Evidence map›Paper›PMID 38534959›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

Outcomes of Patients with Non-Small Cell Lung Cancer and Brain Metastases Treated with the Upfront Single Agent Pembrolizumab: A Retrospective and Multicentric Study of the ESCKEYP GFPC Cohort.

Simon Nannini, Florian Guisier, Hubert Curcio, Charles Ricordel, Pierre Demontrond, Safa Abdallahoui, Seyyid Baloglu, Laurent Greillier, Christos Chouaid, Roland Schott

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
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 6 institutions in 1 country.

Simon NanniniDepartment of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.ORCID 0000-0003-3097-727X
Florian GuisierDepartment of Pneumology, UNIROUEN, LITIS Lab QuantIF Team EA4108, CHU Rouen, Normandie University, Rouen and Inserm CIC-CRB 1404, 76000 Rouen, France.ORCID 0000-0002-8166-7303
Hubert CurcioDepartment of Pneumology, Centre Régionale de Lutte Contre le Cancer François Baclesse, 14000 Caen, France.
Charles RicordelDepartment of Pneumology, Centre Hospitalier Universitaire, 35000 Rennes, France.
Pierre DemontrondDepartment of Pneumology, Centre Régionale de Lutte Contre le Cancer François Baclesse, 14000 Caen, France.ORCID 0000-0001-6399-3562
Safa AbdallahouiDepartment of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.
Seyyid BalogluDepartment of Radiological, Centre Hospitalier Universitaire de Strasbourg, 67200 Strasbourg, France.
Laurent GreillierMultidisciplinary Oncology and Therapeutic Innovations, APHM, INSERM, CNRS, CRCM, Hôpital Nord, Aix Marseille University, 13015 Marseille, France.
Christos ChouaidDepartment of Pneumology, Centre Hospitalier, 94000 Créteil, France.ORCID 0000-0002-4290-5524
Roland SchottDepartment of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.ORCID 0000-0002-7735-5366
Institut de Cancérologie Strasbourg · FRCentre François Baclesse · FRCentre Hospitalier Universitaire de Rennes · FRCentre National de la Recherche Scientifique · FRHôpitaux Universitaires de Strasbourg · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is the most common cause of brain metastasis (BM). Little is known about immune checkpoint inhibitor activity in the central nervous system, especially in patients receiving monotherapy for tumors with a tumor proportion score (TPS) ≥ 50%. This noninterventional, retrospective, multicenter study, conducted with the GFPC, included treatment-naïve patients strongly positive for PD-L1 (TPS ≥ 50%) with BM receiving first-line single-agent pembrolizumab treatment between May 2017 and November 2019. The primary endpoints were centrally reviewed intracranial overall response rates (ORRs), centrally reviewed intracranial progression-free survival (cPFS), extracranial PFS, and overall survival were secondary endpoints. Forty-three patients from five centers were included. Surgical or local radiation therapy was administered to 31 (72%) patients, mostly before initiating ICI therapy (25/31). Among 38/43 (88.4%) evaluable patients, the intracranial ORR was 73%. The median PFS was 8.3 months. The cerebral and extracerebral median PFS times were 9.2 and 5.3 months, respectively. The median OS was 25.5 months. According to multivariate analysis, BM surgery before ICI therapy was the only factor significantly associated with both improved PFS (HR = 0.44) and OS (HR = 0.45). This study revealed the feasibility and outcome of front-line pembrolizumab treatment in this population with BM.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBrain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsHumansRetrospective StudiesAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumabbrain metastasiscentral nervous systemimmunotherapynon-small cell lung cancerreal-life data

Identifiers

PMID38534959
PMCPMC10969391
OpenAlexW4393038879

What OpenQuestion holds

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LicenceCC BY
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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.