Mackall Crystal L, Merchant Melinda S, Fry Terry J
Paediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, 10 Center Drive, MSC 1104, Bethesda, MD 20892, USA.
Nat Rev Clin Oncol. 2014 Dec;11(12):693-703. doi: 10.1038/nrclinonc.2014.177. Epub 2014 Oct 28.
After decades of research, immunotherapies for cancer are demonstrating increasing success. These agents can amplify existent antitumour immunity or induce durable antitumour immune responses in a wide array of cancers. The spectrum of immunotherapeutics is broad, spanning monoclonal antibodies and their derivatives, tumour vaccines, and adoptive therapies using T cells and natural killer cells. Only a small number of immunotherapies have been tested in paediatric cancers, but impressive antitumour effects have already been observed. Mononclonal antibodies targeting GD2 that induce antibody-dependent cell-mediated cytotoxicity improve survival in high-risk neuroblastoma. Bi-specific monoclonal antibodies that simultaneously target CD19 and activate T cells can induce remission in acute B-cell lymphoblastic leukaemia (B-ALL) and adoptive immunotherapy using T cells genetically engineered to express chimeric antigen receptors targeting CD19 induce impressive responses in B-ALL. Efforts are underway to generate and test new immunotherapies in a wider array of paediatric cancers. Major challenges include a need to identify immunotherapy targets on the most lethal childhood cancers, to expand availability of technology-intense platforms, such as adoptive cell therapy, to optimize management of novel toxicities associated with this new class of cancer therapies and to determine how best to incorporate these therapies into standard treatment paradigms.
经过数十年的研究,癌症免疫疗法正显示出越来越高的成功率。这些药物可以增强现有的抗肿瘤免疫力,或在多种癌症中诱导持久的抗肿瘤免疫反应。免疫治疗药物的范围很广,包括单克隆抗体及其衍生物、肿瘤疫苗,以及使用T细胞和自然杀伤细胞的过继性疗法。仅有少数免疫疗法在儿童癌症中进行了测试,但已观察到令人印象深刻的抗肿瘤效果。靶向GD2并诱导抗体依赖性细胞介导的细胞毒性的单克隆抗体可提高高危神经母细胞瘤患者的生存率。同时靶向CD19并激活T细胞的双特异性单克隆抗体可诱导急性B淋巴细胞白血病(B-ALL)缓解,而使用经过基因工程改造以表达靶向CD19的嵌合抗原受体的T细胞进行过继性免疫治疗可在B-ALL中诱导出令人印象深刻的反应。目前正在努力研发并在更多类型的儿童癌症中测试新的免疫疗法。主要挑战包括需要确定最致命的儿童癌症的免疫治疗靶点,扩大技术密集型平台(如过继性细胞疗法)的可及性,优化与这类新型癌症疗法相关的新毒性的管理,以及确定如何最好地将这些疗法纳入标准治疗模式。