Evidence map›Paper›PMID 41932994›Full record

ArticleScientific reports2026

Association of immune-related adverse events with survival in patients receiving immune checkpoint inhibitor plus chemotherapy for lung cancer.

Shinya Takada, Izumi Nasu, Ryuji Uozumi, Masahiro Kondo, Shuichi Nawata, Hirotoshi Iihara, Yohei Okumura, Hirokazu Hashishita, Masashi Takemoto, Takahiro Okada and 7 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

17 authors.

Shinya Takada *Department of Pharmacy, National Hospital Organization Hokkaido Cancer Center, Hokkaido, Japan.
Izumi Nasu *Division of Pharmaceutical Care Sciences, Keio University Graduate School of Pharmaceutical Sciences, Tokyo, Japan.
Ryuji UozumiDepartment of Industrial Engineering and Economics, Institute of Science Tokyo, Tokyo, Japan.
Masahiro KondoDepartment of Pharmacy, Nagoya City University East Medical Center, Nagoya, Japan.
Shuichi NawataDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
Hirotoshi IiharaDepartment of Pharmacy, Gifu University Hospital, Gifu, Japan.
Yohei OkumuraDepartment of Pharmacy, Keio University Hospital, Tokyo, Japan.
Hirokazu HashishitaDepartment of Pharmacy, National Hospital Organization Hokkaido Cancer Center, Hokkaido, Japan.
Masashi TakemotoDepartment of Pharmacy, Nagoya City University Midorimunicipal Hospital, Nagoya, Japan.
Takahiro OkadaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
Yu KitamuraDepartment of Cardiology and Respiratory Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Satoshi OizumiDepartment of Respiratory Medicine, National Hospital Organization Hokkaido Cancer Center, Hokkaido, Japan.
Satoshi FukudaDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Sojiro KusumotoRespiratory Medicine and Allergology, Showa University School of Medicine, Tokyo, Japan.
Junki EndoDepartment of Cardiology and Respiratory Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Hitoshi KawazoeDepartment of Pharmacy, Keio University Hospital, Tokyo, Japan. kawazoe-ht@keio.jp.ORCID http://orcid.org/0000-0002-0626-7908
Tomonori NakamuraDivision of Pharmaceutical Care Sciences, Keio University Graduate School of Pharmaceutical Sciences, Tokyo, Japan.

Funding

Japan Society for the Promotion of Science 20H04147Japan Society for the Promotion of Science 22K06776
6 · The paper itself

Abstract

The association of immune-related adverse events (irAEs) and baseline peripheral blood count ratios with the effectiveness of immune checkpoint inhibitor (ICI) plus chemotherapy in patients with non-small cell lung cancer (NSCLC) remains unclear. This multicenter, retrospective study analyzed data from 191 patients treated with pembrolizumab or atezolizumab plus chemotherapy as first-line therapy across five hospitals in Japan between December 2018 and March 2021. Progression-free survival (PFS) and overall survival (OS) were assessed in relation to irAEs within a 6-week landmark analysis and baseline peripheral blood count ratios using Cox proportional hazards models. IrAEs occurred in 70 patients (36.6%) and showed no substantial association with survival (PFS: hazard ratio [HR] = 1.04, 95% confidence interval [CI] = 0.70–1.53 and OS: HR = 0.82, 95% CI = 0.49–1.34). Conversely, baseline peripheral blood count ratios were considerably linked to survival. A higher neutrophil-to-lymphocyte ratio correlated with reduced PFS (adjusted HR = 1.62, 95% CI = 1.10–2.40) and OS (adjusted HR = 2.50, 95% CI = 1.53–4.09), with similar trends for the lymphocyte-to-monocyte and platelet-to-lymphocyte ratios. Collectively, these findings suggest that although irAEs were not predictive of survival, baseline blood count ratios can serve as prognostic biomarkers in patients with NSCLC receiving chemoimmunotherapy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsAgedAged, 80 and overAntibodies, Monoclonal, HumanizedFemaleHumansJapanMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesAntibodies, Monoclonal, HumanizedatezolizumabImmune Checkpoint InhibitorspembrolizumabAtezolizumabImmune checkpoint inhibitorsImmune-related adverse eventsNon-small cell lung cancerPembrolizumab

Identifiers

PMID41932994
PMCPMC13199438

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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.