Evidence map›Paper›PMID 41885927›Full record

ArticleCancer immunology, immunotherapy : CII2026

Clinical characteristics, prognostic factors, and feasibility of ICI continuation in immune checkpoint inhibitor-related pneumonitis.

Keisuke Masumoto, Kazuya Tsubouchi, Ryosuke Matsukane, Sai Yasukochi, Hiroaki Ogata, Tomotsugu Takano, Mayako Uchida, Isamu Okamoto

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 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

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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

8 authors.

Keisuke MasumotoDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Kazuya TsubouchiDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. tsubouchi.kazuya.442@m.kyushu-u.ac.jp.
Ryosuke MatsukaneDepartment of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.
Sai YasukochiDepartment of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.
Hiroaki OgataDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Tomotsugu TakanoDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Mayako UchidaDepartment of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.
Isamu OkamotoDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmune checkpoint inhibitor (ICI)-related pneumonitis (ICI-pneumonitis) is a serious complication, whose clinical course and optimal management strategies remain inadequately elucidated. This study clarified whether post-pneumonitis ICI continuation is safe and feasible, identified risk factors for fatal outcomes or successful continuation, and assessed whether findings from patients with lung cancer can be generalized to those with other malignancies.

methodsThis retrospective study analyzed data from 1,320 patients who received ICI therapy at Kyushu University Hospital between September 2014 and March 2023. Among these, 300 and 1,020 patients had lung and non-lung cancers, respectively. Clinical characteristics, treatment strategies, and outcomes were compared between the two groups. Predictors of fatal pneumonitis and successful ICI continuation were identified using univariable logistic regression.

resultsICI-pneumonitis occurred in 96 (7.3%) patients, with a higher incidence in those with lung cancer (14.0%, [42/300]) than in those with non-lung cancers (5.3%, [54/1020]). Clinical characteristics remained similar across cancer types post-pneumonitis. Diffuse alveolar damage pattern, grade ≥ 3 pneumonitis at diagnosis, and elevated C-reactive protein level were significant predictors of fatal pneumonitis. Among 34 patients who attempted ICI continuation, 20 (58.8%) maintained ICI treatment until disease progression. Successful ICI continuation showed a trend toward association with normal baseline lung parenchyma.

conclusionsThe similar characteristics of ICI-pneumonitis across malignancies support the generalizability of management strategies. Approximately one-fifth of patients successfully continued ICI therapy after pneumonitis. Systematic radiological surveillance and appropriate severity-based treatment may help optimize outcomes in patients receiving ICI therapy.

Indexed as

Immune Checkpoint InhibitorsLung NeoplasmsPneumoniaAgedAged, 80 and overFeasibility StudiesFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesImmune Checkpoint InhibitorsImmune checkpoint inhibitorImmune-related adverse eventLung cancerPneumonitis

Identifiers

PMID41885927
PMCPMC13022113

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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.