Evidence map›Paper›PMID 40386739›Full record

ArticleTranslational lung cancer research2025

Impact of immune-related adverse events on clinical outcomes in patients with advanced non-small cell lung cancer with low PD-L1 expression, focusing on pneumonitis: a multicenter retrospective study in Japan.

Shiho Goda, Tadaaki Yamada, Kenji Morimoto, Tae Hata, Yasuhiro Goto, Akihiko Amano, Yoshiki Negi, Satoshi Watanabe, Naoki Furuya, Tomohiro Oba and 14 more

Abstract read
In one paragraph

Article in Translational lung cancer research, 2025. 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. Pulmonary toxicity of immune checkpoint inhibitors.Breathe (Sheffield, England) · 2026
    Review
  2. 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

24 authors.

Shiho GodaDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-8072-605X
Tadaaki YamadaDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-6945-281X
Kenji MorimotoDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0003-3394-1838
Tae HataDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-0598-2280
Yasuhiro GotoDepartment of Respiratory Medicine, Fujita Health University School of Medicine, Aichi, Japan.ORCID https://orcid.org/0000-0003-2235-8567
Akihiko AmanoDepartment of Respiratory Medicine, Kurashiki Central Hospital, Okayama, Japan.
Yoshiki NegiDepartment of Respiratory Medicine and Hematology, School of Medicine, Hyogo Medical University, Hyogo, Japan.ORCID https://orcid.org/0009-0006-5059-4654
Satoshi WatanabeDepartment of Respiratory Medicine and Infectious Disease, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.ORCID https://orcid.org/0000-0003-0041-6981
Naoki FuruyaDivision of Respiratory Medicine, Department of Internal Medicine, St Marianna University Hospital, Kanagawa, Japan.ORCID https://orcid.org/0000-0001-7162-5946
Tomohiro ObaDepartment of Respiratory Medicine, Saitama Red Cross Hospital, Saitama, Japan.
Tatsuki IkomaDepartment of Thoracic Oncology, Kansai Medical University Hospital, Osaka, Japan.ORCID https://orcid.org/0000-0003-3758-3425
Akira NakaoDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.ORCID https://orcid.org/0000-0001-8308-4227
Keiko TanimuraDepartment of Respiratory Medicine, Fukuchiyama City Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-7826-4466
Hirokazu TaniguchiClinical Oncology Center and Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.ORCID https://orcid.org/0000-0003-2414-8344
Akihiro YoshimuraDepartment of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-3753-2110
Tomoya FukuiDepartment of Respiratory Medicine, Shonan Kamakura General Hospital, Kanagawa, Japan.ORCID https://orcid.org/0000-0003-4814-4401
Daiki MurataDivision of Respirology, Neurology, and Rheumatology, Department of Internal Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-4295-5046
Kyoichi KairaDepartment of Respiratory Medicine, Saitama Medical University International Medical Center, Saitama, Japan.ORCID https://orcid.org/0000-0001-5548-7686
Shinsuke ShiotsuDepartment of Respiratory Medicine, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-7195-0770
Asuka OkadaDepartment of Respiratory Medicine, Saiseikai Suita Hospital, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0001-5854-2257
Makoto HibinoDepartment of Respiratory Medicine, Shonan Fujisawa Tokushukai Hospital, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-1638-5027
Yusuke ChiharaDepartment of Respiratory Medicine, Uji Tokushukai Medical Center, Kyoto, Japan.
Takashi KijimaDepartment of Respiratory Medicine and Hematology, School of Medicine, Hyogo Medical University, Hyogo, Japan.ORCID https://orcid.org/0000-0003-4249-4021
Koichi TakayamaDepartment of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-7723-8960

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Severe immune-related adverse events (irAEs) are often associated with combined immunotherapy and chemotherapy in patients with non-small cell lung cancer (NSCLC). However, their effect on clinical outcomes has yet to be fully elucidated. In this study, we investigated the impact of irAEs, particularly pneumonitis, on clinical outcomes in patients receiving combined immunotherapy and chemotherapy for NSCLC. Methods: We retrospectively enrolled 850 patients with programmed cell death ligand-1 (PD-L1) 1-49% advanced NSCLC who were treated with chemotherapy alone or with combined immunotherapy and chemotherapy as first-line treatment at 19 different institutions in Japan between March 2017 and June 2022. Using data from their medical records, we examined the type and severity of irAEs and their association with clinical outcomes, including overall survival (OS) and progression-free survival (PFS). Results: OS and PFS were not significantly different between patients with and without severe irAEs. However, in the group receiving combined immunotherapy and chemotherapy, those who developed pneumonitis within 42 days of treatment initiation had shorter OS and PFS, irrespective of the pneumonitis grade, and a worse prognosis than those who received chemotherapy alone. Additionally, early-onset pneumonitis was more likely in patients aged >75 years, those with high lactate dehydrogenase levels, and those receiving steroids or immunosuppressants, suggesting that these factors may contribute to the risk of early-onset pneumonitis. Conclusions: Early-onset pneumonitis is a poor prognostic factor in patients with PD-L1 1-49% advanced NSCLC receiving combined immunotherapy and chemotherapy. Further large-scale observational studies are warranted to confirm these findings. Keywords: Non-small cell lung cancer (NSCLC); severe immune-related adverse events (irAEs); pneumonitis.

Identifiers

PMID40386739
PMCPMC12082213

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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.