Department of Radiation Oncology, the First Hospital of China Medical University, Shenyang, China.
Department of Urology, the First Hospital of China Medical University, Shenyang, China.
J Cell Mol Med. 2020 Apr;24(8):4726-4735. doi: 10.1111/jcmm.15145. Epub 2020 Mar 11.
For a long time, the guidance for adjuvant chemoradiotherapy for lower grade glioma (LGG) lacks instructions on the application timing and order of radiotherapy (RT) and chemotherapy. We, therefore, aimed to develop indicators to distinguish between the different beneficiaries of RT and chemotherapy, which would provide more accurate guidance for combined chemoradiotherapy. By analysing 942 primary LGG samples from The Cancer Genome Atlas (TCGA) and the Chinese Glioma Genome Atlas (CGGA) databases, we trained and validated two gene signatures (Rscore and Cscore) that independently predicted the responsiveness to RT and chemotherapy (Rscore AUC = 0.84, Cscore AUC = 0.79) and performed better than a previous signature. When the two scores were combined, we divided patients into four groups with different prognosis after adjuvant chemoradiotherapy: RSCS (RT-sensitive and chemotherapy-sensitive), RSCR (RT-sensitive and chemotherapy-resistant), RRCS (RT-resistant and chemotherapy-sensitive) and RRCR (RT-resistant and chemotherapy-resistant). The order and dose of RT and chemotherapy can be adjusted more precisely based on this patient stratification. We further found that the RRCR group exhibited a microenvironment with significantly increased T cell inflammation. In silico analyses predicted that patients in the RRCR group would show a stronger response to checkpoint blockade immunotherapy than other patients.
长期以来,低级别胶质瘤 (LGG) 辅助放化疗的指导意见缺乏关于放疗 (RT) 和化疗应用时机和顺序的说明。因此,我们旨在开发区分不同 RT 和化疗受益人群的指标,为联合放化疗提供更准确的指导。通过分析来自癌症基因组图谱 (TCGA) 和中国胶质瘤基因组图谱 (CGGA) 数据库的 942 个原发性 LGG 样本,我们训练和验证了两个独立预测 RT 和化疗反应性的基因特征 (Rscore 和 Cscore) (Rscore AUC=0.84,Cscore AUC=0.79),并且表现优于以前的特征。当这两个评分结合时,我们将患者分为辅助放化疗后预后不同的四组:RSCS(RT 敏感和化疗敏感)、RSCR(RT 敏感和化疗耐药)、RRCS(RT 耐药和化疗敏感)和 RRCR(RT 耐药和化疗耐药)。可以根据这种患者分层更精确地调整 RT 和化疗的顺序和剂量。我们进一步发现,RRCR 组表现出 T 细胞炎症明显增加的微环境。计算分析预测,RRCR 组患者对检查点阻断免疫疗法的反应会比其他患者更强。