First-in-human phase I open-label study of the LAG-3 antagonist antibody INCAGN02385 in patients with select advanced or metastatic solid tumors.

IF 4.8 2区 医学 Q1 ONCOLOGY
Oncologist Pub Date : 2025-07-04 DOI:10.1093/oncolo/oyaf136
John D Powderly, Martin E Gutierrez, Ani S Balmanoukian, Paul E Hoyle, Zhiwan Dong, Lulu Cheng, Xuejun Chen, John E Janik, Nawel Bourayou, Omid Hamid
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引用次数: 0

Abstract

Background: Immune checkpoint receptor lymphocyte-activation gene 3 (LAG-3) is an activation marker for CD4+ and CD8+ T cells. Prolonged LAG-3 expression downregulates T-cell activation; therefore, LAG-3 blockade may restore antitumor immune response. INCAGN02385 is a humanized monoclonal LAG-3-targeting antibody. This first-in-human phase I study evaluated INCAGN02385 for advanced/metastatic solid tumors.

Materials and methods: In this dose escalation study, patients with select immunogenic advanced or metastatic solid tumors received a single INCAGN02385 infusion (25 mg to 750 mg) every 2 weeks (Q2W). Objectives included evaluation of safety/tolerability, maximum tolerated dose (MTD) (primary), pharmacokinetics (PK), antitumor activity (secondary).

Results: Twenty-two patients were enrolled and treated. Sixty-four percent had received ≥ 3 lines of systemic therapy. Sixty-eight percent had received prior immune checkpoint inhibitor (ICI) therapy; anti-programmed death protein-1/anti-programmed death ligand-1, 68%, anti-cytotoxic T-lymphocyte-associated protein-4 therapy, 18%. No dose-limiting toxicities occurred, and an MTD was not reached. Sixteen patients (73%) experienced treatment-related adverse events (TRAEs), most frequently fatigue (n = 7). Except for one grade 3 lymphopenia TRAE, all were grade 1/2 severity. Two patients experienced sponsor-assessed immune-related AEs (pneumonitis, peripheral sensory neuropathy [n = 1] patient each). INCAGN02385 PK parameters were dose proportional across all doses evaluated. Six patients achieved stable disease lasting ≥ 56 days (range, 57-413 days).

Conclusions: INCAGN02385 exhibited linear PK and preliminary evidence of disease control in this heavily pretreated population, consistent with other LAG-3-targeting monotherapies. A 350-mg Q2W dose was selected for phase II studies that will focus on combinations of INCAGN02385 with other ICIs.

LAG-3拮抗剂INCAGN02385在晚期或转移性实体瘤患者中的首次人类I期开放标签研究。
背景:免疫检查点受体淋巴细胞激活基因3 (LAG-3)是CD4+和CD8+ T细胞的激活标志物。LAG-3长时间表达下调t细胞活化;因此,LAG-3阻断可能恢复抗肿瘤免疫反应。INCAGN02385是一种人源化单克隆lag -3靶向抗体。这项首次人体I期研究评估了INCAGN02385对晚期/转移性实体瘤的治疗作用。材料和方法:在这项剂量递增研究中,选择性免疫原性晚期或转移性实体瘤患者每2周(Q2W)接受一次INCAGN02385输注(25 mg至750 mg)。目的包括评估安全性/耐受性,最大耐受剂量(MTD)(主要),药代动力学(PK),抗肿瘤活性(次要)。结果:22例患者入组治疗。64%的患者接受了≥3线的全身治疗。68%的患者先前接受过免疫检查点抑制剂(ICI)治疗;抗程序性死亡蛋白-1/抗程序性死亡配体-1占68%,抗细胞毒性t淋巴细胞相关蛋白-4治疗占18%。没有发生剂量限制性毒性,也没有达到MTD。16名患者(73%)经历了治疗相关不良事件(TRAEs),最常见的是疲劳(n = 7)。除一例TRAE淋巴细胞减少症为3级外,其余均为1/2级。2例患者经历了由申办者评估的免疫相关不良事件(肺炎、周围感觉神经病变[n = 1]例)。INCAGN02385 PK参数在所有评估剂量中均成剂量比例。6例患者病情稳定,持续≥56天(范围:57-413天)。结论:在大量预处理的人群中,INCAGN02385表现出线性PK和疾病控制的初步证据,与其他靶向lag -3的单药治疗一致。选择350 mg Q2W剂量用于II期研究,重点是INCAGN02385与其他ICIs的联合使用。
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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来源期刊
Oncologist
Oncologist 医学-肿瘤学
CiteScore
10.40
自引率
3.40%
发文量
309
审稿时长
3-8 weeks
期刊介绍: The Oncologist® is dedicated to translating the latest research developments into the best multidimensional care for cancer patients. Thus, The Oncologist is committed to helping physicians excel in this ever-expanding environment through the publication of timely reviews, original studies, and commentaries on important developments. We believe that the practice of oncology requires both an understanding of a range of disciplines encompassing basic science related to cancer, translational research, and clinical practice, but also the socioeconomic and psychosocial factors that determine access to care and quality of life and function following cancer treatment.
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