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Contemporary Concise Review 2025: Interstitial Lung Disease
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Contemporary Concise Review 2025: Interstitial Lung Disease

Respirology·September 7Open Access
Respiratory SystemConfirms priorIdiopathic Pulmonary FibrosisInterstitial Lung AbnormalitiesInterstitial Lung DiseaseNarrative ReviewAntifibrotic TherapyAdult

Summary

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What was studied

A contemporary concise review (2025) summarizing recent advances in interstitial lung disease (ILD), covering updated nomenclature, early detection, interstitial lung abnormalities (ILAs), multi-omic biomarkers, quantitative imaging, and novel antifibrotic/targeted therapies.

Key findings

Key themes include: updated ILD classification aligning terminology with morphology and pathobiology; growing focus on early ILD detection and risk stratification in ILAs; emerging multi-omic biomarkers and quantitative imaging for prognostic stratification; and expanding antifibrotic/targeted therapies beyond IPF, with unmet needs in patient selection and treatment response.

Study limitations

As a narrative review, it does not provide primary data, pooled effect sizes, or systematic search methodology, limiting its evidentiary weight. Specific patient populations, sample sizes, and outcome data are not reported.

Clinical implications

Multidisciplinary discussion remains the foundation of ILD care; clinicians should be aware of updated ILD nomenclature and the expanding therapeutic landscape beyond IPF, including novel antifibrotics and targeted agents. Early identification of high-risk ILA patients and integration of molecular/imaging biomarkers may help guide individualized management.

Caveats

  • No specific drugs, brand names, or trial-level data are named in the abstract; tags reflect only what is directly stated.
  • Publication date (2026-09-07) is in the future relative to the review year cited (2025); this appears to be a 2025 literature review published in 2026, which is consistent with today's date.
  • This is a narrative review without systematic search criteria or meta-analytic methods; level of evidence is low (expert opinion/review).

Related Questions

Explore related topics

What are the latest antifibrotic therapies approved or in trials for non-IPF interstitial lung disease?How are multi-omic biomarkers being used to predict ILD progression in clinical practice?What criteria identify patients with interstitial lung abnormalities at high risk of progression to ILD?

Publication Details

Year
2026
Journal
Respirology
Source
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