O'Rourke Donald M, Nasrallah MacLean P, Desai Arati, Melenhorst Jan J, Mansfield Keith, Morrissette Jennifer J D, Martinez-Lage Maria, Brem Steven, Maloney Eileen, Shen Angela, Isaacs Randi, Mohan Suyash, Plesa Gabriela, Lacey Simon F, Navenot Jean-Marc, Zheng Zhaohui, Levine Bruce L, Okada Hideho, June Carl H, Brogdon Jennifer L, Maus Marcela V
Department of Neurosurgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Division of Neuropathology, Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Sci Transl Med. 2017 Jul 19;9(399). doi: 10.1126/scitranslmed.aaa0984.
We conducted a first-in-human study of intravenous delivery of a single dose of autologous T cells redirected to the epidermal growth factor receptor variant III (EGFRvIII) mutation by a chimeric antigen receptor (CAR). We report our findings on the first 10 recurrent glioblastoma (GBM) patients treated. We found that manufacturing and infusion of CAR-modified T cell (CART)-EGFRvIII cells are feasible and safe, without evidence of off-tumor toxicity or cytokine release syndrome. One patient has had residual stable disease for over 18 months of follow-up. All patients demonstrated detectable transient expansion of CART-EGFRvIII cells in peripheral blood. Seven patients had post-CART-EGFRvIII surgical intervention, which allowed for tissue-specific analysis of CART-EGFRvIII trafficking to the tumor, phenotyping of tumor-infiltrating T cells and the tumor microenvironment in situ, and analysis of post-therapy EGFRvIII target antigen expression. Imaging findings after CART immunotherapy were complex to interpret, further reinforcing the need for pathologic sampling in infused patients. We found trafficking of CART-EGFRvIII cells to regions of active GBM, with antigen decrease in five of these seven patients. In situ evaluation of the tumor environment demonstrated increased and robust expression of inhibitory molecules and infiltration by regulatory T cells after CART-EGFRvIII infusion, compared to pre-CART-EGFRvIII infusion tumor specimens. Our initial experience with CAR T cells in recurrent GBM suggests that although intravenous infusion results in on-target activity in the brain, overcoming the adaptive changes in the local tumor microenvironment and addressing the antigen heterogeneity may improve the efficacy of EGFRvIII-directed strategies in GBM.
我们开展了一项针对通过嵌合抗原受体(CAR)重定向至表皮生长因子受体变异体III(EGFRvIII)突变的单剂量自体T细胞进行静脉输注的首次人体研究。我们报告了对首批10例复发性胶质母细胞瘤(GBM)患者的治疗结果。我们发现,制造和输注CAR修饰的T细胞(CART)-EGFRvIII细胞是可行且安全的,没有证据表明存在肿瘤外毒性或细胞因子释放综合征。一名患者在超过18个月的随访中病情稳定。所有患者外周血中均可检测到CART-EGFRvIII细胞的短暂扩增。7例患者在接受CART-EGFRvIII治疗后接受了手术干预,这使得能够对CART-EGFRvIII向肿瘤的转运、肿瘤浸润性T细胞的表型分析以及原位肿瘤微环境进行组织特异性分析,并对治疗后EGFRvIII靶抗原表达进行分析。CART免疫治疗后的影像学结果难以解释,这进一步凸显了对输注患者进行病理采样的必要性。我们发现CART-EGFRvIII细胞转运至活跃GBM区域,这7例患者中有5例抗原减少。与输注CART-EGFRvIII前的肿瘤标本相比,对肿瘤微环境的原位评估显示,输注CART-EGFRvIII后抑制性分子的表达增加且增强,调节性T细胞浸润增加。我们在复发性GBM中使用CAR T细胞的初步经验表明,尽管静脉输注可在大脑中产生靶向活性,但克服局部肿瘤微环境的适应性变化并解决抗原异质性问题可能会提高EGFRvIII导向策略在GBM中的疗效。