Evolving landscape of treatments targeting the microenvironment of liver metastases in non-small cell lung cancer

被引:0
|
作者
Zhu Lingling [1 ,2 ]
Yu Xianzhe [3 ]
Tang Xiaojun [1 ]
Hu Chenggong [4 ]
Wu Lei [5 ]
Liu Yanyang [6 ]
Zhou Qinghua [1 ]
机构
[1] Lung Cancer Center, Lung Cancer Institute, West China Hospital, Sichuan University, Chengdu, Sichuan, China
[2] Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, College of Polymer Science and Engineering, Sichuan University, Chengdu, Sichuan, China
[3] Department of Gastrointestinal Surgery, Chengdu Second People’s Hospital, Chengdu, Sichuan, China
[4] Department of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China
[5] Core Facility of West China Hospital, Sichuan University, Chengdu, Sichuan, China
[6] Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China
基金
中国国家自然科学基金;
关键词
Non-small cell lung cancer; Liver metastasis; Combination therapy; Immune checkpoint inhibitors; Immune tolerance; Immunotherapy;
D O I
暂无
中图分类号
R735.7 [肝肿瘤];
学科分类号
100214 ;
摘要
Liver metastases (LMs) are common in lung cancer. Despite substantial advances in diagnosis and treatment, the survival rate of patients with LM remains low as the immune-suppressive microenvironment of the liver allows tumor cells to evade the immune system. The impact of LMs on the outcomes of immune checkpoint inhibitors in patients with solid tumors has been the main focus of recent translational and clinical research. Growing evidence indicates that the hepatic microenvironment delivers paracrine and autocrine signals from non-parenchymal and parenchymal cells. Overall, these microenvironments create pre- and post-metastatic conditions for the progression of LMs. Herein, we reviewed the epidemiology, physiology, pathology and immunology, of LMs associated with non-small cell lung cancer and the role and potential targets of the liver microenvironment in LM in each phase of metastasis. Additionally, we reviewed the current treatment strategies and challenges that should be overcome in preclinical and clinical investigations. These approaches target liver elements as the basis for future clinical trials, including combinatorial interventions reported to resolve hepatic immune suppression, such as immunotherapy plus chemotherapy, immunotherapy plus radiotherapy, immunotherapy plus anti-angiogenesis therapy, and surgical resection.
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