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粒细胞巨噬细胞集落刺激因子与自体肿瘤疫苗对肾细胞癌患者的免疫作用

Immunological effects of granulocyte-macrophage colony-stimulating factor and autologous tumor vaccine in patients with renal cell carcinoma.

作者信息

Schwaab Thomas, Tretter Christopher P, Gibson Jennifer J, Cole Bernard F, Schned Alan R, Harris Robert, Wallen Eric M, Fisher Jan L, Waugh Mary G, Truman Debra, Stempkowski Laura M, Crosby Nancy A, Heaney John A, Ernstoff Marc S

机构信息

Uro-Oncology Group, Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire 03756-0001, USA.

出版信息

J Urol. 2004 Mar;171(3):1036-42. doi: 10.1097/01.ju.0000113275.91953.5d.

Abstract

PURPOSE

Biological therapy for renal cell carcinoma (RCC) uses agents that mobilize immune effector cells which are able to recognize and destroy cancer. We evaluated the effects of weekly then monthly autologous tumor vaccine combined with daily granulocyte macrophage-colony stimulating factor (GM-CSF) in patients with RCC as a method of stimulating antigen presenting cells.

MATERIALS AND METHODS

Eligible patients with pathological stage II to IV RCC were entered into this pilot study. Autologous tumor vaccine (0.5 to 1 x 107 irradiated tumor cells) admixed with 250 microg GM-CSF per vaccine was given subcutaneously weekly for 4 weeks and then monthly for 4 months. GM-CSF (125 microg/m2) was given subcutaneously for 13 days after vaccine injection 1 and injections 4 to 8. Treatment related tumor specific CD4 and CD8 positive T cell precursors were assessed.

RESULTS

A total of 22 patients were entered into this study. Patients were stratified by bulk of disease (group 1, 9 patients with micrometastatic disease, and group 2, 13 patients with macrometastatic disease). In general treatment was well tolerated. Of 9 patients in group 1 7 remained disease-free after nephrectomy. In group 2, 6 patients had stable (46.2%) and 7 patients had progressive disease (53.8%). Statistically significant treatment related increases in CD4 (p = 0.028) and CD8 (p = 0.018) positive tumor specific T cell precursors were observed for the entire group of patients. Changes in CD4 and CD8 positive precursors correlated significantly with each other (p = 0.0001). This correlation was seen in the 2 patient subpopulations as well (group 1 p = 0.003, group 2 p = 0.013). Patients with minimal disease, and with changes in CD4 and CD8 positive tumor specific T cell precursors greater than the median appeared to have an improved time to progression as well as a survival benefit.

CONCLUSIONS

GM-CSF and autologous vaccine can be given safely in combination to patients with renal cell cancer. We observed treatment related changes in tumor specific circulating lymphocyte populations.

摘要

目的

肾细胞癌(RCC)的生物治疗使用能动员免疫效应细胞的药物,这些细胞能够识别并摧毁癌细胞。我们评估了每周一次随后每月一次的自体肿瘤疫苗联合每日使用粒细胞巨噬细胞集落刺激因子(GM-CSF)对肾细胞癌患者的疗效,以此作为刺激抗原呈递细胞的一种方法。

材料与方法

符合条件的病理分期为II至IV期的肾细胞癌患者进入该初步研究。自体肿瘤疫苗(0.5至1×10⁷经照射的肿瘤细胞)与每剂疫苗250微克GM-CSF混合,每周皮下注射一次,共4周,然后每月注射一次,共4个月。在第1次疫苗注射以及第4至8次注射后,GM-CSF(125微克/平方米)皮下注射13天。评估与治疗相关的肿瘤特异性CD4和CD8阳性T细胞前体。

结果

共有22名患者进入本研究。患者按疾病负荷分层(第1组,9名微转移疾病患者;第2组,13名大转移疾病患者)。总体而言,治疗耐受性良好。第1组的9名患者中,7名在肾切除术后无疾病进展。在第2组中,6名患者病情稳定(46.2%),7名患者病情进展(53.8%)。在整个患者组中观察到与治疗相关的CD4(p = 0.028)和CD8(p = 0.018)阳性肿瘤特异性T细胞前体有统计学意义的增加。CD4和CD8阳性前体的变化彼此显著相关(p = 0.0001)。在两个患者亚组中也观察到这种相关性(第1组p = 0.003,第2组p = 0.013)。疾病程度较轻且CD4和CD8阳性肿瘤特异性T细胞前体变化大于中位数的患者似乎有更长的疾病进展时间以及生存获益。

结论

GM-CSF和自体疫苗联合应用于肾细胞癌患者可安全给药。我们观察到了与治疗相关的肿瘤特异性循环淋巴细胞群体的变化。

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