TIMEPOINT是一项联合MTL-CEBPA与派姆单抗的i期研究,支持MTL-CEBPA在实体瘤中的免疫调节作用。

IF 11.7 1区 医学 Q1 CELL BIOLOGY
Ruth Plummer, Mikael H Sodergren, Rose Hodgson, Bríd M Ryan, Nina Raulf, Joanna P Nicholls, Vikash Reebye, Jon Voutila, Laura Sinigaglia, Tim Meyer, David J Pinato, Debashis Sarker, Bristi Basu, Sarah Blagden, Natalie Cook, Thomas R Jeffrey Evans, Jeffrey Yachnin, Cheng E Chee, Daneng Li, Anthony El-Khoueiry, Maria Diab, Kai-Wen Huang, Madhava Pai, Duncan Spalding, Thomas Talbot, Marcus S Noel, Bridget Keenan, Devalingam Mahalingam, Min-Sun Song, Mélanie Grosso, Denis Arnaud, Aurelie Auguste, Dimitris Zacharoulis, Jan Storkholm, Iain McNeish, Robert Habib, John J Rossi, Nagy A Habib
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引用次数: 0

摘要

许多癌症患者不能从目前批准的免疫检查点抑制剂(ICIs)中获益,这表明需要对免疫抑制性肿瘤微环境(TME)进行额外的免疫调节。MTL-CCAAT增强结合蛋白α (CEBPA)特异性上调主髓系转录因子CEBPA的表达,缓解髓系驱动的免疫抑制。在这里,我们报告了MTL-CEBPA联合派姆单抗治疗晚期实体肿瘤患者的安全性、耐受性、药代动力学和疗效,这些肿瘤通常表现为ICI耐药性。配对患者活检的多模式探索性分析显示与MTL-CEBPA和派姆单抗联合治疗相关的生物学变化,包括T细胞和抗原呈递细胞的浸润增加,支持从免疫荒漠向免疫炎症性更强的TME转化。疾病稳定的患者在治疗后表现出免疫抑制髓细胞的减少。总的来说,这些数据支持MTL-CEBPA在减轻TME免疫抑制中的作用。该研究已在ClinicalTrials.gov注册(NCT04105335)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TIMEPOINT, a phase 1 study combining MTL-CEBPA with pembrolizumab, supports the immunomodulatory effect of MTL-CEBPA in solid tumors.

Many patients with cancer do not benefit from currently approved immune checkpoint inhibitors (ICIs), suggesting that additional immunomodulation of the immunosuppressive tumor microenvironment (TME) is required. MTL-CCAAT enhancer-binding protein alpha (CEBPA) specifically upregulates the expression of the master myeloid transcription factor, CEBPA, relieving myeloid-driven immunosuppression. Here, we report the safety, tolerability, pharmacokinetics, and efficacy of MTL-CEBPA in combination with pembrolizumab in patients with advanced solid tumors that typically show ICI resistance. Multimodal exploratory analyses of paired patient biopsies demonstrate biological changes associated with the combination treatment of MTL-CEBPA and pembrolizumab, including increased infiltration of T cell and antigen-presenting cells supporting conversion from an immune-desert toward a more immune-inflamed TME. Patients with disease stabilization demonstrate reductions in immunosuppressive myeloid cells post treatment. Collectively, these data support a role for MTL-CEBPA in reducing immunosuppression in the TME. This study was registered at ClinicalTrials.gov (NCT04105335).

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来源期刊
Cell Reports Medicine
Cell Reports Medicine Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
15.00
自引率
1.40%
发文量
231
审稿时长
40 days
期刊介绍: Cell Reports Medicine is an esteemed open-access journal by Cell Press that publishes groundbreaking research in translational and clinical biomedical sciences, influencing human health and medicine. Our journal ensures wide visibility and accessibility, reaching scientists and clinicians across various medical disciplines. We publish original research that spans from intriguing human biology concepts to all aspects of clinical work. We encourage submissions that introduce innovative ideas, forging new paths in clinical research and practice. We also welcome studies that provide vital information, enhancing our understanding of current standards of care in diagnosis, treatment, and prognosis. This encompasses translational studies, clinical trials (including long-term follow-ups), genomics, biomarker discovery, and technological advancements that contribute to diagnostics, treatment, and healthcare. Additionally, studies based on vertebrate model organisms are within the scope of the journal, as long as they directly relate to human health and disease.
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