Research and Development Division, Tella Inc, Tokyo, Japan.
Pancreas. 2012 Mar;41(2):195-205. doi: 10.1097/MPA.0b013e31822398c6.
In the current study, we have evaluated the clinical and immunological responses in patients with advanced pancreatic carcinoma who received dendritic cell (DC)-based immunotherapy in combination with gemcitabine and/or S-1.
Dendritic cell-based immunotherapy (DC vaccine alone or DC vaccine plus lymphokine-activated killer [LAK] cell therapy) in combination with gemcitabine and/or S-1 has been carried out in 49 patients with inoperable pancreatic carcinoma refractory to standard treatment.
Of 49 patients, 2 patients had complete remission, 5 had partial remission, and 10 had stable disease. Prolongation of survival in this cohort was highly likely (median survival, 360 days). Survival of patients receiving DC vaccine and chemotherapy plus LAK cell therapy was longer than those receiving DC vaccine in combination with chemotherapy but no LAK cells. Increased numbers of cancer antigen-specific cytotoxic T cells and decreased regulatory T cells were observed in several patients on immunotherapy, but increased overall survival time tended to be associated only with the latter. None of the patients experienced grade 3 or worse adverse events during the treatment period.
Dendritic cell vaccine-based immunotherapy combined with chemotherapy was shown to be safe and possibly effective in patients with advanced pancreatic cancer refractory to standard treatment.
在本研究中,我们评估了接受基于树突状细胞(DC)的免疫疗法联合吉西他滨和/或 S-1 治疗的晚期胰腺癌患者的临床和免疫反应。
对 49 例无法手术的对标准治疗耐药的胰腺癌患者进行了基于树突状细胞的免疫疗法(单独使用 DC 疫苗或 DC 疫苗加淋巴因子激活的杀伤[LAK]细胞疗法)联合吉西他滨和/或 S-1。
49 例患者中,2 例完全缓解,5 例部分缓解,10 例病情稳定。该队列的生存期延长的可能性很高(中位生存期为 360 天)。接受 DC 疫苗和化疗加 LAK 细胞治疗的患者的生存时间长于接受 DC 疫苗联合化疗但无 LAK 细胞的患者。在接受免疫治疗的一些患者中观察到癌症抗原特异性细胞毒性 T 细胞数量增加和调节性 T 细胞减少,但总生存时间的延长似乎仅与后者相关。在治疗期间,没有患者出现 3 级或更高级别的不良事件。
对于对标准治疗耐药的晚期胰腺癌患者,基于树突状细胞疫苗的免疫疗法联合化疗显示出安全性和有效性。