Gustafson Michael P, Bornschlegl Svetlana, Park Sean S, Gastineau Dennis A, Roberts Lewis R, Dietz Allan B, Hallemeier Christopher L
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
Adv Radiat Oncol. 2017 Aug 18;2(4):540-547. doi: 10.1016/j.adro.2017.08.003. eCollection 2017 Oct-Dec.
Stereotactic body radiation therapy (SBRT) can positively influence an antitumor immune response by inducing necrotic cell death. SBRT also been shown to eliminate tumors outside the radiation therapy field through an immune-mediated process known as the abscopal effect. Recent advances in immunotherapy may provide new therapeutic approaches for patients with liver cancer. Therefore, understanding the immune status of patients with cancer will likely guide how immunotherapy might be used in combination with SBRT. We hypothesized that we would observe changes in circulating blood immune cell populations of patients who received SBRT for liver tumors. Therefore, we assessed 110 immunophenotypes in the peripheral blood of 10 patients with liver cancer or metastases to the liver pretreatment and 2 posttreatment time points. Patients with liver cancer and metastatic patients both exhibited several immunophenotypic abnormalities at baseline compared with a group of healthy volunteer controls. In longitudinal studies, SBRT caused a specific reduction in CD3 T cell counts and immature CD56CD16 NK cell counts. The immune profiling and potential identification of circulating biomarkers shown here could lead to the design of combinatorial approaches with SBRT and immunotherapy to optimize the timing of treatment and direct the most effective immunotherapy with SBRT.
立体定向体部放射治疗(SBRT)可通过诱导坏死性细胞死亡对抗肿瘤免疫反应产生积极影响。SBRT还被证明可通过一种称为远隔效应的免疫介导过程消除放疗野之外的肿瘤。免疫治疗的最新进展可能为肝癌患者提供新的治疗方法。因此,了解癌症患者的免疫状态可能会指导免疫治疗如何与SBRT联合使用。我们假设,我们会观察到接受SBRT治疗肝肿瘤患者外周血免疫细胞群体的变化。因此,我们评估了10例肝癌或肝转移患者治疗前及治疗后2个时间点外周血中的110种免疫表型。与一组健康志愿者对照相比,肝癌患者和转移性患者在基线时均表现出几种免疫表型异常。在纵向研究中,SBRT导致CD3 T细胞计数和未成熟CD56CD16 NK细胞计数特异性降低。此处所示的循环生物标志物的免疫谱分析和潜在鉴定可能会促成SBRT与免疫治疗联合方法的设计,以优化治疗时机并指导最有效的SBRT免疫治疗。