Safety and feasibility of 5T4 antibody-coupled allogeneic NK cell therapy for solid tumors: a first-in-human phase 1 trial.

IF 5.1
Liangjie Sun, Peiwen Ma, Zhenwei Miao, Na Su, Jinduo Bian, Shuhang Wang, Ning Li
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Abstract

Background: Patients with unresectable locally advanced or metastatic solid tumors have limited therapeutic options. Antibody-guided allogeneic natural killer (NK) cell therapy represents a novel immunotherapeutic strategy to enhance tumor targeting and cytotoxicity by coupling NK cells with tumor-specific antibodies targeting antigens such as 5T4.

Objective: To evaluate the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary efficacy of IBR854, a non-viral, non-genetically modified, 5T4 antibody-coupled allogeneic NK cell therapy, in patients with advanced solid tumors.

Patients and methods: This open-label, first-in-human phase 1 dose-escalation study enrolled 19 patients with unresectable locally advanced or metastatic solid tumors across five dose cohorts (3.0 × 109-12.0 × 109 cells per dose). Patients received intravenous IBR854 in a 3 + 3 escalation design. Safety, dose-limiting toxicities, adverse events, pharmacokinetics, anti-drug antibodies, and antitumor activity (RECIST v1.1) were assessed.

Results: No dose-limiting toxicities were observed. The most common treatment-emergent adverse events were elevated interleukin levels (42.1%), infusion-related reactions (31.6%), and fever (21.1%). No anti-drug antibodies were detected. The disease control rate was 43.8%. Median progression-free survival was 43 days. Pharmacokinetic analysis based on transgene copy number showed a dose-dependent prolongation of Tmax (0.867-3.433 h), with a relatively consistent half-life (1.390-2.648 h).

Conclusions: IBR854 demonstrated an acceptable safety and tolerability profile and achieved disease stabilization in a subset of heavily pretreated patients with advanced solid tumors. These findings support further clinical development of 5T4-targeted antibody-coupled allogeneic NK cell therapy. Trial registration This study was registered at ClinicalTrials.gov (registration number: NCT06001684).

5T4抗体偶联异体NK细胞治疗实体瘤的安全性和可行性:一项首次人体i期试验
背景:无法切除的局部晚期或转移性实体瘤患者的治疗选择有限。抗体引导的同种异体自然杀伤(NK)细胞治疗是一种新的免疫治疗策略,通过将NK细胞与靶向抗原(如5T4)的肿瘤特异性抗体偶联来增强肿瘤靶向性和细胞毒性。目的:评价IBR854(一种非病毒、非转基因、5T4抗体偶联的异体NK细胞疗法)在晚期实体瘤患者中的安全性、耐受性、药代动力学、免疫原性和初步疗效。患者和方法:这项开放标签、首次人体1期剂量递增研究纳入了19例不可切除的局部晚期或转移性实体瘤患者,分为5个剂量队列(每剂量3.0 × 109-12.0 × 109细胞)。患者在3 + 3升级设计中接受静脉注射IBR854。评估了安全性、剂量限制性毒性、不良事件、药代动力学、抗药物抗体和抗肿瘤活性(RECIST v1.1)。结果:未见剂量限制性毒性反应。最常见的治疗不良事件是白细胞介素水平升高(42.1%)、输液相关反应(31.6%)和发热(21.1%)。未检出抗药物抗体。疾病控制率为43.8%。中位无进展生存期为43天。基于转基因拷贝数的药代动力学分析显示,Tmax延长呈剂量依赖性(0.867-3.433 h),半衰期相对一致(1.390-2.648 h)。结论:IBR854显示出可接受的安全性和耐受性,并在大量预处理的晚期实体瘤患者中实现了疾病稳定。这些发现支持了5t4靶向抗体偶联异体NK细胞治疗的进一步临床发展。本研究已在ClinicalTrials.gov注册(注册号:NCT06001684)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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