Roman M. Shapiro, Michal Sheffer, Matthew A. Booker, Michael Y. Tolstorukov, Grace C. Birch, Moshe Sade-Feldman, Jacy Fang, Shuqiang Li, Wesley Lu, Michela Ansuinelli, Remy Dulery, Mubin Tarannum, Joanna Baginska, Nishant Dwivedi, Ashish Kothari, Livius Penter, Yasmin Z. Abdulhamid, Isabel E. Kaplan, Dinh Khanhlinh, Ravindra Uppaluri, Robert A. Redd, Sarah Nikiforow, John Koreth, Jerome Ritz, Catherine J. Wu, Robert J. Soiffer, glenn hanna, Rizwan Romee
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引用次数: 0
摘要
细胞因子诱导的记忆样自然杀伤(CIML NK)细胞与IL-15超级拮抗剂(N-803)相结合是治疗复发/难治性头颈癌的一种新方法。我们报告了单倍体CIML NK细胞联合N-803与或不联合伊匹单抗(IPI)治疗复发/难治性头颈癌患者的I期试验数据。研究的主要终点是安全性,1/10的患者出现了剂量限制性毒性。70%的短暂疾病控制率与供体NK细胞扩增有关,后者与IPI无关。高分辨率免疫表型和转录谱分析确定了体内 NK 细胞及其相互作用伙伴的特征。IPI与Treg:Tcon的收缩、受体CD8+ T细胞的快速恢复以及供体NK细胞的加速排斥有关。这些结果为评估晚期恶性肿瘤的CIML NK疗法提供了参考,并考虑了与IPI的结合。
First-in-human evaluation of memory-like NK cells with an IL-15 super-agonist and CTLA-4 blockade in advanced head and neck cancer
Cytokine induced memory-like natural killer (CIML NK) cells combined with an IL-15 super-agonist (N-803) are a novel modality to treat relapsed/refractory head and neck cancer. We report data from a phase I trial of haploidentical CIML NK cells combined with N-803 with or without ipilimumab (IPI) in relapsed/refractory head and neck cancer patients after a median of 6 prior lines of therapy. The primary endpoint was safety, which was established, with dose-limiting toxicity in 1/10 patients. A promising though transient disease control rate of 70% correlated with donor NK cell expansion, the latter occurring irrespective of IPI. High-resolution immunophenotypic and transcriptional profiling characterized the NK cells and their interacting partners in vivo. IPI was associated with contraction of Treg:Tcon, rapid recovery of recipient CD8+ T cells, and accelerated rejection of donor NK cells. These results inform evaluation of CIML NK therapy for advanced malignancies, with considerations for combination with IPI.