Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Roche Innovation Center Zürich, Roche Pharma Research and Early Development, Zürich, Switzerland.
Blood Adv. 2022 Feb 8;6(3):1025-1037. doi: 10.1182/bloodadvances.2021005954.
Glofitamab, a novel CD20xCD3, T-cell-engaging bispecific antibody, exhibited single-agent activity in Study NP30179, a first-in-human, phase 1 trial in relapsed/refractory B-cell non-Hodgkin lymphoma. Preclinical studies showed that glofitamab leads to T-cell activation, proliferation, and tumor cell killing upon binding to CD20 on malignant cells. Here, we provide evidence of glofitamab's clinical activity, including pharmacodynamic profile, mode of action, and factors associated with clinical response, by evaluating biomarkers in patient samples from the dose-escalation part of this trial. Patients enrolled in Study NP30179 received single-dose obinutuzumab pretreatment (1000 mg) 7 days before IV glofitamab (5 µg-25 mg). Glofitamab treatment lasted ≤12 cycles once every 2 or 3 weeks. Blood samples were collected at predefined time points per the clinical protocol; T-cell populations were evaluated centrally by flow cytometry, and cytokine profiles were analyzed. Immunohistochemical and genomic biomarker analyses were performed on tumor biopsy samples. Pharmacodynamic modulation was observed with glofitamab treatment, including dose-dependent induction of cytokines, and T-cell margination, proliferation, and activation in peripheral blood. Gene expression analysis of pretreatment tumor biopsy samples indicated that tumor cell intrinsic factors such as TP53 signaling are associated with resistance to glofitamab, but they may also be interlinked with a diminished effector T-cell profile in resistant tumors and thus represent a poor prognostic factor per se. This integrative biomarker data analysis provides clinical evidence regarding glofitamab's mode of action, supports optimal biological dose selection, and will further guide clinical development. This trial was registered at www.clinicaltrials.gov as #NCT03075696.
戈利木单抗是一种新型的 CD20xCD3,T 细胞结合双特异性抗体,在复发/难治性 B 细胞非霍奇金淋巴瘤的首次人体、I 期 NP30179 研究中表现出单药活性。临床前研究表明,戈利木单抗与恶性细胞上的 CD20 结合后,导致 T 细胞激活、增殖和肿瘤细胞杀伤。在这里,我们通过评估来自该试验剂量递增部分的患者样本中的生物标志物,提供了戈利木单抗的临床活性的证据,包括药效学特征、作用模式和与临床反应相关的因素。参加 NP30179 研究的患者接受了单剂量奥滨尤妥珠单抗预处理(1000 mg),在静脉注射戈利木单抗(5 µg-25 mg)前 7 天。戈利木单抗治疗持续≤12 个周期,每 2 或 3 周一次。根据临床方案预先设定时间点采集血样;通过流式细胞术对 T 细胞群进行中心评估,并分析细胞因子谱。对肿瘤活检样本进行免疫组织化学和基因组生物标志物分析。戈利木单抗治疗后观察到药效学调节,包括剂量依赖性诱导细胞因子,以及外周血中 T 细胞边缘、增殖和激活。预处理肿瘤活检样本的基因表达分析表明,肿瘤细胞内在因素(如 TP53 信号)与对戈利木单抗的耐药性相关,但它们也可能与耐药肿瘤中效应 T 细胞特征的减弱相关联,因此本身就是一个不良预后因素。这种综合生物标志物数据分析提供了关于戈利木单抗作用模式的临床证据,支持最佳生物学剂量选择,并将进一步指导临床开发。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT03075696。