Case report of fatal immune-mediated myocarditis following treatment with davoceticept (ALPN-202), a PD-L1-dependent CD28 costimulator and dual PD-L1/CTLA-4 checkpoint inhibitor, in combination with pembrolizumab.

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Ludimila Cavalcante, Sreenivasa Chandana, Nehal Lakhani, Amanda Enstrom, Heidi LeBlanc, Joseph Schmalz, Krisztina Lengyel, Frank Schneider, Heather Thomas, Michael J Chisamore, Stanford L Peng, Allison Naumovski, Diwakar Davar
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引用次数: 0

Abstract

Engagement of programmed death-1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) can interfere with the CD28 signaling requisite for T-cell activation. While immune checkpoint inhibitors (ICIs) can relieve this suppression, they are unable to drive CD28 costimulation that may mechanistically contribute to ICI resistance. Thus, CD28 costimulation in the context of checkpoint inhibition may activate immunosuppressed T-cells in the tumor microenvironment. Davoceticept (ALPN-202) is an Fc fusion of a CD80 variant immunoglobulin domain (vIgD) designed to mediate PD-L1-dependent CD28 costimulation while inhibiting the PD-L1 and CTLA-4 checkpoints. PD-L1-restriction of davoceticept's CD28 costimulatory activity may minimize systemic T-cell activation and avoid untoward systemic toxicities. At the same time, preclinical studies have suggested that treatment with davoceticept during PD-1 inhibition may enhance antitumor activity by upregulating PD-L1, potentially synergizing with davoceticept's PD-L1-dependent costimulatory mechanism. This report details two cases of fatal cardiac events following treatment with davoceticept in combination with pembrolizumab (anti-PD-1) in the phase 1 study, NEON-2. Both events occurred in females in their 60s; one with choroidal melanoma and prior immunotherapy, the other with ICI-naïve microsatellite stable colorectal cancer. The clinical courses were fulminant with symptom onset at 2 weeks, followed by rapid decline. Cardiac autopsy from one patient confirmed immune-related myocarditis, and immunosequencing revealed expansion of a single T-cell clone that was not present in the pretreatment tumor. These cases highlight the importance of understanding risk factors that may contribute to immune-related myocarditis and other severe immune-related adverse events when CD28 agonism is targeted in the context of checkpoint inhibition.NEON-2 (NCT04920383).

PD-L1依赖性CD28成本刺激剂和PD-L1/CTLA-4双重检查点抑制剂davoceticept (ALPN-202)联合pembrolizumab治疗后发生致命性免疫介导性心肌炎的病例报告。
程序性死亡-1(PD-1)和细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)的参与会干扰 T 细胞活化所需的 CD28 信号传导。虽然免疫检查点抑制剂(ICIs)可以缓解这种抑制,但它们无法驱动CD28成本刺激,而CD28成本刺激可能从机理上导致ICI耐药。因此,在检查点抑制的背景下,CD28成本刺激可能会激活肿瘤微环境中免疫抑制的T细胞。Davoceticept(ALPN-202)是CD80变异免疫球蛋白结构域(vIgD)的Fc融合物,旨在介导依赖于PD-L1的CD28成本刺激,同时抑制PD-L1和CTLA-4检查点。PD-L1对davoceticept的CD28成本刺激活性的限制可能会最大限度地减少全身T细胞的激活,避免不良的全身毒性。同时,临床前研究表明,在PD-1抑制期间使用达伐西肽治疗可能会通过上调PD-L1增强抗肿瘤活性,从而与达伐西肽的PD-L1依赖性成本刺激机制产生协同作用。本报告详细介绍了在一期研究 NEON-2 中,davoceticept 与 pembrolizumab(抗 PD-1)联合治疗后发生的两例致命心脏事件。这两起事件均发生在60多岁的女性身上;其中一人患有脉络膜黑色素瘤并曾接受过免疫疗法,另一人患有ICI无效的微卫星稳定型结直肠癌。临床病程为暴发性,2周后出现症状,随后迅速衰退。一名患者的心脏解剖证实了与免疫相关的心肌炎,免疫测序发现了治疗前肿瘤中不存在的单个T细胞克隆的扩增。这些病例凸显了了解在检查点抑制背景下CD28激动剂靶向治疗时可能导致免疫相关性心肌炎和其他严重免疫相关不良事件的风险因素的重要性。
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
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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