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术前 CTLA-4 阻断:术前临床试验中耐受性和免疫监测。

Preoperative CTLA-4 blockade: tolerability and immune monitoring in the setting of a presurgical clinical trial.

机构信息

Department of Genitourinary Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Clin Cancer Res. 2010 May 15;16(10):2861-71. doi: 10.1158/1078-0432.CCR-10-0569. Epub 2010 May 11.

Abstract

PURPOSE

Cytotoxic T lymphocyte associated antigen (CTLA-4) blockade is being explored in numerous clinical trials as an immune-based therapy for different malignancies. Our group conducted the first preoperative clinical trial with the anti-CTLA-4 antibody ipilimumab in 12 patients with localized urothelial carcinoma of the bladder.

EXPERIMENTAL DESIGN

Six patients were treated with 3 mg/kg/dose of anti-CTLA-4 and six patients were treated with 10 mg/kg/dose of antibody. Primary end points of the study were safety and immune monitoring.

RESULTS

Most drug-related adverse events consisted of grade 1/2 toxicities. All patients had measurable immunologic pharmacodynamic effects, consisting of an increased frequency of CD4+ICOShi T cells in tumor tissues and the systemic circulation. To determine if CD4+ICOShi T cells could be a correlative marker for clinical outcome after treatment with anti-CTLA-4, a cohort of metastatic melanoma patients was studied retrospectively for frequency of CD4+ICOShi T cells and survival. Data from this small cohort of patients indicated that an increased frequency of CD4+ICOShi T cells, sustained over a period of 12 weeks of therapy, correlates with increased likelihood of clinical benefit consisting of overall survival.

CONCLUSIONS

Our trial shows that anti-CTLA-4 therapy has a tolerable safety profile in the presurgical setting and that a preoperative model can be used to obtain biological data on human immune responses, which can efficiently guide the monitoring of patients treated in the metastatic disease setting.

摘要

目的

细胞毒性 T 淋巴细胞相关抗原(CTLA-4)阻断正在许多临床试验中作为一种针对不同恶性肿瘤的免疫治疗方法进行探索。我们的团队在 12 例局部膀胱癌患者中首次进行了抗 CTLA-4 抗体 ipilimumab 的术前临床试验。

实验设计

6 例患者接受 3mg/kg/d 剂量的抗 CTLA-4 治疗,6 例患者接受 10mg/kg/d 剂量的抗体治疗。该研究的主要终点是安全性和免疫监测。

结果

大多数药物相关不良事件均为 1/2 级毒性。所有患者均具有可测量的免疫药效学效应,包括肿瘤组织和全身循环中 CD4+ICOShi T 细胞的频率增加。为了确定 CD4+ICOShi T 细胞是否可以作为抗 CTLA-4 治疗后临床结果的相关标志物,我们回顾性研究了一组转移性黑色素瘤患者 CD4+ICOShi T 细胞的频率和生存情况。该小队列患者的数据表明,在 12 周的治疗期间持续增加 CD4+ICOShi T 细胞的频率与总生存率增加的临床获益相关。

结论

我们的试验表明,抗 CTLA-4 治疗在术前环境中具有可耐受的安全性,并且术前模型可用于获得人类免疫反应的生物学数据,这可以有效地指导转移性疾病患者的监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c75/2919850/d515365be093/nihms193847f1.jpg

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