Literature DB >> 23265249

The evolving pharmacotherapy of pulmonary fibrosis.

Harpreet K Lota1, Athol U Wells.   

Abstract

INTRODUCTION: Novel compounds targeting various aspects of fibrogenesis have been developed consequent to the increasing knowledge of the pathogenetic mechanisms of the interstitial lung diseases (ILDs). The authors review the evolution of treatment approaches in the ILDs, informed by recent placebo-controlled trials, and discuss current clinical trials in which emerging pathogenetic mechanisms are targeted as novel therapeutic agents. AREAS COVERED: In idiopathic pulmonary fibrosis (IPF), recent randomised, placebo-controlled trials have tested the efficacy of new therapies, and although primary end points have not been met in most, treatment effects have been observed. The demonstration of harmful effects from widely used IPF therapies has been equally important. Pirfenidone and nintedanib are emerging agents that exert pleiotropic effects, reflective of the multiple mechanistic pathways of IPF. Treatment may necessitate a similarly multifaceted approach using combination regimens of antifibrotic and antioxidant agents in order to be effective. In other ILDs, including systemic sclerosis, other connective tissue diseases and pulmonary sarcoidosis, the inflammatory/fibrotic model remains appropriate. Studies in systemic sclerosis have provided 'proof of concept' data for immunosuppressive therapy in the prevention of disease progression but there is a continuing need for controlled clinical trials in the more prevalent ILDs. EXPERT OPINION: In IPF, significant treatment effects have been reported with pirfenidone, nintedanib and N-acetylcysteine. Combinations of these pleiotropic agents, along with future monotherapies, in 'oncological regimens' may hold the key to more effective IPF treatment. In disorders other than IPF, there is an ongoing need for the controlled evaluation of traditional anti-inflammatory and immunosuppressive therapies. 'Cohort enrichment' (the selective recruitment of patients most likely to progress) holds the key to the identification of worthwhile treatment benefits.

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Year:  2013        PMID: 23265249     DOI: 10.1517/14656566.2013.758250

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  9 in total

Review 1.  Cellular mechanisms of tissue fibrosis. 6. Purinergic signaling and response in fibroblasts and tissue fibrosis.

Authors:  David Lu; Paul A Insel
Journal:  Am J Physiol Cell Physiol       Date:  2013-12-18       Impact factor: 4.249

Review 2.  Anti-fibrotic nintedanib-a new opportunity for systemic sclerosis patients?

Authors:  Ana Catarina Duarte; Maria José Santos; Ana Cordeiro
Journal:  Clin Rheumatol       Date:  2017-10-16       Impact factor: 2.980

Review 3.  Epigenetic targets for novel therapies of lung diseases.

Authors:  Brian S Comer; Mariam Ba; Cherie A Singer; William T Gerthoffer
Journal:  Pharmacol Ther       Date:  2014-11-15       Impact factor: 12.310

Review 4.  Efficacy and safety of pirfenidone for idiopathic pulmonary fibrosis.

Authors:  Yoshito Takeda; Kazuyuki Tsujino; Takashi Kijima; Atsushi Kumanogoh
Journal:  Patient Prefer Adherence       Date:  2014-03-21       Impact factor: 2.711

Review 5.  Diagnosis and management of interstitial lung disease.

Authors:  Keith C Meyer
Journal:  Transl Respir Med       Date:  2014-02-13

6.  Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain--results of a Delphi Panel.

Authors:  Ferran Morell; Dirk Esser; Jonathan Lim; Susanne Stowasser; Alba Villacampa; Diana Nieves; Max Brosa
Journal:  BMC Pulm Med       Date:  2016-01-12       Impact factor: 3.317

7.  Statin Use Is Associated with Reduced Mortality in Patients with Interstitial Lung Disease.

Authors:  Signe Vedel-Krogh; Sune F Nielsen; Børge G Nordestgaard
Journal:  PLoS One       Date:  2015-10-16       Impact factor: 3.240

Review 8.  Efficacy of N-Acetylcysteine in Idiopathic Pulmonary Fibrosis: A Systematic Review and Meta-Analysis.

Authors:  Tong Sun; Jing Liu; De Wei Zhao
Journal:  Medicine (Baltimore)       Date:  2016-05       Impact factor: 1.889

9.  Antioxidants and NOX1/NOX4 inhibition blocks TGFβ1-induced CCN2 and α-SMA expression in dermal and gingival fibroblasts.

Authors:  Hannah Murphy-Marshman; Katherine Quensel; Xu Shi-Wen; Rebecca Barnfield; Jacalyn Kelly; Alex Peidl; Richard J Stratton; Andrew Leask
Journal:  PLoS One       Date:  2017-10-19       Impact factor: 3.240

  9 in total

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