Rosenberg Steven A, Dudley Mark E
Surgery Branch, National Cancer Institute, NIH, Bethesda, MD, USA.
Curr Opin Immunol. 2009 Apr;21(2):233-40. doi: 10.1016/j.coi.2009.03.002. Epub 2009 Mar 21.
Adoptive cell therapy (ACT) is the best available treatment for patients with metastatic melanoma. In a recent series of three consecutive clinical trials using increasing lymphodepletion before infusion of autologous tumor infiltrating lymphocytes (TIL), objective response rates between 49% and 72% were seen. Persistence of infused cells in the circulation at one month was highly correlated with anti-tumor response as was the mean telomere length of the cells infused and the number of CD8+ CD27+ cells infused. Responses occur at all sites and appear to be durable with many patients in ongoing response beyond three years. In the most recent trial of 25 patients receiving maximum lymphodepletion, seven of the 25 patients (28%) achieved a complete response. Of the 12 patients in the three trials who achieved a complete response all but one are ongoing between 18 and 75 months. We recently demonstrated that ACT using autologous lymphocytes genetically modified to express anti-tumor T cell receptors can mediate tumor regression and this approach is now being applied to patients with common epithelial cancers.
过继性细胞疗法(ACT)是转移性黑色素瘤患者可采用的最佳治疗方法。在最近一系列连续三项临床试验中,在输注自体肿瘤浸润淋巴细胞(TIL)之前使用了强度递增的淋巴细胞清除疗法,客观缓解率为49%至72%。输注的细胞在循环系统中一个月后的持续存在情况与抗肿瘤反应高度相关,输注细胞的平均端粒长度和输注的CD8+CD27+细胞数量也与抗肿瘤反应高度相关。所有部位均出现反应,且似乎具有持久性,许多患者的持续反应超过三年。在最近一项针对25名接受最大程度淋巴细胞清除疗法的患者的试验中,25名患者中有7名(28%)实现了完全缓解。在这三项试验中实现完全缓解的12名患者中,除一人外,其余患者的持续缓解时间为18至75个月。我们最近证明,使用经基因改造以表达抗肿瘤T细胞受体的自体淋巴细胞进行ACT可介导肿瘤消退,目前这种方法正在应用于常见上皮癌患者。