Bhalla Neeraj, Brooker Rachel, Brada Michael
Clatterbridge Cancer Centre NHS Foundation Trust, Bebington, Wirral, Merseyside, UK.
Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
J Thorac Dis. 2018 May;10(Suppl 13):S1447-S1460. doi: 10.21037/jtd.2018.05.107.
Immunotherapy has become standard of care in advanced non-small cell lung cancer (NSCLC) in a number of settings. Radiotherapy remains an important and potentially curative treatment for localized and locally advanced NSCLC not amenable to surgery. While the principal cytotoxic effect of ionizing radiation is via DNA damage, the effect on tumour microenvironment, promoting dendritic cell presentation of tumour-derived antigens to T cells stimulating the host adaptive immune system to mount an immune response against tumours cells, has become of particular interest when combining immunomodulating agents with radiation. The 'abscopal effect' of radiation where non-irradiated metastatic lesions may respond to radiation may be immune-mediated, via radiation primed anti-tumour T cells. Immune priming by radiation offers the potential for increasing the efficacy of immunotherapy and this is subject to on-going clinical trials underpinned by immunological bioassays. Increasing understanding of the interaction between tumour, radiation and immune cells at a molecular level provides a further opportunity for intervention to enhance the potential synergy between radiation and immunotherapy. Applying the potential efficacy of combination therapy to clinical practice requires caution particularly to ensure the safety of the two treatment modalities in early phase clinical trials, many of which are currently underway. We review the biological basis for combining radiation and immunotherapy and examine the existing pre-clinical and clinical evidence and the challenges posed by the new combination of treatments.
免疫疗法在多种情况下已成为晚期非小细胞肺癌(NSCLC)的标准治疗方法。放疗对于无法进行手术的局限性和局部晚期NSCLC仍然是一种重要且可能治愈的治疗方法。虽然电离辐射的主要细胞毒性作用是通过DNA损伤,但当将免疫调节药物与放疗联合使用时,其对肿瘤微环境的影响,即促进树突状细胞将肿瘤衍生抗原呈递给T细胞,刺激宿主适应性免疫系统对肿瘤细胞产生免疫反应,已变得尤为重要。放疗的“远隔效应”,即未受照射的转移病灶可能对放疗产生反应,可能是通过放疗激活的抗肿瘤T细胞介导的免疫反应。放疗引发的免疫反应为提高免疫疗法的疗效提供了潜力,这一点正在由免疫生物测定支持的临床试验中进行研究。在分子水平上对肿瘤、放疗和免疫细胞之间相互作用的深入理解为干预提供了进一步的机会,以增强放疗和免疫疗法之间潜在的协同作用。将联合疗法的潜在疗效应用于临床实践需要谨慎,特别是要确保在早期临床试验中两种治疗方式的安全性,目前许多此类试验正在进行。我们回顾了放疗与免疫疗法联合应用的生物学基础,并研究了现有的临床前和临床证据以及这种新的联合治疗带来的挑战。