Evidence map›Paper›PMID 35729418›Full record

ArticleCancer immunology, immunotherapy : CII2023

First-line single-agent pembrolizumab for PD-L1-positive (tumor proportion score ≥ 50%) advanced non-small cell lung cancer in the real world: impact in brain metastasis: a national French multicentric cohort (ESCKEYP GFPC study).

Renaud Descourt, Laurent Greillier, Maurice Perol, Charles Ricordel, Jean-Bernard Auliac, Lionel Falchero, Radj Gervais, Rémi Veillon, Sabine Vieillot, Florian Guisier and 10 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 4 pooled it
2.6field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 4 syntheses or guidelines pooled it, 26 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

20 authors at 20 institutions in 1 country.

Renaud DescourtOncology Department, Brest University Hospital, Brest, France.
Laurent GreillierMultidisciplinary Oncology and Therapeutic Innovations Department, APHM, INSERM, CNRS, CRCM, Hôpital Nord, Aix Marseille University, Marseille, France.
Maurice PerolDepartment of Medical Oncology, Léon Bérard Cancer Center, Lyon, France.
Charles RicordelPneumology Department, Rennes University Hospital, Rennes, France.
Jean-Bernard AuliacPneumology Department, Creteil University Hospital, CHI Créteil, 40 Avenue de Verdun, 94010, Creteil, France.
Lionel FalcheroPneumology Department, Hôpital Nord-Ouest, Villefranche-sur-Saône Hospital, Gleize, France.
Radj GervaisOncology Department, Caen François-Baclesse Cancer Center, Caen, France.
Rémi VeillonPneumology Department, Bordeaux University Hospital, Bordeaux, France.
Sabine VieillotOncology Department, Perpignan Hospital, Perpignan, France.
Florian GuisierPneumology Department, Rouen University Hospital, Rouen, France.
Marie MarcqPneumology Department, La Roche-sur-Yon Hospital, La Roche-sur-Yon, France.
Grégoire JusteauOncology Department, Angers University Hospital, Angers, France.
Laurence Bigay-GamePneumology Department, Toulouse University Hospital, Toulouse, France.
Marie BernardiPneumology Department, Aix-en-Provence Hospital, Aix-en-Provence, France.
Pierre FournelOncology Department, Institut de Cancérologie de La Loire Lucien Neuwirth, Saint-Priest-en-Jarez, France.
Hélène DoubrePneumology Department, Hôpital Foch, Suresnes, France.
Julian PinsollePneumology Department, Chambéry Métropole Savoie Hospital, Chambéry, France.
Karim AmraneOncology Department, Morlaix Hospital, Morlaix, France.
Christos ChouaïdPneumology Department, Creteil University Hospital, CHI Créteil, 40 Avenue de Verdun, 94010, Creteil, France. Christos.chouaid@chicreteil.fr.ORCID http://orcid.org/0000-0002-4290-5524
Chantal DecroisettePneumology Department, Annecy Genevois Hospital, Annecy, France.
Assistance Publique – Hôpitaux de Paris · FRCentre François Baclesse · FRCentre Hospitalier Annecy Genevois · FRCentre Hospitalier de Perpignan · FRCentre Hospitalier de Vitré · FRCentre Hospitalier du Pays d'Aix · FRCentre Hospitalier Métropole Savoie · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Rouen · FRCentre National de la Recherche Scientifique · FRHôpital Foch · FRHôpital Pontchaillou · FRHospices Civils de Lyon · FRInserm · FRInstitute Cancer De La Loire Lucien Neuwirth · FRRoche (France) · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFew real-world data are available in patients with advanced metastatic non-small cell lung cancer (NSCLC) treated with first-line immunotherapy, particularly in those with brain metastases at treatment initiation.

methodsThis was a national, retrospective, multicenter study that consecutively included all patients with PD-L1-positive (tumor proportion score ≥ 50%) advanced NSCLC who initiated first-line treatment with pembrolizumab as a single agent between May 2017 (date of availability of pembrolizumab in this indication in France) to November 22, 2019 (approval of the pembrolizumab-chemotherapy combination). Data were collected from medical records with local response assessment.

resultsThe cohort included 845 patients and 176 (20.8%) had brain metastases at diagnosis. There were no significant differences in outcomes for patients with and without brain metastases: 9.2 (95% CI 5.6-15) and 8 (95% CI 6.7-9.2, p = 0.3) months for median progression-free survival (PFS) and, 29.5 (95% CI 17.2-NA) and 22 (95% CI 17.8-27.1, p = 0.3) months for median overall survival (OS), respectively. Overall response rates were 47% and 45% in patients with and without cerebral metastases. In multivariate analysis, performance status 2-4 vs. 0-1 and neutrophil-to-lymphocyte ratio ≥ 4 vs. < 4 were the main independent negative factors for OS; brain metastasis was not an independent factor for OS.

conclusionIn this large multicenter cohort, nearly 20% of patients initiating pembrolizumab therapy for advanced NSCLC had cerebral metastases. There was no significant difference in response rates, PFS and OS between patients with and without brain metastases.

Indexed as

Brain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenBrainHumansRetrospective StudiesAntibodies, Monoclonal, HumanizedB7-H1 AntigenpembrolizumabAdvanced stageBrain metastasesNon-small cell lung cancerPembrolizumabReal-world study

Identifiers

PMID35729418
PMCPMC10992810
OpenAlexW4283258954

What OpenQuestion holds

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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.