Evidence map›Paper›PMID 34590015›Full record

ArticleJTO clinical and research reports2021

Salvage Immunotherapy With Pembrolizumab in Patients Hospitalized for Life-Threatening Complications of NSCLC.

Ferréol Roborel de Climens, Christos Chouaid, Claire Poulet, Vincent Leroy, Luc Stoven, Alexis Benjamin Cortot, Xavier Dhalluin, Clément Gauvain

Open access · goldAbstract read
In one paragraph

Article in JTO clinical and research reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

8 authors at 7 institutions in 1 country.

Ferréol Roborel de ClimensService de Pneumologie et Oncologie Thoracique, Centre Hospitalier Universitaire (CHU) Lille, Université de Lille, Lille, France.
Christos ChouaidService de Pneumologie, CHI Créteil, Institut national de la santé et de la recherche médicale (Inserm) U955, University Paris-Est Créteil (UPEC), The Mondor Institute for Biomedical Research (IMRB), équipe CEpiA, Créteil, France.
Claire PouletService de Pneumologie et Réanimation Respiratoire, CHU Amiens Picardie, Amiens, France.
Vincent LeroyService de Pneumologie et Oncologie Thoracique, Centre Hospitalier Universitaire (CHU) Lille, Université de Lille, Lille, France.
Luc StovenService de Pneumologie, CH Boulogne-sur-Mer, Boulogne-sur-Mer, France.
Alexis Benjamin CortotService de Pneumologie et Oncologie Thoracique, Centre Hospitalier Universitaire (CHU) Lille, Université de Lille, Lille, France.
Xavier DhalluinService de Pneumologie et Oncologie Thoracique, Centre Hospitalier Universitaire (CHU) Lille, Université de Lille, Lille, France.
Clément GauvainService de Pneumologie et Oncologie Thoracique, Centre Hospitalier Universitaire (CHU) Lille, Université de Lille, Lille, France.
Université de Lille · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Lille · FRCentre National de la Recherche Scientifique · FRHôpital Intercommunal de Créteil · FRUniversité d'été de Boulogne-sur-Mer · FRUniversité Polytechnique Hauts-de-France · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIt is not known whether patients with NSCLC who are hospitalized because of cancer-related complications are liable to benefit from salvage immunotherapy.

methodsThis is a multicenter observational study including five centers, which involve all patients with advanced-stage NSCLC exhibiting a level of programmed death-ligand 1 (PD-L1) greater than or equal to 1%, having been hospitalized because of complications attributed to the evolution of the NSCLC, and having started pembrolizumab treatment during their hospitalization because of a risk of clinical deterioration in the short term. The analysis measured overall survival (OS) and the rate of discharge to home at 3 months.

resultsThe study included 33 patients, including 28 (85%) with metastatic NSCLC and 27 (82%) under first-line treatment. The main causes of hospitalization were deterioration of the general condition (52%), acute respiratory failure (18%), and an uncontrolled infection owing to the tumor (15%). A total of 20 patients (60%) had a performance status greater than or equal to 2 and 15 (45%) were under oxygen therapy. A total of 29 patients (88%) had a PD-L1 greater than or equal to 50%. Five patients (15%) started pembrolizumab in the intensive care unit. The median OS was 4.3 months (95% confidence interval [CI]: 0.9-not reached), and the 6-month and 1-year OS rates were 41.5% (95% CI: 27.5%-62.6%) and 32.6% (95% CI: 19.0%-55.9%), respectively. The home discharge rate at 3 months was 39% (95% CI: 23%-58%).

conclusionsEven when initiated in patients hospitalized for a life-threatening clinical deterioration, pembrolizumab seems to prolong the survival of certain patients with high PD-L1 NSCLC. Prospective, controlled data are necessary to confirm these results.

Indexed as

Clinical alterationImmunotherapyInpatient settingLung cancer

Identifiers

PMID34590015
PMCPMC8474254
OpenAlexW3126003425

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.