Evidence map›Paper›PMID 35718373›Full record

ArticleJournal for immunotherapy of cancer2022

Longitudinal plasma proteomic profiling of patients with non-small cell lung cancer undergoing immune checkpoint blockade.

Michal Harel, Coren Lahav, Eyal Jacob, Nili Dahan, Itamar Sela, Yehonatan Elon, Shani Raveh Shoval, Galit Yahalom, Iris Kamer, Alona Zer and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

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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

15 authors at 6 institutions in 2 countries.

Michal HarelOncoHost Ltd, Binyamina, Israel.
Coren LahavOncoHost Ltd, Binyamina, Israel.
Eyal JacobOncoHost Ltd, Binyamina, Israel.
Nili DahanOncoHost Ltd, Binyamina, Israel.
Itamar SelaOncoHost Ltd, Binyamina, Israel.
Yehonatan ElonOncoHost Ltd, Binyamina, Israel.
Shani Raveh ShovalOncoHost Ltd, Binyamina, Israel.
Galit YahalomOncoHost Ltd, Binyamina, Israel.
Iris KamerInstitute of Oncology, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Alona ZerOncology Center, Rambam Health Care Campus, Haifa, Israel.
Ofer SharonOncoHost Ltd, Binyamina, Israel.
David P CarboneJames Thoracic Oncology Center, Ohio State University Medical Center, Columbus, Ohio, USA.
Adam P DickerRadiation Oncology, Thomas Jefferson University Sidney Kimmel Medical College, Philadelphia, Pennsylvania, USA.
Jair BarInstitute of Oncology, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Yuval ShakedRappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel yshaked@technion.ac.il.ORCID 0000-0001-9037-3895
Rambam Health Care Campus · ILSheba Medical Center · ILTechnion – Israel Institute of Technology · ILTel Aviv University · ILThe Ohio State University Wexner Medical Center · USThomas Jefferson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have revolutionized the cancer therapy landscape due to long-term benefits in patients with advanced metastatic disease. However, robust predictive biomarkers for response are still lacking and treatment resistance is not fully understood.

methodsWe profiled approximately 800 pre-treatment and on-treatment plasma proteins from 143 ICI-treated patients with non-small cell lung cancer (NSCLC) using ELISA-based arrays. Different clinical parameters were collected from the patients including specific mutations, smoking habits, and body mass index, among others. Machine learning algorithms were used to identify a predictive signature for response. Bioinformatics tools were used for the identification of patient subtypes and analysis of differentially expressed proteins and pathways in each response group.

resultsWe identified a predictive signature for response to treatment comprizing two proteins (CXCL8 and CXCL10) and two clinical parameters (age and sex). Bioinformatic analysis of the proteomic profiles identified three distinct patient clusters that correlated with multiple parameters such as response, sex and TNM (tumors, nodes, and metastasis) staging. Patients who did not benefit from ICI therapy exhibited significantly higher plasma levels of several proteins on-treatment, and enrichment in neutrophil-related proteins.

conclusionsOur study reveals potential biomarkers in blood plasma for predicting response to ICI therapy in patients with NSCLC and sheds light on mechanisms underlying therapy resistance.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsBiomarkersHumansImmune Checkpoint InhibitorsPlasmaProteomicsAntineoplastic Agents, ImmunologicalBiomarkersImmune Checkpoint Inhibitorslung neoplasmstranslational medical researchtumor biomarkers

Identifiers

PMID35718373
PMCPMC9207924
OpenAlexW4283170479

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.