Evidence map›Paper›PMID 33936103›Full record

ArticleFrontiers in immunology2021

Novel Biomarkers of Dynamic Blood PD-L1 Expression for Immune Checkpoint Inhibitors in Advanced Non-Small-Cell Lung Cancer Patients.

Qiao Yang, Mingjing Chen, Jiaoyang Gu, Kai Niu, Xianlan Zhao, Linpeng Zheng, Zihan Xu, Yongxin Yu, Feng Li, Lingxin Meng and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 8 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 8 syntheses or guidelines pooled it.

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  2. Correlation between exosomal PD-L1 and prognosis in patients with cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Qiao YangCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Mingjing ChenCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Jiaoyang GuCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Kai NiuCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Xianlan ZhaoCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Linpeng ZhengCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Zihan XuCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Yongxin YuCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Feng LiCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Lingxin MengCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Zhengtang ChenCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Wenlei ZhuoCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Luping ZhangCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.
Jianguo SunCancer Institute, Xinqiao Hospital, Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) have become a high-profile regimen for malignancy recently. However, only a small subpopulation obtains long-term clinical benefit. How to select optimal patients by reasonable biomarkers remains a hot topic. Methods: Paired tissue samples and blood samples from 51 patients with advanced malignancies were collected for correlation analysis. Dynamic changes in blood PD-L1 (bPD-L1) expression, including PD-L1 mRNA, exosomal PD-L1 (exoPD-L1) protein and soluble PD-L1 (sPD-L1), were detected after 2 months of ICIs treatment in advanced non-small-cell lung cancer (NSCLC) patients. The best cutoff values for progression-free survival (PFS) and overall survival (OS) of all three biomarkers were calculated with R software. Results: In 51 cases of various malignancies, those with positive tissue PD-L1 (tPD-L1) had significantly higher PD-L1 mRNA than those with negative tPD-L1. In 40 advanced NSCLC patients, those with a fold change of PD-L1 mRNA ≥ 2.04 had better PFS, OS and best objective response (bOR) rate. In addition, a fold change of exoPD-L1 ≥ 1.86 was also found to be associated with better efficacy and OS in a cohort of 21 advanced NSCLC cases. The dynamic change of sPD-L1 was not associated with efficacy and OS. Furthermore, the combination of PD-L1 mRNA and exoPD-L1 could screen better patients for potential benefit from ICIs treatment. Conclusion: There was a positive correlation between bPD-L1 and tPD-L1 expression. Increased expression of PD-L1 mRNA, exoPD-L1, or both in early stage of ICIs treatment could serve as positive biomarkers of efficacy and OS in advanced NSCLC patients.

Indexed as

Antigens, NeoplasmB7-H1 AntigenBiomarkers, TumorCarcinoma, Non-Small-Cell LungFemaleHumansImmune Checkpoint InhibitorsLung NeoplasmsMaleMiddle AgedProgression-Free SurvivalTreatment OutcomeAntigens, NeoplasmB7-H1 AntigenBiomarkers, TumorImmune Checkpoint Inhibitorsbiomarkerblood PD-L1exosomeimmune checkpoint inhibitorsNSCLC

Identifiers

PMID33936103
PMCPMC8085403

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.