Barba D, Saris S C, Holder C, Rosenberg S A, Oldfield E H
Clinical Neurosurgery Section, National Institute of Neurological and Communicative Disorders and Stroke, Bethesda, Maryland.
J Neurosurg. 1989 Feb;70(2):175-82. doi: 10.3171/jns.1989.70.2.0175.
Adoptive immunotherapy using lymphokine-activated killer (LAK) cells and interleukin-2 (IL-2) offers the possibility of a new treatment for patients with malignant glial tumors. In a clinical trial, the effectiveness of a 5-day treatment cycle of direct intratumoral administration of both LAK cells and IL-2 via a reservoir/catheter system in patients with recurrent malignant gliomas was studied. Ten patients were entered into the study, nine of whom were treated with 15 cycles of LAK cells (0.9 to 21.0 x 10(9) cells) and IL-2 (49 to 450 x 10(3) U/kg). The 10th patient in the study was not treated because of the onset of severe neurological deficits prior to beginning immunotherapy. Of the nine patients treated, one had a partial tumor response to immunotherapy as documented by computerized tomography. Neurological side effects occurred in all patients undergoing treatment and were related to increases in cerebral edema that appeared to be mediated by the immunotherapy. This report demonstrates the present limitations of regional adoptive immunotherapy with LAK cells and IL-2 in the treatment of human glial tumors.
采用淋巴因子激活的杀伤细胞(LAK)和白细胞介素-2(IL-2)进行过继性免疫治疗为恶性胶质瘤患者提供了一种新的治疗可能性。在一项临床试验中,研究了通过储液器/导管系统对复发性恶性胶质瘤患者直接瘤内注射LAK细胞和IL-2的5天治疗周期的有效性。10名患者进入该研究,其中9名接受了15个周期的LAK细胞(0.9至21.0×10⁹个细胞)和IL-2(49至450×10³U/kg)治疗。研究中的第10名患者因在免疫治疗开始前出现严重神经功能缺损而未接受治疗。在接受治疗的9名患者中,有1名经计算机断层扫描记录显示对免疫治疗有部分肿瘤反应。所有接受治疗的患者均出现神经学副作用,且与免疫治疗介导的脑水肿增加有关。本报告证明了目前LAK细胞和IL-2区域过继性免疫治疗在治疗人类胶质瘤方面的局限性。