Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany
Zellwerk GmbH, Oberkrämer, Germany.
J Immunother Cancer. 2023 Jan;11(1). doi: 10.1136/jitc-2022-005847.
Adoptive transfer of autologous tumor-specific lymphocytes represents a viable treatment method for patients with advanced malignancies. Here, we report a patient's case with metastatic hormone-refractory New York esophageal squamous cell carcinoma 1 (NY-ESO-1) expressing prostate cancer treated with in vitro expanded tumor-infiltrating lymphocytes (TILs) in conjunction with IL-2 and immune-checkpoint blockade. Complete and durable tumor remission was observed after three TIL infusions consisting of 1.4×10, 2.0×10, and 8.0×10 T cells, respectively, lasting now for more than 3.5 years. Immunological correlates to the clinical development were the decrease of tumor-driven NY-ESO-1 serum antibody and the drop of prostate-specific antigen to <0.01 µg/L. TILs were reactive against cancer-testis antigen NY-ESO-1, individual tumor mutational proteins (eg, PRPF8, TRPS1), and the androgen receptor splice variant 12.
过继输注自体肿瘤特异性淋巴细胞是治疗晚期恶性肿瘤患者的一种可行方法。在这里,我们报告了一例转移性激素难治性纽约食管鳞状细胞癌 1(NY-ESO-1)表达的前列腺癌患者,该患者接受了体外扩增的肿瘤浸润淋巴细胞(TIL)联合白细胞介素 2(IL-2)和免疫检查点阻断治疗。在三次 TIL 输注后观察到完全和持久的肿瘤消退,每次输注的 TIL 分别为 1.4×10、2.0×10 和 8.0×10,持续时间超过 3.5 年。与临床发展相关的免疫相关性是肿瘤驱动的 NY-ESO-1 血清抗体减少和前列腺特异性抗原降至<0.01μg/L。TIL 对癌症睾丸抗原 NY-ESO-1、个体肿瘤突变蛋白(如 PRPF8、TRPS1)和雄激素受体剪接变体 12 有反应。