Literature DB >> 16315778

A critical assessment of treatment options for idiopathic pulmonary fibrosis.

Nirav R Shah1, Paul Noble, Robert M Jackson, Talmadge E King, Steven D Nathan, Maria Padilla, Ganesh Raghu, Melissa Bruce Rhodes, Marvin Schwarz, Gregory Tino, Robert W Dubois.   

Abstract

BACKGROUND: To date, no management approach has proven to be efficacious for the treatment of idiopathic pulmonary fibrosis (IPF). Consequently, therapeutic options remain controversial and confusing for many clinicians. We sought to formally review available evidence on treatment options for IPF and to have a diverse panel of physicians rate the "appropriateness," "inappropriateness," or "uncertainty" of some of the available therapeutic options.
METHODS: The RAND/UCLA Appropriateness Method was used to review and rate multiple clinical scenarios for the treatment of IPF. The panel was composed of nine physicians from geographically diverse areas who received a systematic review on the risks and benefits of commonly used treatments for IPF as background.
RESULTS: A total of 324 clinical scenarios were rated: 25% as appropriate; 39%, uncertain; and 36%, inappropriate. The panel disagreed about 12% of the therapy indications in the final ratings, falling from 26% in the first-round ratings.
CONCLUSIONS: Key themes emerged from the consensus process. Lacking evidence for a definitive therapy, it was considered most appropriate to enroll eligible patients in clinical trials and refer eligible patients for transplant evaluation. For patients without access to clinical trials, the committee was not unanimous regarding treatment recommendations. It was considered inappropriate for patients with a confident diagnosis of IPF to be treated with corticosteroids as the sole agent: corticosteroids should be used in conjunction with azathioprine. With progressive disease despite such combination use, there was agreement for the use of interferon gamma-1b in patients unwilling or unable to participate in available clinical trials.

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Year:  2005        PMID: 16315778      PMCID: PMC1550766     

Source DB:  PubMed          Journal:  Sarcoidosis Vasc Diffuse Lung Dis        ISSN: 1124-0490            Impact factor:   0.670


  21 in total

1.  Hospital-based historical cohort study of 234 histologically proven Japanese patients with IPF.

Authors:  S Nagai; M Kitaichi; K Hamada; T Nagao; Y Hoshino; H Miki; T Izumi
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  1999-09       Impact factor: 0.670

Review 2.  American Thoracic Society. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS).

Authors: 
Journal:  Am J Respir Crit Care Med       Date:  2000-02       Impact factor: 21.405

3.  Appropriateness of surgery for sciatica: reliability of guidelines from expert panels.

Authors:  J P Vader; F Porchet; T Larequi-Lauber; R W Dubois; B Burnand
Journal:  Spine (Phila Pa 1976)       Date:  2000-07-15       Impact factor: 3.468

4.  Idiopathic pulmonary fibrosis: predicting response to therapy and survival.

Authors:  S E Gay; E A Kazerooni; G B Toews; J P Lynch; B H Gross; P N Cascade; D L Spizarny; A Flint; M A Schork; R I Whyte; J Popovich; R Hyzy; F J Martinez
Journal:  Am J Respir Crit Care Med       Date:  1998-04       Impact factor: 21.405

5.  Treatment of idiopathic pulmonary fibrosis with a new antifibrotic agent, pirfenidone: results of a prospective, open-label Phase II study.

Authors:  G Raghu; W C Johnson; D Lockhart; Y Mageto
Journal:  Am J Respir Crit Care Med       Date:  1999-04       Impact factor: 21.405

6.  A preliminary study of long-term treatment with interferon gamma-1b and low-dose prednisolone in patients with idiopathic pulmonary fibrosis.

Authors:  R Ziesche; E Hofbauer; K Wittmann; V Petkov; L H Block
Journal:  N Engl J Med       Date:  1999-10-21       Impact factor: 91.245

7.  Idiopathic pulmonary fibrosis: Impact of oxygen and colchicine, prednisone, or no therapy on survival.

Authors:  W W Douglas; J H Ryu; D R Schroeder
Journal:  Am J Respir Crit Care Med       Date:  2000-04       Impact factor: 21.405

8.  Colchicine, D-penicillamine, and prednisone in the treatment of idiopathic pulmonary fibrosis: a controlled clinical trial.

Authors:  M Selman; G Carrillo; J Salas; R P Padilla; R Pérez-Chavira; R Sansores; R Chapela
Journal:  Chest       Date:  1998-08       Impact factor: 9.410

9.  Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the Lung Study Group.

Authors:  W W Douglas; J H Ryu; S J Swensen; K P Offord; D R Schroeder; G M Caron; R A DeRemee
Journal:  Am J Respir Crit Care Med       Date:  1998-07       Impact factor: 21.405

10.  Response to steroid therapy in patients of idiopathic pulmonary fibrosis: a retrospective analysis.

Authors:  D Behera; D Gupta; S K Jindal
Journal:  Indian J Chest Dis Allied Sci       Date:  1998 Jul-Sep
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  6 in total

1.  Bleomycin and IL-1beta-mediated pulmonary fibrosis is IL-17A dependent.

Authors:  Mark S Wilson; Satish K Madala; Thirumalai R Ramalingam; Bernadette R Gochuico; Ivan O Rosas; Allen W Cheever; Thomas A Wynn
Journal:  J Exp Med       Date:  2010-02-22       Impact factor: 14.307

Review 2.  Clinical Use of Interferon-gamma.

Authors:  Catriona H T Miller; Stephen G Maher; Howard A Young
Journal:  Ann N Y Acad Sci       Date:  2009-12       Impact factor: 5.691

Review 3.  Idiopathic pulmonary fibrosis.

Authors:  Eric B Meltzer; Paul W Noble
Journal:  Orphanet J Rare Dis       Date:  2008-03-26       Impact factor: 4.123

4.  Chlamydia pneumoniae infection in mice induces chronic lung inflammation, iBALT formation, and fibrosis.

Authors:  Madhulika Jupelli; Kenichi Shimada; Norika Chiba; Anatoly Slepenkin; Randa Alsabeh; Heather D Jones; Ellena Peterson; Shuang Chen; Moshe Arditi; Timothy R Crother
Journal:  PLoS One       Date:  2013-10-25       Impact factor: 3.240

5.  Phase II study of nab-paclitaxel + carboplatin for patients with non-small-cell lung cancer and interstitial lung disease.

Authors:  Hirotsugu Kenmotsu; Kiyotaka Yoh; Keita Mori; Akira Ono; Tomohisa Baba; Yutaka Fujiwara; Ou Yamaguchi; Ryo Ko; Hiroaki Okamoto; Nobuyuki Yamamoto; Takashi Ninomiya; Takashi Ogura; Terufumi Kato
Journal:  Cancer Sci       Date:  2019-11-06       Impact factor: 6.716

6.  The Value of 18F-FDG PET/CT in Evaluating Disease Severity and Prognosis in Idiopathic Pulmonary Fibrosis Patients.

Authors:  Hee-Young Yoon; Suk Hyun Lee; Sejin Ha; Jin-Sook Ryu; Jin Woo Song
Journal:  J Korean Med Sci       Date:  2021-10-25       Impact factor: 2.153

  6 in total

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