Shabason Jacob E, Minn Andy J
Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Parker Institute for Cancer Immunotherapy, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Semin Radiat Oncol. 2017 Jul;27(3):289-298. doi: 10.1016/j.semradonc.2017.03.002. Epub 2017 Mar 16.
Immune escape of malignant cells is an important hallmark of cancer, necessary for tumor formation and progression. Accordingly, in recent years, therapies that enhance the immune system have had remarkable success in treating a myriad of malignancies. Particularly successful has been immune checkpoint blockade (ICB), which is a therapy that targets T-cell inhibitory receptors, or immune checkpoints. Despite these encouraging clinical results, most patients do not respond to such agents. Therefore, determining methods to better target and enhance the therapeutic efficacy of ICB is of paramount importance. One appealing approach is to use standard anticancer therapies, such as radiation, chemotherapy, and targeted biologics, to favorably modulate the immune system and enhance the anticancer immune response. For example, although radiation therapy has classically been thought of as a local therapy, there is significant potential for combining radiation therapy with ICB to both optimize local control and to treat metastatic disease. This concept is supported by numerous preclinical studies and clinical case reports and has since led to many early and ongoing clinical trials. However, it is still unclear how to optimally combine radiation and ICB to maximize the therapeutic effect. In this review, we highlight relevant preclinical and clinical studies in the field of radiation and ICB and discuss optimal strategies for combination therapies moving forward.
恶性细胞的免疫逃逸是癌症的一个重要标志,是肿瘤形成和进展所必需的。因此,近年来,增强免疫系统的疗法在治疗多种恶性肿瘤方面取得了显著成功。免疫检查点阻断(ICB)尤其成功,它是一种针对T细胞抑制受体或免疫检查点的疗法。尽管有这些令人鼓舞的临床结果,但大多数患者对此类药物没有反应。因此,确定更好地靶向和提高ICB治疗效果的方法至关重要。一种有吸引力的方法是使用标准的抗癌疗法,如放疗、化疗和靶向生物制剂,来有利地调节免疫系统并增强抗癌免疫反应。例如,尽管传统上放疗被认为是一种局部疗法,但将放疗与ICB联合使用在优化局部控制和治疗转移性疾病方面具有巨大潜力。这一概念得到了众多临床前研究和临床病例报告的支持,此后引发了许多早期和正在进行的临床试验。然而,目前仍不清楚如何最佳地联合放疗和ICB以最大化治疗效果。在这篇综述中,我们重点介绍了放疗和ICB领域的相关临床前和临床研究,并讨论了未来联合治疗的最佳策略。