Evidence map›Paper›PMID 40766328›Full record

ReviewFrontiers in immunology2025

Successful management of chronic eosinophilic pneumonia triggered by immune checkpoint inhibitor: a case report and literature review.

Yasuhito Suzuki, Junpei Saito, Satoshi Kubota, Masakazu Ikeda, Mami Rikimaru, Ryuki Yamada, Takahiro Kumanaka, Ryutaro Tanaka, Kentaro Kazama, Koshi Saito and 13 more

Abstract readCase ReportsReview
In one paragraph

Review in Frontiers in immunology, 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. Article
  2. Review
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

23 authors.

Yasuhito SuzukiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Junpei SaitoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Satoshi KubotaDepartment of Otolaryngology-Head and Neck Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Masakazu IkedaDepartment of Otolaryngology-Head and Neck Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Mami RikimaruDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Ryuki YamadaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takahiro KumanakaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Ryutaro TanakaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kentaro KazamaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Koshi SaitoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Rina HariganeDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Riko SatoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hikaru TomitaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Natsumi WatanabeDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takashi UmedaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Ryuichi TogawaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yuki SatoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takefumi NikaidoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Xintao WangDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenya KanazawaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yoshinori TaninoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Shigeyuki MuronoDepartment of Otolaryngology-Head and Neck Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yoko ShibataDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) enhance antitumor immunity by blocking inhibitory immune signals, but can lead to immune-related adverse events (irAEs). Therefore, effective management of irAEs is crucial during ICI therapy. We report the case of a 50-year-old man who was referred to our department due to cough and abnormal chest shadows. He was diagnosed with hypopharyngeal cancer, and underwent chemoradiotherapy, resulting in complete remission. However, metastatic tumors were detected, and partial lung resection was performed. After one-year, new metastatic tumors and pleural dissemination were identified. Therefore, treatment with pembrolizumab was initiated. After the treatment with pembrolizumab, chest imaging revealed ground-glass opacity (GGO). Laboratory tests showed elevated eosinophils, and fractional exhaled nitric oxide (FeNO). The findings of bronchoscopy revealed eosinophilic infiltration and intraluminal fibrosis, consistent with chronic eosinophilic pneumonia (EP). Based on these findings, he was diagnosed with pembrolizumab-induced chronic EP. Pembrolizumab was temporarily discontinued, and oral corticosteroids (OCS) were initiated. After the treatment of OCS, his symptoms and GGO were dramatically improved. Subsequently, pembrolizumab was resumed, and the hypopharyngeal cancer remains stable without recurrence of EP. This report presents the first pembrolizumab-induced chronic EP during treatment for hypopharyngeal cancer. The chronic EP was effectively managed with systemic corticosteroid therapy. Furthermore, pembrolizumab was resumed with close monitoring of blood eosinophil counts and FeNO levels, without worsening of EP. The results of the current case suggest that ICI-induced chronic EP is manageable, and in cases where ICI therapy exhibits significant efficacy against cancer, its treatment may be continued with careful monitoring of these parameters.

Indexed as

Antibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsPulmonary EosinophiliaAdrenal Cortex HormonesChronic DiseaseHumansMaleMiddle AgedTreatment OutcomeAdrenal Cortex HormonesAntibodies, Monoclonal, HumanizedImmune Checkpoint Inhibitorspembrolizumabblood eosinophilcorticosteroideosinophilic pneumoniafractional exhaled nitric oxideimmune checkpoint inhibitorsimmune-related adverse eventsinterstitial lung disease

Identifiers

PMID40766328
PMCPMC12321562

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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.