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E75 肽疫苗在乳腺癌患者中的应用:系统评价和荟萃分析。

Application of E75 peptide vaccine in breast cancer patients: A systematic review and meta-analysis.

机构信息

Cancer Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Cancer Research Center, Tehran University of Medical Sciences, Tehran, Iran; Breast Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Eur J Pharmacol. 2018 Jul 15;831:87-93. doi: 10.1016/j.ejphar.2018.05.010. Epub 2018 May 9.

Abstract

The E75 peptide vaccine, derived from tumor-associated antigen HER2, is the most frequently studied anti-HER2 vaccination strategy for the treatment of breast cancer patients. It has been investigated in the several phases Ι/Π of the clinical trials and is currently being evaluated in a randomized multicenter phase III clinical trial. We conducted a systematic review and meta-analysis to clarify the outcomes of the E75 peptide vaccine including the therapeutic efficacy, the disease recurrence, the survival rate, and the side effects. Three peer-reviewed literature databases including the PubMed, Web of Science, and Scopus were sought. Of 29 trials assessed for eligibility, 16 were considered based on our inclusion criteria. Statistical analyses were performed by The Excel and STATA v.11.0. Meta-analysis of delayed-type hypersensitivity)DTH( reactions and CD8-T cell levels, as immune responses, displayed the significant differences in the vaccinated groups compared to their non-vaccinated counterparts. In addition, the recurrence, and the overall and the disease-free survival were significantly different in the vaccinated subjects versus the control. Evaluation of the local and systemic toxicity of the E75 peptide vaccine demonstrated the minimal side effects. It seems that the E75 peptide vaccine is safe and effective, and can be used for further randomized clinical trials.

摘要

E75 肽疫苗来源于肿瘤相关抗原 HER2,是目前研究最多的针对乳腺癌患者的抗 HER2 疫苗接种策略。它已经在几期Ⅰ/Ⅱ临床试验中进行了研究,目前正在一项随机、多中心的 III 期临床试验中进行评估。我们进行了一项系统评价和荟萃分析,以明确 E75 肽疫苗的结果,包括治疗效果、疾病复发、生存率和副作用。我们在三个同行评议的文献数据库(PubMed、Web of Science 和 Scopus)中进行了搜索。在评估的 29 项试验中,有 16 项符合我们的纳入标准。使用 Excel 和 STATA v.11.0 进行了统计分析。作为免疫反应的迟发型超敏反应(DTH)反应和 CD8-T 细胞水平的荟萃分析显示,接种组与未接种组相比存在显著差异。此外,接种组的复发率、总生存率和无病生存率与对照组相比也存在显著差异。对 E75 肽疫苗的局部和全身毒性的评估表明,其副作用极小。E75 肽疫苗似乎是安全有效的,可以用于进一步的随机临床试验。

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