Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Cellular Therapeutics Center, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Cancer Discov. 2021 Nov;11(11):2748-2763. doi: 10.1158/2159-8290.CD-21-0407. Epub 2021 Jul 15.
Malignant pleural diseases, comprising metastatic lung and breast cancers and malignant pleural mesothelioma (MPM), are aggressive solid tumors with poor therapeutic response. We developed and conducted a first-in-human, phase I study of regionally delivered, autologous, mesothelin-targeted chimeric antigen receptor (CAR) T-cell therapy. Intrapleural administration of 0.3M to 60M CAR T cells/kg in 27 patients (25 with MPM) was safe and well tolerated. CAR T cells were detected in peripheral blood for >100 days in 39% of patients. Following our demonstration that PD-1 blockade enhances CAR T-cell function in mice, 18 patients with MPM also received pembrolizumab safely. Among those patients, median overall survival from CAR T-cell infusion was 23.9 months (1-year overall survival, 83%). Stable disease was sustained for ≥6 months in 8 patients; 2 exhibited complete metabolic response on PET scan. Combination immunotherapy with CAR T cells and PD-1 blockade agents should be further evaluated in patients with solid tumors. SIGNIFICANCE: Regional delivery of mesothelin-targeted CAR T-cell therapy followed by pembrolizumab administration is feasible, safe, and demonstrates evidence of antitumor efficacy in patients with malignant pleural diseases. Our data support the investigation of combination immunotherapy with CAR T cells and PD-1 blockade agents in solid tumors...
恶性胸膜疾病包括转移性肺癌和乳腺癌以及恶性胸膜间皮瘤(MPM),是具有不良治疗反应的侵袭性实体肿瘤。我们开发并进行了首例人体、I 期研究,研究局部递送电针对间皮素的嵌合抗原受体(CAR)T 细胞疗法。27 名患者(25 名患有 MPM)接受了 0.3M 至 60M CAR T 细胞/kg 的胸腔内给药,安全性和耐受性良好。39%的患者外周血中可检测到 CAR T 细胞>100 天。在我们证明 PD-1 阻断剂增强了小鼠中 CAR T 细胞的功能之后,18 名 MPM 患者也安全地接受了 pembrolizumab 治疗。在这些患者中,从 CAR T 细胞输注开始的中位总生存期为 23.9 个月(1 年总生存率为 83%)。8 名患者的疾病稳定持续≥6 个月;2 名患者在 PET 扫描上表现出完全代谢反应。CAR T 细胞和 PD-1 阻断剂联合免疫疗法应在实体瘤患者中进一步评估。意义:间皮素靶向 CAR T 细胞疗法的局部递送,随后进行 pembrolizumab 给药,在恶性胸膜疾病患者中是可行的、安全的,并显示出抗肿瘤疗效的证据。我们的数据支持在实体瘤中进行 CAR T 细胞和 PD-1 阻断剂联合免疫疗法的研究。