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Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy
BACKGROUND: The early diagnosis of hepatocellular carcinoma (HCC) can greatly improve patients’ 5-year survival rate, and the early efficacy assessment is important for oncologists to harness the anti-programmed cell death protein 1 (PD-1) immunotherapy in patients with advanced HCC. The lack of eff...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804705/ https://www.ncbi.nlm.nih.gov/pubmed/35101942 http://dx.doi.org/10.1136/jitc-2021-003133 |
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author | Shi, Jiawei Liu, Junwei Tu, Xiaoxuan Li, Bin Tong, Zhou Wang, Tian Zheng, Yi Shi, Hongyu Zeng, Xun Chen, Wei Yin, Weiwei Fang, Weijia |
author_facet | Shi, Jiawei Liu, Junwei Tu, Xiaoxuan Li, Bin Tong, Zhou Wang, Tian Zheng, Yi Shi, Hongyu Zeng, Xun Chen, Wei Yin, Weiwei Fang, Weijia |
author_sort | Shi, Jiawei |
collection | PubMed |
description | BACKGROUND: The early diagnosis of hepatocellular carcinoma (HCC) can greatly improve patients’ 5-year survival rate, and the early efficacy assessment is important for oncologists to harness the anti-programmed cell death protein 1 (PD-1) immunotherapy in patients with advanced HCC. The lack of effective predicting biomarkers not only leads to delayed detection of the disease but also results in ineffective immunotherapy and limited clinical survival benefit. METHODS: We exploited the single-cell approach (cytometry by time of flight (CyTOF)) to analyze peripheral blood mononuclear cells from multicohorts of human samples. Immune signatures for different stages of patients with HCC were systematically profiled and statistically compared. Furthermore, the dynamic changes of peripheral immune compositions for both first-line and second-line patients with HCC after anti-PD-1 monotherapy were also evaluated and systematically compared. RESULTS: We identified stage-specific immune signatures for HCC and constructed a logistic AdaBoost-SVM classifier based on these signatures. The classifier provided superior performance in predicting early-stage HCC over the commonly used serum alpha-fetoprotein level. We also revealed the treatment stage-specific immune signatures from peripheral blood and their dynamical changing patterns, all of which were integrated to achieve early discrimination of patients with non-durable benefit for both first-line and second-line anti-PD-1 monotherapies. CONCLUSIONS: Our newly identified single-cell peripheral immune signatures provide promising non-invasive biomarkers for early detection of HCC and early assessment for anti-PD-1 immunotherapy efficacy in patients with advanced HCC. These new findings can potentially facilitate early diagnosis and novel immunotherapy for patients with HCC in future practice and further guide the utility of CyTOF in clinical translation of cancer research. TRIAL REGISTRATION NUMBERS: NCT02576509 and NCT02989922. |
format | Online Article Text |
id | pubmed-8804705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-88047052022-02-07 Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy Shi, Jiawei Liu, Junwei Tu, Xiaoxuan Li, Bin Tong, Zhou Wang, Tian Zheng, Yi Shi, Hongyu Zeng, Xun Chen, Wei Yin, Weiwei Fang, Weijia J Immunother Cancer Immunotherapy Biomarkers BACKGROUND: The early diagnosis of hepatocellular carcinoma (HCC) can greatly improve patients’ 5-year survival rate, and the early efficacy assessment is important for oncologists to harness the anti-programmed cell death protein 1 (PD-1) immunotherapy in patients with advanced HCC. The lack of effective predicting biomarkers not only leads to delayed detection of the disease but also results in ineffective immunotherapy and limited clinical survival benefit. METHODS: We exploited the single-cell approach (cytometry by time of flight (CyTOF)) to analyze peripheral blood mononuclear cells from multicohorts of human samples. Immune signatures for different stages of patients with HCC were systematically profiled and statistically compared. Furthermore, the dynamic changes of peripheral immune compositions for both first-line and second-line patients with HCC after anti-PD-1 monotherapy were also evaluated and systematically compared. RESULTS: We identified stage-specific immune signatures for HCC and constructed a logistic AdaBoost-SVM classifier based on these signatures. The classifier provided superior performance in predicting early-stage HCC over the commonly used serum alpha-fetoprotein level. We also revealed the treatment stage-specific immune signatures from peripheral blood and their dynamical changing patterns, all of which were integrated to achieve early discrimination of patients with non-durable benefit for both first-line and second-line anti-PD-1 monotherapies. CONCLUSIONS: Our newly identified single-cell peripheral immune signatures provide promising non-invasive biomarkers for early detection of HCC and early assessment for anti-PD-1 immunotherapy efficacy in patients with advanced HCC. These new findings can potentially facilitate early diagnosis and novel immunotherapy for patients with HCC in future practice and further guide the utility of CyTOF in clinical translation of cancer research. TRIAL REGISTRATION NUMBERS: NCT02576509 and NCT02989922. BMJ Publishing Group 2022-01-31 /pmc/articles/PMC8804705/ /pubmed/35101942 http://dx.doi.org/10.1136/jitc-2021-003133 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Immunotherapy Biomarkers Shi, Jiawei Liu, Junwei Tu, Xiaoxuan Li, Bin Tong, Zhou Wang, Tian Zheng, Yi Shi, Hongyu Zeng, Xun Chen, Wei Yin, Weiwei Fang, Weijia Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title | Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title_full | Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title_fullStr | Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title_full_unstemmed | Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title_short | Single-cell immune signature for detecting early-stage HCC and early assessing anti-PD-1 immunotherapy efficacy |
title_sort | single-cell immune signature for detecting early-stage hcc and early assessing anti-pd-1 immunotherapy efficacy |
topic | Immunotherapy Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804705/ https://www.ncbi.nlm.nih.gov/pubmed/35101942 http://dx.doi.org/10.1136/jitc-2021-003133 |
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