摘要
肿瘤免疫治疗是一种主要针对程序性死亡蛋白-1(PD-1)及其配体PD-L1的治疗方法。PD-1/PD-L1抑制剂在多种肿瘤中具有非常明显的临床获益和持久反应,但是整体反应率仍较低。研究发现PD-L1和肿瘤突变负荷可以预测免疫治疗效果,MSI-H/dMMR、TP53和KRAS等基因突变与免疫治疗疗效呈正相关;而MDM2/4、EGFR、ALK等基因则与免疫治疗效果呈负相关。
Tumor immunotherapy is a treatment method mainly for programmed cell death-1(PD-1)and its ligand PD-L1.PD-1/PD-L1 inhibitors have obvious clinical benefits and long-lasting responses in a variety of tumors.But overall response rates are still low.Studies show that PD-L1 and tumor mutation burden can predict the effect of immunotherapy.MSI-H/dMMR,TP53 and KRAS mutations are positively correlated with the effect of immunotherapy.While MDM2/4,EGFR,ALK and other genes are negatively correlated with the effect of immunotherapy.
作者
张敏
周丽娜
徐姗姗
陈骏
Zhang Min;Zhou Lina;Xu Shanshan;Chen Jun(Department of Oncology,Second Hospital of Dalian Medical University,Dalian 116000,China)
出处
《国际肿瘤学杂志》
CAS
2020年第8期487-491,共5页
Journal of International Oncology
基金
希思科-君实肿瘤免疫研究基金(Y-JS2019-034)。