Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
Cancer Immunol Res. 2020 Feb;8(2):161-166. doi: 10.1158/2326-6066.CIR-19-0692.
Over the last decade, immunotherapy has rapidly changed the therapeutic landscape and prognosis for many hematologic malignancies and adult solid tumors. Despite this success, immunotherapy for pediatric solid tumors remains in the early stages of development, and significant clinical benefit has yet to be realized, with anti-GD2 for neuroblastoma being the exception. The limited neoepitope expression and paucity of T-cell infiltration into the immunosuppressive tumor microenvironment have hampered current established immunotherapies. Emerging approaches to recruit T cells, to convert phenotypically "cold" into "inflamed" tumors, and to vastly improve therapeutic indices hold exceptional promise. Here, we review these approaches, highlighting the role of the tumor microenvironment and novel antibody platforms to maximize the full clinical potential of immunotherapy in pediatric oncology.
在过去的十年中,免疫疗法迅速改变了许多血液系统恶性肿瘤和成人实体肿瘤的治疗前景和预后。尽管取得了这一成功,但儿科实体肿瘤的免疫疗法仍处于早期发展阶段,尚未实现显著的临床获益,神经母细胞瘤的抗 GD2 是一个例外。目前已有的免疫疗法受到限制,因为新抗原的表达有限,T 细胞浸润到免疫抑制性肿瘤微环境中也很稀少。新兴的方法包括招募 T 细胞、将表型上“冷”的肿瘤转化为“炎症”肿瘤,以及极大地提高治疗指数,这些方法都有着巨大的潜力。在这里,我们回顾了这些方法,强调了肿瘤微环境和新型抗体平台的作用,以最大限度地发挥免疫疗法在儿科肿瘤学中的全部临床潜力。