Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review

Abstract The spectrum of interstitial lung diseases (ILDs) includes a wide range of clinical entities with variable disease courses and prognoses. Several ILDs other than idiopathic pulmonary fibrosis (IPF) may exhibit a progressive fibrotic phenotype, with diverse clinical presentation, histopathol...

Full description

Saved in:
Bibliographic Details
Main Authors: Ignacio Español Montero, Fernanda Hernandez-Gonzalez, Jacobo Sellares
Format: Article
Language:English
Published: Adis, Springer Healthcare 2025-06-01
Series:Pulmonary Therapy
Subjects:
Online Access:https://doi.org/10.1007/s41030-025-00302-5
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849226099201933312
author Ignacio Español Montero
Fernanda Hernandez-Gonzalez
Jacobo Sellares
author_facet Ignacio Español Montero
Fernanda Hernandez-Gonzalez
Jacobo Sellares
author_sort Ignacio Español Montero
collection DOAJ
description Abstract The spectrum of interstitial lung diseases (ILDs) includes a wide range of clinical entities with variable disease courses and prognoses. Several ILDs other than idiopathic pulmonary fibrosis (IPF) may exhibit a progressive fibrotic phenotype, with diverse clinical presentation, histopathological and radiological patterns, as well as varying rates of disease progression and uncertain epidemiology, but with a similar prognosis of untreated idiopathic pulmonary fibrosis with irreversible lung function deterioration, substantial worsening of quality of life and early mortality. The recently defined term “progressive pulmonary fibrosis” (PPF) stands as an opportunity to better classify patients with progressive fibrotic disease and other IPF, irrespective of the underlying ILD. The definition of disease progression, including factors such as pulmonary function test decline, radiological progression, and symptomatic worsening, was not adopted until recently, thus significantly impacting the certainty of current estimates of incidence and prevalence and prognostic outcomes. Understanding disease progression in the broad spectrum of potentially progressive ILDs is key for developing standardized management algorithms irrespective of the ILD diagnosis. Current evidence points towards the potential beneficial effect of antifibrotic drugs in lung function decline and overall outcomes in several non-IPF progressive ILDs showing progression despite optimal management.
format Article
id doaj-art-df5d80fade9f414a9fa6424f47ef7a55
institution Kabale University
issn 2364-1754
2364-1746
language English
publishDate 2025-06-01
publisher Adis, Springer Healthcare
record_format Article
series Pulmonary Therapy
spelling doaj-art-df5d80fade9f414a9fa6424f47ef7a552025-08-24T11:42:35ZengAdis, Springer HealthcarePulmonary Therapy2364-17542364-17462025-06-0111334736310.1007/s41030-025-00302-5Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature ReviewIgnacio Español Montero0Fernanda Hernandez-Gonzalez1Jacobo Sellares2Pneumology and Respiratory Allergy Department, Hospital Clinic de Barcelona-IDIBAPSPneumology and Respiratory Allergy Department, Hospital Clinic de Barcelona-IDIBAPSPneumology and Respiratory Allergy Department, Hospital Clinic de Barcelona-IDIBAPSAbstract The spectrum of interstitial lung diseases (ILDs) includes a wide range of clinical entities with variable disease courses and prognoses. Several ILDs other than idiopathic pulmonary fibrosis (IPF) may exhibit a progressive fibrotic phenotype, with diverse clinical presentation, histopathological and radiological patterns, as well as varying rates of disease progression and uncertain epidemiology, but with a similar prognosis of untreated idiopathic pulmonary fibrosis with irreversible lung function deterioration, substantial worsening of quality of life and early mortality. The recently defined term “progressive pulmonary fibrosis” (PPF) stands as an opportunity to better classify patients with progressive fibrotic disease and other IPF, irrespective of the underlying ILD. The definition of disease progression, including factors such as pulmonary function test decline, radiological progression, and symptomatic worsening, was not adopted until recently, thus significantly impacting the certainty of current estimates of incidence and prevalence and prognostic outcomes. Understanding disease progression in the broad spectrum of potentially progressive ILDs is key for developing standardized management algorithms irrespective of the ILD diagnosis. Current evidence points towards the potential beneficial effect of antifibrotic drugs in lung function decline and overall outcomes in several non-IPF progressive ILDs showing progression despite optimal management.https://doi.org/10.1007/s41030-025-00302-5Progressive pulmonary fibrosisInterstitial lung diseasesAntifibrotic therapyDisease progression
spellingShingle Ignacio Español Montero
Fernanda Hernandez-Gonzalez
Jacobo Sellares
Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
Pulmonary Therapy
Progressive pulmonary fibrosis
Interstitial lung diseases
Antifibrotic therapy
Disease progression
title Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
title_full Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
title_fullStr Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
title_full_unstemmed Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
title_short Epidemiology and Prognosis of Progressive Pulmonary Fibrosis: A Literature Review
title_sort epidemiology and prognosis of progressive pulmonary fibrosis a literature review
topic Progressive pulmonary fibrosis
Interstitial lung diseases
Antifibrotic therapy
Disease progression
url https://doi.org/10.1007/s41030-025-00302-5
work_keys_str_mv AT ignacioespanolmontero epidemiologyandprognosisofprogressivepulmonaryfibrosisaliteraturereview
AT fernandahernandezgonzalez epidemiologyandprognosisofprogressivepulmonaryfibrosisaliteraturereview
AT jacobosellares epidemiologyandprognosisofprogressivepulmonaryfibrosisaliteraturereview