针对神经母细胞瘤的DNA疫苗接种试点临床试验:研究设计和初步结果

Q4 Medicine
I. Proleskovskaya, A. Meleshko, E. Vashkevich, N. E. Konoplya
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引用次数: 0

摘要

简介我们报告了一项针对神经母细胞瘤患者的治疗性DNA疫苗接种试验性临床试验(NCT04049864)的初步结果。文章总结了6名完成疫苗接种的患者的结果。界定了患者的纳入和排除标准。临床方案包括疫苗形式和剂量、定时接种方案和伴随治疗。通过聚合酶链式反应定量分析了所有患者的最小残留病灶,通过ELISpot检测了T细胞免疫反应,通过ELISA检测了反义反应。患者对疫苗的耐受性良好,不良症状极少。在每个疫苗接种疗程两周后对 T 细胞免疫反应进行评估,6 名患者中有 5 人呈阳性反应。1名患者检测到了反义免疫反应。截至 2022 年 1 月 11 日,6 名患者中有 5 人存活并得到临床缓解。接种疫苗患者的无事件生存率为 82 ± 18 %,对照组为 29 ± 11 %(P = 0.03)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pilot clinical trial of DNA vaccination against neuroblastoma: study design and preliminary results
Introduction. We report preliminary results of a pilot clinical trial of therapeutic DNA vaccination of patients with neuroblastoma (NCT04049864).The aim of the study – is to test the safety and immunogenicity of DNA vaccination against neuroblastoma.Materials and methods. The results of 6 patients who completed vaccination are summarized in the article. Inclusion and exclusion criteria for patients are defined. The clinical protocol included vaccine form and doses, timed vaccination regimen, and concomitant therapy. Minimal residual disease was analyzed for all patients by quantitative polymerase chain reaction, measurement of T-cell immune response by ELISpot and antisense response by ELISA.Results. The vaccine was well tolerated by patients with minimal adverse symptoms. T-cell immune response was evaluated two weeks after each course of vaccination and was positive in 5 of 6 patients. An antisense immune response was detected in 1 patient. 5 out of 6 patients are alive and in clinical remission as of 11/01/2022. Event-free survival of vaccinated patients was 82 ± 18 % vs 29 ± 11 % of controls (p = 0.03).
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来源期刊
Russian Journal of Pediatric Hematology and Oncology
Russian Journal of Pediatric Hematology and Oncology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
36
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