Evidence map›Paper›PMID 40240963›Full record

ArticleBMC immunology2025

Incidence of severe adverse events in cancer patients after treatment with immune-checkpoint inhibitors during the COVID- 19 pandemic.

Sakiko Kimura, Hiroo Katsuya, Chiho Nakashima, Naoko Sueoka-Aragane, Koji Hayashida, Kazumi Sasaki, Rintaro Sogawa, Tatsuya Furuno, Moriyasu Yamauchi, Yoichiro Sugiyama and 11 more

Abstract read
In one paragraph

Article in BMC immunology, 2025. 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

21 authors.

Sakiko KimuraDepartment of Pharmacy, Saga University Hospital, 5-1-1 Nabeshima, Saga City, Saga, 849-8501, Japan. mochinag@cc.saga-u.ac.jp.
Hiroo KatsuyaDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Chiho NakashimaDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Naoko Sueoka-AraganeDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Koji HayashidaDepartment of Medical Information, Saga University Hospital, Saga City, Saga, Japan.
Kazumi SasakiCancer Center, Saga University Hospital, Saga City, Saga, Japan.
Rintaro SogawaDepartment of Pharmacy, Saga University Hospital, 5-1-1 Nabeshima, Saga City, Saga, 849-8501, Japan.
Tatsuya FurunoDepartment of Pharmacy, Saga University Hospital, 5-1-1 Nabeshima, Saga City, Saga, 849-8501, Japan.
Moriyasu YamauchiDepartment of Otolaryngology Head and Neck Surgery, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Yoichiro SugiyamaDepartment of Otolaryngology Head and Neck Surgery, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Hirokazu NoshiroDepartment of Surgery, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Motohiro EsakiDivision of Gastroenterology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Mitsuru NoguchiDepartment of Urology, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Hirokazu TakahashiLiver Center, Faculty of Medicine, Saga University Hospital, Saga University, Saga City, Saga, Japan.
Keizo AnzaiDivision of Metabolism and Endocrinology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Masatoshi YokoyamaDepartment of Obstetrics and Gynecology, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Kazunari SugitaDivision of Dermatology, Department Of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Yoshio YamashitaDepartment of Oral and Maxillofacial Surgery, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Atsushi KawaguchiEducation and Research Center for Community Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Shinya KimuraDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga City, Saga, Japan.
Chisato ShimanoeDepartment of Pharmacy, Saga University Hospital, 5-1-1 Nabeshima, Saga City, Saga, 849-8501, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune-checkpoint inhibitors (ICIs) can cause inflammation and immune-related adverse events (irAEs). Although irAEs may be caused by dysregulation of cytokines, the impact of various COVID- 19-related factors on expression of ICI-related AEs remains unclear. Assessment of AEs following ICI administration during the COVID- 19 pandemic may provide valuable insights that enable optimization of patient selection, thereby maximizing the benefits of ICI therapy. The aim of this study was to investigate the actual occurrence of severe AEs after ICI administration during the COVID- 19 pandemic. The medical records of patients who received ICI at Saga University Hospital were examined retrospectively. The primary endpoint was the incidence of all AEs ≥ Grade 3 that occurred after ICI administration. The survey period, from Jan 2020 to Dec 2022, was divided into an earlier (Jan 2020-March 2021) and a later (April 2021-Dec 2022) period. AEs with a clear cause other than ICI were excluded from the analysis. A total of 527 patients were included in the analysis, with a median follow-up of 422 days. During the COVID- 19 pandemic, the incidence of AEs ≥ Grade 3 after ICI administration was 52.8%. The incidence of AEs ≥ Grade 3 AEs after ICI administration was significantly higher during the later period [23.4% (57/244) in the earlier period and 49.8% (236/474) in the later period; mixed effect model p < 0.0001, odds ratio, 3.37 (95% CI: 2.32-4.89)]. Overall survival was significantly worse in the group with AEs ≥ Grade 3 than in the group without AEs ≥ Grade 3 [HR (95% CI) = 0.48 (0.36-0.65), p = 0.0001]. During the COVID- 19 pandemic, it became clear that the incidence of severe AEs (including irAEs) increased after ICI administration, particularly during the later period of the disease. Various factors may be associated with occurrence of severe AEs after ICI administration, and long-term careful observation and prospective multicenter clinical studies are required.

Indexed as

COVID-19Immune Checkpoint InhibitorsNeoplasmsSARS-CoV-2AdultAgedAged, 80 and overFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesImmune Checkpoint InhibitorsAdverse eventsCOVID- 19 pandemicImmune-checkpoint inhibitor

Identifiers

PMID40240963
PMCPMC12001417

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.