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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...

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Autores principales: Shi, Jiawei, Liu, Junwei, Tu, Xiaoxuan, Li, Bin, Tong, Zhou, Wang, Tian, Zheng, Yi, Shi, Hongyu, Zeng, Xun, Chen, Wei, Yin, Weiwei, Fang, Weijia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
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.
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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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