Evidence map›Paper›PMID 31156344›Full record

ArticleJournal of medical biochemistry2019

Soluble sPD-L1 and Serum Amyloid A1 as Potential Biomarkers for Lung Cancer.

Dragana Jovanović, Marina Roksandić-Milenković, Jelena Kotur-Stevuljević, Vesna Ćeriman, Ivana Vukanić, Natalija Samardžić, Spasoje Popević, Branislav Ilić, Milija Gajić, Marioara Simon and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of medical biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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  16. IGFBP-4: A promising biomarker for lung cancer.Journal of medical biochemistry · 2021
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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

16 authors at 3 institutions in 2 countries.

Dragana JovanovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Marina Roksandić-MilenkovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Jelena Kotur-StevuljevićDepartment for Medical Biochemistry, Faculty of Pharmacy University of Belgrade, Belgrade, Serbia.
Vesna ĆerimanUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Ivana VukanićUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Natalija SamardžićUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Spasoje PopevićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Branislav IlićUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Milija GajićUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Marioara SimonPulmonology Clinic »Leon Danielo«, Cluj-Napoca, Romania.
Ioan SimonFaculty of Medicine »Iuliu Hatieganu«, University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Vesna Spasojević-KalimanovskaDepartment for Medical Biochemistry, Faculty of Pharmacy University of Belgrade, Belgrade, Serbia.
Milica BelićDepartment for Medical Biochemistry, Faculty of Pharmacy University of Belgrade, Belgrade, Serbia.
Damjan MirkovUniversity Hospital of Pulmonology, Clinical Center of Serbia, Belgrade, Serbia.
Zorica ŠumaracCenter for Medical Biochemistry, Clinical Center of Serbia, Belgrade, Serbia.
Vladislav MilenkovićClinic »Milenković«, Belgrade, Serbia.
University of Belgrade · RSCentar za Promociju Nauke · RSIuliu Hațieganu University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe objective of this prospective study was to evaluate whether soluble programmed cell death-1/programmed cell death-ligand 1 (PD-1/PD-L1) and serum amyloid A1 (SAA1) are potential diagnostic, predictive or prognostic biomarkers in lung cancer.

methodsLung cancer patients (n=115) with advanced metastatic disease, 101 with non-small cell lung cancer, NSCLC (77 EGFR wild-type NSCLC patients on chemotherapy, 15 EGFR mutation positive adenocarcinoma patients, 9 patients with mPD-L1 Expression ≥50% NSCLC - responders to immunotherapy), and 14 patients with small cell lung cancer (SCLC) were examined. ELISA method was used to determine sPD-L1 and SAA1 concentrations in patients' plasma.

resultsSignificantly higher blood concentrations of sPD-L1 and SAA1 were noted in lung cancer patients compared with a healthy control group. In PD-L1+ NSCLC patients, a significantly higher sPD-L1 level was noticed compared to any other lung cancer subgroup, as well as the highest average SAA1 value compared to other subgroups.

conclusionsIt seems that sPD-1/PD-L1 might be a potential biomarker, prognostic and/ or predictive, particularly in patients treated with immunotherapy. Serum amyloid A1 has potential to act as a good predictor of patients' survival, as well as a biomarker of a more advanced disease, with possibly good capability to predict the course of disease measured at different time points.

Indexed as

biomarkerPD-L1 positive NSCLCserum amyloid A1sPD-L1

Identifiers

PMID31156344
PMCPMC6534957
OpenAlexW2902565393

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.