Department of Surgery, School of Medicine, Trinity College Dublin, Dublin 8, Ireland.
Trinity St James' Cancer Institute, St James's Hospital Dublin, Dublin 8, Ireland.
Int J Mol Sci. 2021 Jan 22;22(3):1071. doi: 10.3390/ijms22031071.
Radiotherapy remains one of the contemporary cornerstones of cancer treatment in the neoadjuvant, curative, adjuvant and palliative settings, either in isolation or as a multimodal approach. Moreover, recent advances in targeted immune checkpoint therapy have firmly established immunotherapy as the fourth pillar in cancer therapy alongside surgery, chemotherapy and notably radiotherapy. There is emerging evidence to suggest both radioresistance and reduced efficacy of immune checkpoint blockade (ICB) are potentiated by the tumour microenvironment (TME) and in fact modulating aspects of this immunosuppressive milieu is instrumental to unlocking anti-tumour immunity. The response rates of Upper Gastrointestinal (UGI) malignancies to ICB remains modest at 10-15%, compared to melanoma at 20-40%. Harnessing the effects of radiotherapy through remodelling of the TME using ICB as a radiosensitisor is an avenue showing promise. Here we explore the rationale behind combining radiotherapy with ICB, as a symbiotic relationship in shifting the balance in favour of anti-tumour immunity. We discuss the effects of radiotherapy on immunogenic cell death, the concept of the abscopal effect, the importance of the cGAS STING pathway, and their relevance in the context of the tumour microenvironment. Furthermore, dosing and timing of radiotherapy and ICB is now being evaluated for its synergistic effects on host tumour immunity, and we review the ongoing efforts and current available literature for single agent and dual agent ICB in combination multimodal therapy for both locally advanced operable and metastatic disease of the upper gastrointestinal tract.
放疗仍然是新辅助、根治性、辅助和姑息治疗中癌症治疗的当代基石之一,无论是单独使用还是作为多模态方法。此外,靶向免疫检查点治疗的最新进展已将免疫疗法牢固确立为癌症治疗的第四大支柱,与手术、化疗和放疗并列。有新的证据表明,肿瘤微环境(TME)增强了放射抵抗和免疫检查点阻断(ICB)的疗效降低,事实上,调节这种免疫抑制环境的各个方面对于释放抗肿瘤免疫至关重要。与黑色素瘤 20-40%的反应率相比,上消化道(UGI)恶性肿瘤对 ICB 的反应率仅为 10-15%。通过将 ICB 作为放射增敏剂重塑 TME 以利用放疗的效果是一种有前途的方法。在这里,我们探讨了将放疗与 ICB 结合的基本原理,这是一种有利于抗肿瘤免疫的共生关系。我们讨论了放疗对免疫原性细胞死亡的影响、远隔效应的概念、cGAS STING 途径的重要性及其在肿瘤微环境中的相关性。此外,放疗和 ICB 的剂量和时间安排现在正在评估其对宿主肿瘤免疫的协同作用,我们还回顾了用于局部晚期可手术和转移性上消化道疾病的单药和双药 ICB 联合多模态治疗的正在进行的努力和当前可用文献。