Department of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
German Cancer Consortium (DKTK) Partnersite Tuebingen, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Front Immunol. 2019 Mar 12;10:407. doi: 10.3389/fimmu.2019.00407. eCollection 2019.
In order to compensate for the increased oxygen consumption in growing tumors, tumors need angiogenesis and vasculogenesis to increase the supply. Insufficiency in this process or in the microcirculation leads to hypoxic tumor areas with a significantly reduced pO2, which in turn leads to alterations in the biology of cancer cells as well as in the tumor microenvironment. Cancer cells develop more aggressive phenotypes, stem cell features and are more prone to metastasis formation and migration. In addition, intratumoral hypoxia confers therapy resistance, specifically radioresistance. Reactive oxygen species are crucial in fixing DNA breaks after ionizing radiation. Thus, hypoxic tumor cells show a two- to threefold increase in radioresistance. The microenvironment is enriched with chemokines (e.g., SDF-1) and growth factors (e.g., TGFβ) additionally reducing radiosensitivity. During recent years hypoxia has also been identified as a major factor for immune suppression in the tumor microenvironment. Hypoxic tumors show increased numbers of myeloid derived suppressor cells (MDSCs) as well as regulatory T cells (Ts) and decreased infiltration and activation of cytotoxic T cells. The combination of radiotherapy with immune checkpoint inhibition is on the rise in the treatment of metastatic cancer patients, but is also tested in multiple curative treatment settings. There is a strong rationale for synergistic effects, such as increased T cell infiltration in irradiated tumors and mitigation of radiation-induced immunosuppressive mechanisms such as PD-L1 upregulation by immune checkpoint inhibition. Given the worse prognosis of patients with hypoxic tumors due to local therapy resistance but also increased rate of distant metastases and the strong immune suppression induced by hypoxia, we hypothesize that the subgroup of patients with hypoxic tumors might be of special interest for combining immune checkpoint inhibition with radiotherapy.
为了补偿生长肿瘤中氧气消耗的增加,肿瘤需要血管生成和血管发生来增加供应。该过程或微循环的不足会导致缺氧肿瘤区域,pO2 显著降低,这反过来又会导致癌细胞生物学和肿瘤微环境发生改变。癌细胞表现出更具侵袭性的表型、干细胞特征,并且更容易形成转移和迁移。此外,肿瘤内缺氧赋予了治疗耐药性,特别是放射抵抗性。活性氧在电离辐射后固定 DNA 断裂中至关重要。因此,缺氧肿瘤细胞的放射抵抗性增加了两到三倍。微环境富含趋化因子(例如 SDF-1)和生长因子(例如 TGFβ),进一步降低了放射敏感性。近年来,缺氧也被确定为肿瘤微环境中免疫抑制的主要因素。缺氧肿瘤表现出更多的髓源抑制细胞(MDSC)以及调节性 T 细胞(Ts),并且细胞毒性 T 细胞的浸润和激活减少。放疗联合免疫检查点抑制在转移性癌症患者的治疗中呈上升趋势,并且也在多种治疗设置中进行了测试。协同作用具有很强的合理性,例如在辐照肿瘤中增加 T 细胞浸润,并减轻免疫检查点抑制引起的辐射诱导免疫抑制机制,例如 PD-L1 上调。鉴于缺氧肿瘤患者由于局部治疗耐药性导致的预后较差,但也由于缺氧诱导的远处转移率增加和强烈的免疫抑制,我们假设缺氧肿瘤患者亚组可能特别有兴趣将免疫检查点抑制与放疗结合使用。