Evidence mapPaperPMID 33178495Full record

ArticleOncoimmunology2020

Angiotensin-converting enzyme (ACE) inhibitor prescription affects non-small-cell lung cancer (NSCLC) patients response to PD-1/PD-L1 immune checkpoint blockers.

Soleine Medjebar, Caroline Truntzer, Anaïs Perrichet, Emeric Limagne, Jean-David Fumet, Corentin Richard, Arielle Elkrief, Bertrand Routy, Cédric Rébé, François Ghiringhelli

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
1.2field-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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 30 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

10 authors at 5 institutions in 3 countries.

Soleine MedjebarDepartment of Medical Oncology, GF Leclerc Centre, Dijon, France.
Caroline TruntzerPlatform of Transfer in Cancer Biology, GF Leclerc Centre, Dijon, France.
Anaïs PerrichetPlatform of Transfer in Cancer Biology, GF Leclerc Centre, Dijon, France.
Emeric LimagnePlatform of Transfer in Cancer Biology, GF Leclerc Centre, Dijon, France.
Jean-David FumetDepartment of Medical Oncology, GF Leclerc Centre, Dijon, France.
Corentin RichardPlatform of Transfer in Cancer Biology, GF Leclerc Centre, Dijon, France.
Arielle ElkriefResearch Centre for the University of Montréal (CRCHUM), Montréal. Hematology-Oncology Division, Department of Medicine, University of Montreal Healthcare Centre (CHUM), Montreal, Canada.
Bertrand RoutyResearch Centre for the University of Montréal (CRCHUM), Montréal. Hematology-Oncology Division, Department of Medicine, University of Montreal Healthcare Centre (CHUM), Montreal, Canada.
Cédric RébéPlatform of Transfer in Cancer Biology, GF Leclerc Centre, Dijon, France.
François GhiringhelliDepartment of Medical Oncology, GF Leclerc Centre, Dijon, France.
Université Bourgogne Franche-Comté · FRCentre Georges François Leclerc · FRCentre Hospitalier de l’Université de Montréal · CAInserm · FRNational Cancer Centre Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin-converting enzyme (ACE) inhibitors are frequently used to treat hypertension and congestive heart failure. Preclinical data show that ACE plays a role on both innate and adaptive immune responses. Since interactions between ACE inhibitors and immune checkpoint inhibitors (ICIs) have not been reported, the aim of this study is to investigate the influence of ACE inhibitors on non-small cell lung cancer (NSCLC) patients treated with programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) inhibitors. We conducted a retrospective cohort analysis of NSCLC patients treated with PD-1/PD-L1 inhibitors. Clinical and co-medication data as well as tumor biopsies were collected. Groups were defined according to patients' co-medications at the time of ICI initiation. Among the 178 patients included, 22 (13.1%) received ACE inhibitors. While baseline characteristics were similar in both groups, ACE inhibitors group had a shorter median PFS (Progression-Free Survival) compared to the control group: 1.97 vs. 2.56 months,

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsAngiotensin-Converting Enzyme InhibitorsAngiotensinsB7-H1 AntigenHumansImmune Checkpoint InhibitorsPrescriptionsProgrammed Cell Death 1 ReceptorProspective StudiesRetrospective StudiesAngiotensin-Converting Enzyme InhibitorsAngiotensinsAntineoplastic Agents, ImmunologicalB7-H1 AntigenImmune Checkpoint InhibitorsProgrammed Cell Death 1 Receptorangiotensin-converting enzymeimmune checkpointmacrophagesnon-small cell lung cancer

Identifiers

PMID33178495
PMCPMC7595630
OpenAlexW3096233695

What Socratic 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 Socratic graph.