Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Ishikawa, Japan; Department of Immunology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Ishikawa, Japan.
Gastroenterology. 2017 May;152(6):1395-1406.e10. doi: 10.1053/j.gastro.2017.02.001. Epub 2017 Feb 7.
BACKGROUND & AIMS: Levels of α-fetoprotein (AFP) are measured for surveillance and diagnosis of hepatocellular carcinoma (HCC). We performed a phase 1 trial to evaluate the safety and efficacy of AFP-derived peptides as an anti-tumor vaccine for patients with advanced HCC, and characterized induction of AFP-specific T-cell receptors (TCRs).
We performed a prospective study of 15 patients with HCC seen at Kanazawa University Hospital in Japan from March 2010 through March 2012. Each patient was given a subcutaneous injection of 3 mg AFP-derived peptides (AFP and AFP) in an emulsion with incomplete Freund's adjuvant every other week for at least 6 weeks. Patients were evaluated every 8 weeks by radiologic imaging; adverse events and toxicities were categorized and graded using the common terminology criteria for adverse events. Criteria for discontinuation included unacceptable toxicities and disease progression defined as progressive disease using the Response Evaluation Criteria In Solid Tumors criteria. Patients' immune responses were monitored using an interferon-gamma enzyme-linked immunospot assay. Peptide-specific TCRs were assessed using a rapid TCR cloning and evaluation system. The observation period was 730 days. A complete response was defined as the disappearance of all tumors; stable disease was defined as tumors whose total diameter remained between >70% and <120% of the baseline measurement, without new lesions.
We did not observe any serious adverse reactions to the peptides, which were well tolerated. Of the 15 patients who received at least 3 injections, 5 (33%) had an immune response to the peptides. One of the 15 patients had a complete response and disease stabilized in 8 patients. In 4 of the 15 patients, we detected AFP-specific CD8 T cells; we cloned 14 different TCRs with different avidities for the peptide. A TCR with the highest avidity was observed in the patient who achieved a complete response for more than 2 years.
In a phase 1 trial, administration of AFP-derived peptides to 15 patients with HCC did not cause adverse events and produced T cells with receptors that reacted to the peptides; 1 patient had a complete response and tumor growth slowed in 8 patients. T cells from the patient with a complete response expressed a highly functional TCR induced by the peptide vaccines. UMIN-CTR no: UMIN000003514.
甲胎蛋白(AFP)水平用于监测和诊断肝细胞癌(HCC)。我们进行了一项 1 期试验,以评估 AFP 衍生肽作为晚期 HCC 患者抗肿瘤疫苗的安全性和有效性,并对 AFP 特异性 T 细胞受体(TCR)的诱导进行了特征描述。
我们对 2010 年 3 月至 2012 年 3 月在日本金泽大学医院就诊的 15 例 HCC 患者进行了前瞻性研究。每位患者每两周皮下注射 3 毫克 AFP 衍生肽(AFP 和 AFP)在不完全弗氏佐剂乳剂中,至少 6 周。每 8 周通过影像学评估患者;使用不良事件常用术语标准对不良事件和毒性进行分类和分级。停药标准包括不可接受的毒性和疾病进展,使用实体瘤反应评价标准定义为疾病进展。使用干扰素-γ酶联免疫斑点测定法监测患者的免疫反应。使用快速 TCR 克隆和评估系统评估肽特异性 TCR。观察期为 730 天。完全缓解定义为所有肿瘤消失;稳定疾病定义为肿瘤总直径保持在基线测量值的>70%至<120%之间,无新病变。
我们没有观察到肽的任何严重不良反应,患者耐受性良好。在至少接受 3 次注射的 15 名患者中,有 5 名(33%)对肽有免疫反应。15 名患者中有 1 名完全缓解,8 名患者病情稳定。在 15 名患者中的 4 名中,我们检测到 AFP 特异性 CD8 T 细胞;我们克隆了 14 种不同亲和力的肽 TCR。在一名完全缓解超过 2 年的患者中观察到具有最高亲和力的 TCR。
在 1 期试验中,向 15 例 HCC 患者给予 AFP 衍生肽不会引起不良反应,并产生能与肽反应的受体的 T 细胞;1 例患者完全缓解,8 例患者肿瘤生长速度减慢。完全缓解患者的 T 细胞表达由肽疫苗诱导的高功能 TCR。UMIN-CTR 编号:UMIN000003514。