Evidence map›Paper›PMID 39613338›Full record

ArticleJournal for immunotherapy of cancer2024

Antecedent viral immunization and efficacy of immune checkpoint blockade: an extensive serum antibody profile to predict outcomes in non-small cell lung cancer.

Filippo G Dall'Olio, Wael Salem Zrafi, Quentin Blampey, Francois-Xavier Danlos, Matthieu Roulleaux-Dugage, Gabriel Roman, Charles Naltet, Paul-Henry Cournède, Daniel Gautheret, Mihaela Aldea and 6 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Filippo G Dall'OlioDepartment of Head and Neck Oncology, Gustave Roussy, Villejuif, France.ORCID 0000-0003-0903-6109
Wael Salem ZrafiDepartment of Biostatistics and Bioinformatics, Gustave Roussy, Villejuif, France.
Quentin BlampeyCentraleSupelec, Gif-sur-Yvette, France.
Francois-Xavier DanlosDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.ORCID 0000-0003-1880-064X
Matthieu Roulleaux-DugageDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.
Gabriel RomanCDI Laboratories Inc, Baltimore, Maryland, USA.
Charles NaltetDepartment of Respiratory Diseases, Hôpital Paris Saint-Joseph, Paris, France.
Paul-Henry CournèdeUniversite Paris-Saclay, Gif-sur-Yvette, France.
Daniel GautheretUniversite Paris-Saclay, Gif-sur-Yvette, France.
Mihaela AldeaUniversite Paris-Saclay, Gif-sur-Yvette, France.
David PlanchardUniversite Paris-Saclay, Gif-sur-Yvette, France.
Fabrice BarlesiUniversite Paris-Saclay, Gif-sur-Yvette, France.
Aurelien MarabelleDrug Development Department (DITEP), Gustave Roussy, Villejuif, France.ORCID 0000-0002-5816-3019
Tyler HulettCDI Laboratories Inc, Baltimore, Maryland, USA.ORCID 0000-0003-4128-5834
Nathalie Chaput-GrasLaboratoire d'immunomonitoring En Oncologie, University Paris-Saclay, Faculty of Pharmacy, Gustave Roussy Cancer Campus, Villejuif, France.
Benjamin BesseUniversite Paris-Saclay, Gif-sur-Yvette, France benjamin.besse@gustaveroussy.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImmune checkpoint blockers (ICBs) revolutionized the treatment of patients with advanced non-small cell lung cancer (NSCLC) but only a fraction of them obtain a response, and clinical benefit from these treatments is often difficult to predict. The aim of our study is to unveil the potential implications of antibody response to previous viral infections in predicting response to ICBs in patients with NSCLC.

methodsSera from patients treated with ICBs alone, chemotherapy (CT) or a combination of CT-ICBs were analyzed with VirScan (CDI Labs, USA), a high-throughput method that comprehensively analyzes epitope-level antiviral IgG antibodies via programmable phage display and immunoprecipitation sequencing.Total number of unique positive peptides (tUP) was defined as the total number of non-overlapping positive "is a hit" peptides for each patient.

resultsOverall, 387 patients were included. Of them, 129 were treated with ICBs alone, 66 with CT-ICBs and 195 with CT alone. 90 out of 129 patients treated with ICBs alone received ICBs as a subsequent line of treatment, while CT-ICBs and CT were administered as upfront therapies.A higher tUP was correlated with improved overall survival in patients treated with ICBs, and confirmed in the multivariate model (HR 0.43, 95% CI 0.24, 0.79, p=0.006), while it was not in those treated with CT-ICBs (p=0.8) and CT alone (p=0.1).tUP was not correlated with programmed death-ligand 1 (PD-L1) expression, while at the transcriptome level it was correlated with several immune-related pathways, particularly involving B cells.

conclusionA higher number of viral peptides recognized by serum antibodies might reflect increased immune fitness, resulting in improved outcomes in ICBs treated patients with NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsAgedFemaleHumansMaleMiddle AgedTreatment OutcomeImmune Checkpoint InhibitorsAntibodyBiomarkerImmune Checkpoint InhibitorImmunizationLung Cancer

Identifiers

PMID39613338
PMCPMC11605809

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.