Evidence map›Paper›PMID 41455752›Full record

ArticleScientific reports2025

Prognostic factors in patients with interstitial lung disease treated with nintedanib: a multicenter retrospective study in Japan.

Shiho Goda, Tadaaki Yamada, Yasuhiro Goto, Sayaka Uda, Akira Nakao, Shinsuke Shiotsu, Yuji Kukida, Keiko Tanimura, Akifumi Miyamoto, Yuki Imasato and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 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. 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

23 authors.

Shiho GodaDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Tadaaki YamadaDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan. tayamada@koto.kpu-m.ac.jp.
Yasuhiro GotoDepartment of Respiratory Medicine, Fujita Health University School of Medicine, Toyoake, 470-1192, Japan.
Sayaka UdaDepartment of Respiratory Medicine, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, 605-0981, Japan.
Akira NakaoDepartment of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, 814-0133, Japan.
Shinsuke ShiotsuDepartment of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, 602-8026, Japan.
Yuji KukidaDepartment of Rheumatology, Japanese Red Cross Kyoto Daini Hospital, Kyoto, 602-8026, Japan.
Keiko TanimuraDepartment of Respiratory Medicine, Fukuchiyama City Hospital, Fukuchiyama, 620-8505, Japan.
Akifumi MiyamotoDepartment of Respiratory Medicine, Rakuwakai Otowa Hospital, Kyoto, 607-8062, Japan.
Yuki ImasatoDepartment of Respiratory Medicine, Omi Medical Center, Kusatsu, 525-8585, Japan.
Asuka OkadaDepartment of Respiratory Medicine, Saiseikai Suita Hospital, Suita, 564-0013, Japan.
Isao HasegawaDepartment of Respiratory Medicine, Saiseikai Shigaken Hospital, Ritto, 520-3046, Japan.
Koji DateDepartment of Pulmonary Medicine, Kyoto Chubu Medical Center, Nantan, 629-0197, Japan.
Yohei MatsuiDepartment of Respirology, North Medical Center, Kyoto Prefectural University of Medicine, Yosa, 629-2261, Japan.
Shoki MoritoDepartment of Respiratory Medicine, Uji Tokushukai Medical Center, Uji, 611-0041, Japan.
Noeru InoguchiDepartment of Respiratory Medicine, Otsu City Hospital, Otsu, 520-0804, Japan.
Shuji OsugiDepartment of Respiratory Medicine, Japan Community Health Care Organization Kobe Central Hospital, Kobe, 651-1145, Japan.
Hayato KawachiDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Naoya NishiokaDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Masahiro IwasakuDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Shinsaku TokudaDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.
Tomohiro HandaDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, 606-8507, Japan.
Koichi TakayamaDepartment of Pulmonary Medicine, Graduate School of Medical science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nintedanib is widely used to slow disease progression and prevent acute exacerbations in patients with idiopathic pulmonary fibrosis (IPF) and progressive fibrosing interstitial lung disease (PF-ILD). We retrospectively analysed patients who initiated nintedanib for IPF or PF-ILD between August 2019 and July 2023 across 15 institutions in Japan, focusing on prognosis and disease progression. Patients were divided into two groups based on whether they survived for ≥ 3 years after nintedanib initiation, and their characteristics were compared. We also evaluated factors associated with annual forced vital capacity (FVC) decline and acute exacerbations. A total of 413 patients (171 with IPF and 242 with PF-ILD) were included. Median survival was 1,177 days for IPF and 1,268 days for PF-ILD, with no significant difference (P = 0.20). Patients surviving < 3 years were older (75.0 vs. 71.0 years), more frequently had resting arterial oxygen saturation (SpO2) < 95% (44.5% vs. 18.0%), and lower body mass index (BMI) (21.9 vs. 24.1 kg/m2). Additionally, patients with a BMI < 22 kg/m2 showed greater annual relative FVC decline. In conclusion, patients with IPF and PF-ILD showed comparable outcomes following nintedanib treatment. Age ≥ 65 years, resting SpO2 < 95%, and BMI < 22 kg/m2 were associated with shorter survival after nintedanib initiation.

Indexed as

Idiopathic Pulmonary FibrosisIndolesLung Diseases, InterstitialAgedAged, 80 and overDisease ProgressionFemaleHumansJapanMaleMiddle AgedPrognosisProtein Kinase InhibitorsRetrospective StudiesVital CapacityIndolesnintedanibProtein Kinase InhibitorsFibrosisInterstitial lung diseaseNintedanibPrognostic factorSurvivalTreatment

Identifiers

PMID41455752
PMCPMC12855916

What Socratic holds

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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 Socratic graph.