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Classification of Non-Small Cell Lung Cancer's Tumor Immune Micro-Environment and Strategies to Augment Its Response to Immune Checkpoint Blockade.
Chi, Alexander; He, Xia; Hou, Lin; Nguyen, Nam P; Zhu, Guangying; Cameron, Robert B; Lee, Jay M.
Affiliation
  • Chi A; Department of Radiation Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101100, China.
  • He X; Department of Radiation Oncology, Jiangsu Cancer Hospital, Nanjing Medical University, Nanjing 210009, China.
  • Hou L; Department of Radiation Oncology, Jiangsu Cancer Hospital, Nanjing Medical University, Nanjing 210009, China.
  • Nguyen NP; Center for Statistical Science, Tsinghua University, Beijing 100084, China.
  • Zhu G; Department of Radiation Oncology, Howard University, Washington, DC 20060, USA.
  • Cameron RB; Department of Radiation Oncology, China-Japan Friendship Hospital, Beijing 100029, China.
  • Lee JM; Division of Thoracic Surgery, Department of Surgery, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Cancers (Basel) ; 13(12)2021 Jun 11.
Article in En | MEDLINE | ID: mdl-34208113
ABSTRACT
Immune checkpoint blockade (ICB) with checkpoint inhibitors has led to significant and durable response in a subset of patients with advanced stage EGFR and ALK wild-type non-small cell lung cancer (NSCLC). This has been consistently shown to be correlated with the unique characteristics of each patient's tumor immune micro-environment (TIME), including the composition and distribution of the tumor immune cell infiltrate; the expression of various checkpoints by tumor and immune cells, such as PD-L1; and the presence of various cytokines and chemokines. In this review, the classification of various types of TIME that are present in NSCLC and their correlation with response to ICB in NSCLC are discussed. This is conducted with a focus on the characteristics and identifiable biomarkers of different TIME subtypes that may also be used to predict NSCLC's clinical response to ICB. Finally, treatment strategies to augment response to ICB in NSCLC with unresponsive types of TIME are explored.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Cancers (Basel) Year: 2021 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Cancers (Basel) Year: 2021 Document type: Article Affiliation country: China