Evidence map›Paper›PMID 32099055›Full record

ArticleScientific reports2020

Clinical significance of circulating soluble immune checkpoint proteins in sorafenib-treated patients with advanced hepatocellular carcinoma.

Minh Phuong Dong, Masaru Enomoto, Le Thi Thanh Thuy, Hoang Hai, Vu Ngoc Hieu, Dinh Viet Hoang, Ayako Iida-Ueno, Naoshi Odagiri, Yuga Amano-Teranishi, Atsushi Hagihara and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.5field-weighted citation impact, top 3% of its field
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

37 citing papers in PubMed, 61 citations in OpenAlex.

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  13. Can Soluble Immune Checkpoint Molecules on Exosomes Mediate Inflammation?Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2022
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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 at 2 institutions in 1 country.

Minh Phuong DongDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Masaru EnomotoDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Le Thi Thanh ThuyDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Hoang HaiDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Vu Ngoc HieuDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Dinh Viet HoangDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Ayako Iida-UenoDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Naoshi OdagiriDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Yuga Amano-TeranishiDepartment of Hepatology, Osaka City General Hospital, Osaka, Japan.
Atsushi HagiharaDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Hideki FujiiDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Sawako Uchida-KobayashiDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Akihiro TamoriDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Norifumi KawadaDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan. kawadanori@med.osaka-cu.ac.jp.
Osaka City University · JPOsaka City General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In hepatocellular carcinoma (HCC), the clinical significance of soluble immune checkpoint protein levels as predictors of patient outcomes or therapeutic responses has yet to be defined. This study profiled the baseline levels of sixteen soluble checkpoint proteins and their changes following sorafenib treatment for HCC. Plasma samples were obtained from 53 patients with advanced HCC at baseline, week 1, 2 and 4 of sorafenib treatment and tested the concentrations of 16 soluble checkpoint proteins using multiplexed fluorescent bead-based immunoassays. Multivariate analysis showed high sBTLA levels at baseline were an independent predictor of poor overall survival (p = 0.038). BTLA was highly expressed in T cells and macrophages in peritumoral areas. At week 2, sCD27 levels were decreased compared to baseline. By contrast, the concentrations of most inhibitory proteins, including sBTLA, sLAG-3, sCTLA-4, sPD-1, sCD80, sCD86 and sPD-L1, had significantly increased. The fold-changes of soluble checkpoint receptors and their ligands, including sCTLA-4 with sCD80/sCD86, sPD-1 with sPD-L1; and the fold-changes of sCTLA-4 with sBTLA or sPD-1 were positively correlated. sBTLA may be a good biomarker for predicting overall survival in HCC patients. Sorafenib treatment in patients with advanced HCC revealed dynamic changes of soluble checkpoint protein levels.

Indexed as

AdultAgedAged, 80 and overB7-H1 AntigenBiomarkers, TumorCarcinoma, HepatocellularFemaleHumansLiver NeoplasmsMaleMiddle AgedProportional Hazards ModelsProtein Kinase InhibitorsReceptors, ImmunologicSorafenibSurvival RateB7-H1 AntigenBiomarkers, TumorBTLA protein, humanProtein Kinase InhibitorsReceptors, ImmunologicSorafenibTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID32099055
PMCPMC7042216
OpenAlexW3007848523

What OpenQuestion holds

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LicenceCC BY
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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.