDM) to carry out this individualization. However, Mabs present unique pharmacological characteristics for TDM, and the pharmacokinetic-pharmacodynamic relationship observed should be interpreted differently than that observed for conventional drugs and small molecules. This pharmacology practice review has been summarized from a public debate between the authors at the International TDM and Clinical Toxicology meeting in Banff, 2020, regarding the potential roles of TDM in the Mab/ICI setting.

摘要

单克隆抗体(Mabs)已成为癌症治疗的关键药物,无论是作为靶向治疗药物还是最近的免疫检查点抑制剂(ICIs)。只有部分患者从中受益这一事实在肿瘤血液学领域提出了一个常见问题,即个体剂量的益处以及治疗药物监测(TDM)实现个体化的潜力。然而,Mabs 具有独特的 TDM 药理学特征,所观察到的药代动力学-药效学关系应与传统药物和小分子观察到的关系不同。该药理学实践综述是作者在 2020 年班夫国际 TDM 和临床毒理学会议上的公开辩论中总结的,内容涉及 TDM 在 Mab/ICI 环境中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41e0/7981594/6ae2da86d230/PRP2-9-e00757-g003.jpg

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