Copier J, Dalgleish A G, Britten C M, Finke L H, Gaudernack G, Gnjatic S, Kallen K, Kiessling R, Schuessler-Lenz M, Singh H, Talmadge J, Zwierzina H, Håkansson L
Cellular and Molecular Medicine, St. George's University of London, London, UK.
Eur J Cancer. 2009 May;45(8):1424-31. doi: 10.1016/j.ejca.2008.12.017. Epub 2009 Jan 21.
A series of cancer vaccines have been evaluated in clinical trials with encouraging results, but the demonstration of clinical benefit in confirmatory studies has so far proven to be difficult. The development of cancer vaccines is hampered by a range of issues particular to this field of research. On 12th March 2008, the Biotherapy Development Association convened a workshop to discuss issues faced by scientists and clinicians involved in the development of cancer vaccines. This paper is a review of the field, based on discussions held at the BDA workshop, and describes biological barriers encountered in generating effective immune responses to tumours, methodological obstacles encountered in the improvement of immunological monitoring which aims to improve inter-laboratory and inter-trial comparisons, challenges in clinical trial design and problems posed by the lack of specific regulation for cancer vaccines and the impact on their development. Ultimately, a number of general solutions are posed: (1) better patient selection, (2) use of multi-modal treatments that affect several aspects of the immune system at once, (3) a requirement for the development of good biomarkers to stratify patients for selection prior to trial and as surrogates for clinical response and (4) harmonisation of SOPs for immunological monitoring of clinical trials.
一系列癌症疫苗已在临床试验中进行了评估,结果令人鼓舞,但迄今为止,在验证性研究中证明其临床益处却很困难。癌症疫苗的研发受到该研究领域一系列特殊问题的阻碍。2008年3月12日,生物治疗发展协会召开了一次研讨会,讨论参与癌症疫苗研发的科学家和临床医生所面临的问题。本文基于生物治疗发展协会研讨会上的讨论,对该领域进行了综述,描述了在产生针对肿瘤的有效免疫反应过程中遇到的生物学障碍、旨在改善实验室间和试验间比较的免疫监测改进中遇到的方法学障碍、临床试验设计中的挑战以及癌症疫苗缺乏特定监管所带来的问题及其对疫苗研发的影响。最终,提出了一些通用解决方案:(1)更好地选择患者;(2)使用能同时影响免疫系统多个方面的多模式治疗方法;(3)要求开发良好的生物标志物,以便在试验前对患者进行分层选择,并作为临床反应的替代指标;(4)统一临床试验免疫监测的标准操作规程。