2022
DOI: 10.3389/fonc.2021.716042
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Deciphering the Immune–Tumor Interplay During Early-Stage Lung Cancer Development via Single-Cell Technology

Abstract: Lung cancer is the leading cause of cancer-related death worldwide. Cancer immunotherapy has shown great success in treating advanced-stage lung cancer but has yet been used to treat early-stage lung cancer, mostly due to lack of understanding of the tumor immune microenvironment in early-stage lung cancer. The immune system could both constrain and promote tumorigenesis in a process termed immune editing that can be divided into three phases, namely, elimination, equilibrium, and escape. Current understanding… Show more

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Cited by 5 publications
(5 citation statements)
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References 136 publications
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“…The PhenoTIL model for adenocarcinomas (M AD ) and squamous cell carcinoma (M SCC ) were trained with most patients with early-stage (I and II) lung cancer, and the validation cohorts corresponded to patients from a plurality of staging groups (58.45%), indicating that the signatures were not specific to a particular disease stage, but the prognostic trend was observed most emphatically for early-stage disease. Most likely the immune reaction across the stages is highly variable, with latestage immune landscape predominantly characterized by high levels of T-cell exhaustion 41 and early-stage represented by a gradual transition from immune activation to immunosuppression, including the decrease of T-cell clonotypes, increase in regulatory T-cells infiltration and reduced infiltration of anti-tumor helper T cells 42 . For instance, despite PhenoTIL model M AD not having a statistically significant stratification of risk (p = 0.12, HR = 1.27 (0.93-1.7)) in the phase 3 clinical trial cohort D 8 (NCT01673867) of patients who received just Nivolumab, the Kaplan-Meir plots clearly revealed distinct risk groups (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The PhenoTIL model for adenocarcinomas (M AD ) and squamous cell carcinoma (M SCC ) were trained with most patients with early-stage (I and II) lung cancer, and the validation cohorts corresponded to patients from a plurality of staging groups (58.45%), indicating that the signatures were not specific to a particular disease stage, but the prognostic trend was observed most emphatically for early-stage disease. Most likely the immune reaction across the stages is highly variable, with latestage immune landscape predominantly characterized by high levels of T-cell exhaustion 41 and early-stage represented by a gradual transition from immune activation to immunosuppression, including the decrease of T-cell clonotypes, increase in regulatory T-cells infiltration and reduced infiltration of anti-tumor helper T cells 42 . For instance, despite PhenoTIL model M AD not having a statistically significant stratification of risk (p = 0.12, HR = 1.27 (0.93-1.7)) in the phase 3 clinical trial cohort D 8 (NCT01673867) of patients who received just Nivolumab, the Kaplan-Meir plots clearly revealed distinct risk groups (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Lung cancer is a multifaceted disease characterized by intricate regulatory mechanisms involving malignant cells, immune cells, stromal cells and aberrant signaling pathways within a complex ecosystem 49,50 . Therefore, it is challenging to accurately describe the molecular environment of the disease using a single marker.…”
Section: Discussionmentioning
confidence: 99%
“…Cancer immunoediting is the process of interaction and mutual influence between tumor cells and the body's immune system (20,21). Cancer immune regulation consists of three stages, namely, 1) elimination phase, 2) equilibrium phase and 3) escape phase (22,23). During the elimination phase, the mutated "non-self" cells in the body are recognized and eliminated specifically by the surveillance function of the immune system (24).…”
Section: Immune Regulation In Tumorsmentioning
confidence: 99%