Yamaguchi Y, Takayama T, Kawami H, Sato Y, Baba N, Kuroi K, Toge T
Department of Surgery, Hiroshima University, Japan.
Nihon Geka Gakkai Zasshi. 1991 Sep;92(9):1234-6.
Clinical efficacy of lymphokine-activated killer (LAK) cell adoptive immunotherapy (AIT) in combination with plasma exchange and interleukin (IL-2) was investigated in 24 patients with advanced cancer. Partial response (PR) was found in 4 patients (20%), including 1 primary liver tumor, 1 metastatic lung tumor from renal cancer and 2 malignant pleural effusions from gastric and lung cancer. Based on these results new AIT in combination with plasma exchange, OK-432, IL-2 and cyclophosphamide was designed to target liver and lung tumors, in which LAK cells and other drugs were administered through the catheter located in the feeding artery of the tumor. Out of ten patients treated, 1 (10%) with metastatic liver tumor from gallbladder cancer was evaluated as PR. It is suggested that a strategy to enhance tumor accumulation and recognition of LAK cells should be attempted for development of gastrointestinal cancer therapy with AIT.
对24例晚期癌症患者研究了淋巴因子激活的杀伤细胞(LAK)过继性免疫疗法(AIT)联合血浆置换和白细胞介素(IL-2)的临床疗效。4例患者(20%)出现部分缓解(PR),包括1例原发性肝癌、1例肾癌肺转移瘤以及2例胃癌和肺癌所致恶性胸腔积液。基于这些结果,设计了联合血浆置换、溶链菌制剂、IL-2和环磷酰胺的新型AIT来靶向肝脏和肺部肿瘤,其中LAK细胞和其他药物通过位于肿瘤供血动脉的导管给药。在接受治疗的10例患者中,1例胆囊癌肝转移瘤患者(10%)被评估为PR。提示应尝试增强LAK细胞肿瘤蓄积和识别的策略,以开发AIT用于胃肠道癌治疗。