Pharmacology Department, U1030 INSERM, University Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif, France.
Laboratory for Immunomonitoring in Oncology (LIO), Faculty of Pharmacy, University Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif, France.
J Hematol Oncol. 2022 Jan 15;15(1):6. doi: 10.1186/s13045-021-01182-3.
Anti-CTLA-4 and anti-PD-1/PD-L1 immune checkpoint inhibitors are therapeutic monoclonal antibodies that do not target cancer cells but are designed to reactivate or promote antitumor immunity. Dosing and scheduling of these biologics were established according to conventional drug development models, even though the determination of a maximum tolerated dose in the clinic could only be defined for anti-CTLA-4. Given the pharmacology of these monoclonal antibodies, their high interpatient pharmacokinetic variability, the actual clinical benefit as monotherapy that is observed only in a specific subset of patients, and the substantial cost of these treatments, a number of questions arise regarding the selected dose and the dosing interval. This review aims to outline the development of these immunotherapies and considers optimization options that could be used in clinical practice.
抗 CTLA-4 和抗 PD-1/PD-L1 免疫检查点抑制剂是治疗性单克隆抗体,它们并非针对癌细胞,而是旨在重新激活或促进抗肿瘤免疫。这些生物制剂的剂量和方案是根据传统的药物开发模型确定的,尽管在临床上只能确定抗 CTLA-4 的最大耐受剂量。鉴于这些单克隆抗体的药理学特性、它们在患者间高度的药代动力学变异性、仅在特定患者亚群中观察到的作为单药治疗的实际临床获益,以及这些治疗的高昂成本,对于所选剂量和给药间隔存在许多问题。本文旨在概述这些免疫疗法的发展,并考虑在临床实践中可以使用的优化选择。