Department of Haematology, Hammersmith Hospital, Imperial College, London, UK.
Drugs. 2011 Sep 10;71(13):1659-74. doi: 10.2165/11593270-000000000-00000.
The successful identification of a range of leukaemia-specific and lymphoma-specific antigens in recent years has stimulated efforts to develop therapeutic vaccination strategies. A number of clinical trials have established the safety and immunogenicity of vaccination against tumour antigens, although there are limited data on the clinical efficacy of this approach in haematological malignancies. After encouraging results of phase I/II trials using idiotype vaccines in lymphoma, the outcome of the three phase III trials has been somewhat disappointing. Several other promising strategies are currently being developed to improve these results, including optimization of antigen delivery. In myeloid leukaemias, clinical trials of vaccination with peptides derived from a number of leukaemia antigens, including WT1, PR1, RHAMM and BCR-ABL, have shown evidence of immunogenicity, but limited data are available on the clinical efficacy of this approach. In this review, we focus on the results of clinical trials of vaccination in leukaemia and lymphoma, and discuss potential strategies to enhance the efficacy of immunotherapy in the future.
近年来,成功鉴定了一系列白血病特异性和淋巴瘤特异性抗原,这激发了开发治疗性疫苗策略的努力。多项临床试验已经证实了针对肿瘤抗原的疫苗接种的安全性和免疫原性,尽管在血液恶性肿瘤中,这种方法的临床疗效数据有限。在淋巴瘤中使用独特型疫苗进行的 I/II 期试验取得令人鼓舞的结果后,三项 III 期试验的结果有些令人失望。目前正在开发其他一些有前途的策略来改善这些结果,包括优化抗原传递。在髓性白血病中,对来自多种白血病抗原(包括 WT1、PR1、RHAMM 和 BCR-ABL)的肽进行疫苗接种的临床试验显示出免疫原性的证据,但关于这种方法的临床疗效的数据有限。在这篇综述中,我们重点介绍了白血病和淋巴瘤疫苗接种临床试验的结果,并讨论了未来增强免疫疗法疗效的潜在策略。