Evidence map›Paper›PMID 37536667›Full record

ArticleThoracic cancer2023

Investigation of response factors for monotherapy with immune checkpoint inhibitors in non-small cell lung cancer patients with PD-L1 expression <50.

Yutaka Takahara, Ryudai Abe, Nagae Sumito, Takuya Tanaka, Yoko Ishige, Ikuyo Shionoya, Kouichi Yamamura, Kazuaki Nishiki, Masafumi Nojiri, Ryo Kato and 2 more

Abstract read
In one paragraph

Article in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

12 authors.

Yutaka TakaharaDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.ORCID 0000-0001-6863-0074
Ryudai AbeDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Nagae SumitoDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Takuya TanakaDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Yoko IshigeDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Ikuyo ShionoyaDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Kouichi YamamuraDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Kazuaki NishikiDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Masafumi NojiriDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Ryo KatoDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Shohei ShinomiyaDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Taku OikawaDepartment of Respiratory Medicine, Kanazawa Medical University, Kahoku, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitor (ICI) monotherapy is currently approved for the treatment of advanced non-small cell lung cancer (NSCLC) patients with programmed death ligand-1 (PD-L1) expression ≥50%. However, the efficacy of ICI monotherapy in patients with PD-L1 expression <50% has not yet been fully elucidated. The aim of this study was to identify the clinical characteristics of NSCLC patients with PD-L1 expression <50% who respond to single-agent ICIs and factors that predict response.

methodsPatients with advanced or recurrent NSCLC with a PD-L1 tumor proportion score (TPS) of 50% or less who received new monotherapy with an ICI between July 2012 and December 2022 were retrospectively analyzed. Patients with response were compared with those without response in the post-treatment response assessment.

resultsAmong the 37 patients, six (16.2%) NSCLC patients in the response group responded to ICI monotherapy and had a significantly lower body mass index (BMI) (p = 0.003). Significantly more patients in the response group developed immune-related adverse events (irAEs) than in the nonresponse group (p < 0.001). Multivariate analysis identified high BMI as a significant independent risk factor predicting nonresponse to ICI monotherapy in NSCLC patients with PD-L1 < 50%.

conclusionsAmong NSCLC patients with PD-L1 < 50%, those with a higher BMI were more likely to be nonresponders to ICI monotherapy. In addition, the group that responded to ICI monotherapy may have been at higher risk of developing irAEs, suggesting that careful follow-up is warranted.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenHumansImmune Checkpoint InhibitorsRetrospective StudiesB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsBMIimmune checkpoint inhibitorirAENSCLCPD-L1

Identifiers

PMID37536667
PMCPMC10518233

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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.