Evidence map›Paper›PMID 41234563›Full record

ArticleTranslational lung cancer research2025

Analysis of second-line therapy in patients with prior pneumonitis receiving first-line combination immunotherapy for advanced non-small cell lung cancer.

Noriyuki Ebi, Hiroyuki Inoue, Makoto Fujimoto, Ami Hirata, Maiya Chen, Natsumi Kushima, Yuuka Sakaki, Takato Ikeda, Yuki Shundo, Toyoshi Yanagihara and 1 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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Noriyuki EbiDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-3140-4748
Hiroyuki InoueDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-8071-8797
Makoto FujimotoDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Ami HirataDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Maiya ChenDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Natsumi KushimaDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Yuuka SakakiDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Takato IkedaDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Yuki ShundoDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Toyoshi YanagiharaDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Masaki FujitaDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Combination immunotherapy has become a standard first-line treatment for advanced non-small cell lung cancer (NSCLC). However, its application in patients with checkpoint inhibitor-related pneumonitis (CIP) remains challenging due to the risk of treatment-related pulmonary toxicity. While first-line outcomes in CIP patients are increasingly reported, data on the efficacy and safety of subsequent therapies are lacking. This study aimed to evaluate treatment patterns, survival outcomes, and the risk of pulmonary toxicity associated with second-line therapy in NSCLC patients with prior CIP after first-line immunotherapy. Methods: This retrospective study analyzed 159 patients with advanced or recurrent NSCLC treated with first-line combination immunotherapy at Fukuoka University Hospital between January 2019 and March 2024, including those who had previously received molecular targeted therapy for driver gene mutations. Patients were stratified based on baseline CIP status. Among them, 91 patients (19 prior CIP and 72 non-prior CIP) who received second-line therapy were evaluated for progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and drug-induced pneumonitis onset during second-line treatment. Results: Baseline CIP was present in 32 patients (20.1%). The transition rate to second-line therapy was 73% in the prior CIP group and 64% in the non-prior CIP group, with no statistically significant difference observed between the two groups (P=0.49), indicating that the presence of prior CIP did not clearly affect the likelihood of receiving secondary therapy. PFS following second-line treatment was similar between patients with and without prior CIP. However, OS tended to be shorter in the prior CIP group (6.4 Conclusions: Second-line cytotoxic chemotherapy following combination immunotherapy may be associated with shorter survival and increased pulmonary toxicity in NSCLC patients with prior CIP. Careful clinical decision-making, multidisciplinary consultation, and close monitoring are essential when initiating second-line treatment in this population.

Indexed as

Advanced non-small cell lung cancer (advanced NSCLC)checkpoint inhibitor-related pneumonitis (CIP)immune-related adverse events (irAEs)real-world clinical settingsecond-line therapy

Identifiers

PMID41234563
PMCPMC12605418

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.