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替雷利珠单抗治疗实体瘤或血液系统恶性肿瘤患者的临床剂量依据。

Clinical dose rationale of tislelizumab in patients with solid or hematological advanced tumors.

机构信息

BeiGene USA, Inc., San Mateo, California, USA.

BeiGene USA, Inc., Cambridge, Massachusetts, USA.

出版信息

Clin Transl Sci. 2024 Mar;17(3):e13769. doi: 10.1111/cts.13769.

Abstract

Tislelizumab, an anti-programmed cell death protein 1 monoclonal antibody, has demonstrated improved survival benefits over standard of care for multiple cancer indications. We present the clinical rationale and data supporting tislelizumab dose recommendation in patients with advanced tumors. The phase I, first-in-human, dose-finding BGB-A317-001 study (data cutoff [DCO]: August 2017) examined the following tislelizumab dosing regimens: 0.5-10 mg/kg every 2 weeks (q2w), 2-5 mg/kg q2w or q3w, and 200 mg q3w. Similar objective response rates (ORRs) were reported in the 2 and 5 mg/kg q2w or q3w cohorts. Safety outcomes (grade ≥3 adverse events [AEs], AEs leading to dose modification/discontinuation, immune-mediated AEs, and infusion-related reactions) were generally comparable across the dosing range examined. These results, alongside the convenience of a fixed q3w dose, formed the basis of choosing 200 mg q3w as the recommended dosing regimen for further clinical use. Pooled exposure-response (E-R) analyses by logistic regression using data from study BGB-A317-001 (DCO: August 2020) and three additional phase I/II studies (DCOs: 2018-2020) showed no statistically significant correlation between tislelizumab pharmacokinetic exposure and ORR across multiple solid tumor types or classical Hodgkin's lymphoma, nor was exposure associated with any of the safety end points evaluated over the dose range tested. Hence, tislelizumab showed a relatively flat E-R relationship. Overall, the totality of data, including efficacy, safety, and E-R analyses, together with the relative convenience of a fixed q3w dose, provided clinical rationale for the recommended dosing regimen of tislelizumab 200 mg q3w for multiple cancer indications.

摘要

替雷利珠单抗是一种抗程序性细胞死亡蛋白 1 单克隆抗体,在多种癌症适应证中,与标准治疗相比,它显示出了提高生存率的益处。我们提出了支持替雷利珠单抗在晚期肿瘤患者中剂量推荐的临床原理和数据。I 期、首次人体、剂量发现的 BGB-A317-001 研究(数据截止日期 [DCO]:2017 年 8 月)研究了以下替雷利珠单抗给药方案:0.5-10mg/kg,每 2 周(q2w),2-5mg/kg,q2w 或 q3w,以及 200mg,q3w。在 2mg/kg 和 5mg/kg,q2w 或 q3w 队列中,报告了相似的客观缓解率(ORR)。安全性结果(≥3 级不良事件 [AE]、导致剂量调整/中断的 AE、免疫介导的 AE 和输注相关反应)在整个研究范围内基本相似。这些结果,以及 q3w 固定剂量的便利性,构成了选择 200mg,q3w 作为进一步临床使用的推荐剂量方案的基础。使用来自 BGB-A317-001 研究(DCO:2020 年 8 月)和另外三项 I/II 期研究(DCOs:2018-2020 年)的数据进行逻辑回归的汇总暴露-反应(E-R)分析表明,替雷利珠单抗药代动力学暴露与多种实体瘤类型或经典霍奇金淋巴瘤的 ORR 之间没有统计学上的显著相关性,也没有与测试剂量范围内评估的任何安全性终点相关。因此,替雷利珠单抗表现出相对平坦的 E-R 关系。总体而言,数据的整体情况,包括疗效、安全性和 E-R 分析,以及 q3w 固定剂量的相对便利性,为替雷利珠单抗用于多种癌症适应证的推荐剂量方案 200mg,q3w 提供了临床依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0968/10958174/e22142ddba00/CTS-17-e13769-g002.jpg

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